Publications by authors named "Mohamed Abdel-Hamid"

100Publications

Radiological evaluations of low cost wollastonite nano-ceramics graft doped with iron oxide in the treatment of induced defects in canine mandible.

Authors:
Mostafa Mabrouk Said K Taha Mohamed A Abdel Hamid Sayed H Kenawy Elham A Hassan Gehan T El-Bassyouni

J Biomed Mater Res B Appl Biomater 2020 Dec 1. Epub 2020 Dec 1.

Refractories, Ceramics and Building Materials Department, National Research Centre, Dokki, Giza, Egypt.

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December 2020

Asparagine Synthetase Deficiency with Intracranial Hemorrhage Can Mimic Molybdenum Cofactor Deficiency.

Authors:
Ghada M H Abdel-Salam Mohamed S Abdel-Hamid

Neuropediatrics 2020 Dec 3. Epub 2020 Dec 3.

Human Genetics and Genome Research Division, Medical Molecular Department, National Research Centre, Cairo, Egypt.

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December 2020

Mutations in Spliceosomal Genes PPIL1 and PRP17 Cause Neurodegenerative Pontocerebellar Hypoplasia with Microcephaly.

Authors:
Guoliang Chai Alice Webb Chen Li Danny Antaki Sangmoon Lee Martin W Breuss Nhi Lang Valentina Stanley Paula Anzenberg Xiaoxu Yang Trevor Marshall Patrick Gaffney Klaas J Wierenga Brian Hon-Yin Chung Mandy Ho-Yin Tsang Lynn S Pais Alysia Kern Lovgren Grace E VanNoy Heidi L Rehm Ghayda Mirzaa Eyby Leon Jullianne Diaz Alexander Neumann Arnout P Kalverda Iain W Manfield David A Parry Clare V Logan Colin A Johnson David T Bonthron Elizabeth M A Valleley Mahmoud Y Issa Sherif F Abdel-Ghafar Mohamed S Abdel-Hamid Patricia Jennings Maha S Zaki Eamonn Sheridan Joseph G Gleeson

Neuron 2020 Nov 17. Epub 2020 Nov 17.

Department of Neurosciences, University of California, San Diego, La Jolla, CA 92093, USA; Rady Children's Institute for Genomic Medicine, San Diego, CA 92130, USA. Electronic address:

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November 2020

Efficacy of Flat-Top Hand-Piece Using 980 nm Diode Laser Photobiomodulation on Socket Healing after Extraction: Split-Mouth Experimental Model in Dogs.

Authors:
Mohamed A Abdel Hamid Amira A Zaied Mohamed Khalifa Zayet Hany Abdelmageed Elham A Hassan Andrea Amaroli

Photochem Photobiol 2020 Nov 15. Epub 2020 Nov 15.

Faculty of Dentistry, Department of Orthopaedic Dentistry, First Moscow State Medical University (Sechenov University), Moscow, Russia.

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November 2020

Blepharophimosis-ptosis-intellectual disability syndrome: A report of nine Egyptian patients with further expansion of phenotypic and mutational spectrum.

Authors:
Maha S Zaki Ghada A Otaify Samira Ismail Mahmoud Y Issa Mona O El-Ruby Abdelrahim A Sadek Engy A Ashaat Sonia A El Saeidi Mona S Aglan Samia Temtamy Mohamed S Abdel-Hamid

Am J Med Genet A 2020 12 19;182(12):2857-2866. Epub 2020 Sep 19.

Medical Molecular Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.

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December 2020

ASAH1-related disorders: Description of 15 novel pediatric patients and expansion of the clinical phenotype.

Authors:
Iman G Mahmoud Mohamed A Elmonem Maha S Zaki Areef Ramadan Nihal M Al-Menabawy Aya El-Gamal Lobna Mansour Mahmoud Y Issa Mohamed S Abdel-Hamid Sawsan Abdel-Hady Iman Khalifa Ahmed Ibrahim Alexander Solyom Arndt Rolfs Laila Selim

Clin Genet 2020 Dec 2;98(6):598-605. Epub 2020 Sep 2.

Pediatrics Department, Neurology and Metabolic division, Faculty of Medicine, Cairo University, Cairo, Egypt.

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December 2020

Two new families with enamel renal syndrome: A novel FAM20A gene mutation and review of literature.

Authors:
Nehal F Hassib Mona A Shoeib Hoda A ElSadek Mona E Wali Mostafa I Mostafa Mohamed S Abdel-Hamid

Eur J Med Genet 2020 Nov 22;63(11):104045. Epub 2020 Aug 22.

Medical Molecular Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt. Electronic address:

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November 2020

Raine syndrome: Prenatal diagnosis based on recognizable fetal facial features and characteristic intracranial calcification.

Authors:
Sara H El-Dessouky Mohamed S Abdel-Hamid Sherif F Abdel-Ghafar Mona M Aboulghar Hassan M Gaafar Mona Fouad Adel H Ahmed Ghada M H Abdel-Salam

Prenat Diagn 2020 12 14;40(12):1578-1597. Epub 2020 Sep 14.

Department of Clinical Genetics, Division of Human Genetics and Genome Research, National Research Centre, Cairo, Egypt.

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December 2020

Micro and Martsolf syndromes in 34 new patients: Refining the phenotypic spectrum and further molecular insights.

Authors:
Mohamed S Abdel-Hamid Sherif F Abdel-Ghafar Suzan R Ismail Lubna M Desouky Mahmoud Y Issa Laila K Effat Maha S Zaki

Clin Genet 2020 Nov;98(5):445-456

Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.

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November 2020

Fluorescence spectroscopy for determination of dapagliflozin in pure form and its tablets formulation; Application to content uniformity testing.

Authors:
Mahmoud A Omar Hytham M Ahmed Hany A Batakoushy Mohamed A Abdel Hamid

Spectrochim Acta A Mol Biomol Spectrosc 2020 Nov 24;241:118642. Epub 2020 Jun 24.

Department of Pharmaceutical Analytical Chemistry, Faculty of Pharmacy, Tanta University, Egypt.

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November 2020

A fast and green reversed-phase HPLC method with fluorescence detection for simultaneous determination of amlodipine and celecoxib in their newly approved fixed-dose combination tablets.

Authors:
Mohamed A Abdel Hamid Mokhtar M Mabrouk Mary A Michael

J Sep Sci 2020 Aug 22;43(16):3197-3205. Epub 2020 Jun 22.

Department of Pharmaceutical Analytical Chemistry, Faculty of Pharmacy, Tanta University, Tanta, Egypt.

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August 2020

Molecular diagnosis in recessive pediatric neurogenetic disease can help reduce disease recurrence in families.

Authors:
Mahmoud Y Issa Zinayida Chechlacz Valentina Stanley Renee D George Jennifer McEvoy-Venneri Denice Belandres Hasnaa M Elbendary Khaled R Gaber Ahmed Nabil Mohamed S Abdel-Hamid Maha S Zaki Joseph G Gleeson

BMC Med Genomics 2020 05 13;13(1):68. Epub 2020 May 13.

Departments of Neurosciences and Pediatrics, Rady Children's Institute for Genomic Medicine, Howard Hughes Medical Institute, University of California San Diego, La Jolla, CA, 92093, USA.

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May 2020

Dose-Dependent Clinical, Radiographic, and Histopathologic Changes of 17β-Estradiol Levels Within the Temporomandibular Joint: An Experimental Study in Ovariectomized Dogs.

Authors:
Mohamed A Abdel Hamid Elham A Hassan Amira A Zaied Andrea Amaroli Nermeen H Sorour

J Oral Maxillofac Surg 2020 Aug 24;78(8):1304-1313. Epub 2020 Mar 24.

Lecturer, Department of Oral and Maxillofacial Surgery, Faculty of Oral and Dental Medicine, Cairo University, Cairo, Egypt.

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August 2020

Microcephalic osteodysplastic primordial dwarfism type II: Additional nine patients with implications on phenotype and genotype correlation.

Authors:
Ghada M H Abdel-Salam Inas S M Sayed Hanan H Afifi Sherif F Abdel-Ghafar Maha R Abouzaid Samira I Ismail Mona S Aglan Mahmoud Y Issa Hala T El-Bassyouni Ghada El-Kamah Laila K Effat Maha Eid Maha S Zaki Samia A Temtamy Mohamed S Abdel-Hamid

Am J Med Genet A 2020 06 8;182(6):1407-1420. Epub 2020 Apr 8.

Centre of Excellence for Human Genetics, National Research Centre, Cairo, Egypt.

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June 2020

New spectrofluorimetric analysis of empagliflozin in its tablets and human plasma using two level full factorial design.

Authors:
Mahmoud A Omar Hytham M Ahmed Hany A Batakoushy Mohamed A Abdel Hamid

Spectrochim Acta A Mol Biomol Spectrosc 2020 Jul 26;235:118307. Epub 2020 Mar 26.

Department of Pharmaceutical Analytical Chemistry, Faculty of Pharmacy, Tanta University, Egypt.

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July 2020

KBG syndrome in two patients from Egypt.

Authors:
Inas S M Sayed Mohamed S Abdel-Hamid Ghada M H Abdel-Salam

Am J Med Genet A 2020 06 28;182(6):1309-1312. Epub 2020 Mar 28.

Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.

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June 2020

Comparison Between Silicone Oil and Gas in Tamponading Giant Retinal Breaks.

Authors:
Hossam Mohamed Moharram Ahmed Shawkat Abdelhalim Mohamed Abdel Hamid Mohamed Farouk Abdelkader

Clin Ophthalmol 2020 15;14:127-132. Epub 2020 Jan 15.

Department of Ophthalmology, Faculty of Medicine, Minia University, Minia, Egypt.

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January 2020

Evaluation of Pesticide Residues in Vegetables from the Asir Region, Saudi Arabia.

Authors:
Mohamed F A Ramadan Mohamed M A Abdel-Hamid Montasser M F Altorgoman Hamed A AlGaramah Mohammed A Alawi Ali A Shati Hoda A Shweeta Nasser S Awwad

Molecules 2020 Jan 3;25(1). Epub 2020 Jan 3.

Research Centre for Advanced Materials Science (RCAMS), King Khalid University, P.O. Box 9004, Abha 61413, Saudi Arabia.

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January 2020

Second-derivative synchronous spectrofluorimetric assay of dapagliflozin: Application to stability study and pharmaceutical preparation.

Authors:
Mahmoud A Omar Mohamed A Abdel Hamid Hany A Batakoushy Hytham M Ahmed

Luminescence 2020 Mar 15;35(2):260-265. Epub 2019 Nov 15.

Pharmaceutical Analysis Department, Faculty of Pharmacy, Menoufia University, Egypt.

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March 2020

Bilateral Calcification of Basal Ganglia in a Patient with Duplication of Both 11q13.1q22.1 and 4q35.2 with New Phenotypic Features.

Authors:
Maha S Zaki Ola M Eid Maha M Eid Amal M Mohamed Inas S M Sayed Mohamed S Abdel-Hamid Ghada M H Abdel-Salam

Cytogenet Genome Res 2019 13;159(3):130-136. Epub 2019 Nov 13.

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February 2020

Lenz-Majewski syndrome in a patient from Egypt.

Authors:
Hanan H Afifi Mohamed S Abdel-Hamid Mennat I Mehrez Ghada El-Kamah Ghada M H Abdel-Salam

Am J Med Genet A 2019 10 12;179(10):2039-2042. Epub 2019 Aug 12.

Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.

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October 2019

Phenotypic and mutational spectrum of thirty-five patients with Sjögren-Larsson syndrome: identification of eleven novel ALDH3A2 mutations and founder effects.

Authors:
Mohamed S Abdel-Hamid Mahmoud Y Issa Hasnaa M Elbendary Sherif F Abdel-Ghafar Karima Rafaat Heba Hosny Marian Girgis Ghada M H Abdel-Salam Maha S Zaki

J Hum Genet 2019 Sep 5;64(9):859-865. Epub 2019 Jul 5.

Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.

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September 2019

New spectrofluorimetric analysis of dapagliflozin after derivatization with NBD-Cl in human plasma using factorial design experiments.

Authors:
Mahmoud A Omar Hytham M Ahmed Mohamed A Abdel Hamid Hany A Batakoushy

Luminescence 2019 Sep 29;34(6):576-584. Epub 2019 Apr 29.

Pharmaceutical Analysis Department, Faculty of Pharmacy, Menoufia University, Egypt.

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September 2019

Phenotypic spectrum of NDE1-related disorders: from microlissencephaly to microhydranencephaly.

Authors:
Mohamed S Abdel-Hamid Sara H El-Dessouky Mohamed I Ateya Hassan M Gaafar Ghada M H Abdel-Salam

Am J Med Genet A 2019 03 13;179(3):494-497. Epub 2019 Jan 13.

Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.

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March 2019

GAPO syndrome in seven new patients: Identification of five novel ANTXR1 mutations including the first large intragenic deletion.

Authors:
Mohamed S Abdel-Hamid Samira Ismail Maha S Zaki Ghada M H Abdel-Salam Ghada A Otaify Mahmoud Y Issa Mohamed Abdel-Kader Marian Girgis Eman Aboul-Ezz Inas Mazen Mona S Aglan Samia A Temtamy

Am J Med Genet A 2019 02 21;179(2):237-242. Epub 2018 Dec 21.

Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.

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February 2019

Rectal vs. sublingual misoprostol before cesarean section: double-blind, three-arm, randomized clinical trial.

Authors:
Mohamed S Sweed Mourad M El-Saied Amgad E Abou-Gamrah Haitham A El-Sabaa Mohamed M Abdel-Hamid Hossam Hemeda Ahmed M Mansour Mohamed E Shawky Medhat A El-Sayed Radwa M Mohamed

Arch Gynecol Obstet 2018 12 5;298(6):1115-1122. Epub 2018 Oct 5.

Obstetrics and Gynecology Department, Ain Shams University, Cairo, 16646, Egypt.

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December 2018

Phenotypic and molecular insights into PQBP1-related intellectual disability.

Authors:
Ghada M H Abdel-Salam Noriko Miyake Mohamed S Abdel-Hamid Inas S M Sayed Mohamed I Gadelhak Samira I Ismail Mona S Aglan Hanan H Afifi Samia A Temtamy Naomichi Matsumoto

Am J Med Genet A 2018 11 23;176(11):2446-2450. Epub 2018 Sep 23.

Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.

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November 2018

Analysis of Hepatitis B virus (HBV) mutations in patients from Western Saudi Arabia with chronic disease.

Authors:
Sherif Aly El-Kafrawy Ghazi Abdulatif Jamjoom Hisham Othman Akbar Hind Ibrahim Baker Fallatah Mai Mohamed El-Daly Yousef Abdulfattah Qari Abdullah Saeed Alghamdi Mohamed Babatin Mohammed Abdullah Alsaedi Noura Abdulhamid Othman Tagreed Lafi Al-Subhi Mohamed Abdel-Hamid Esam Ibraheem Azhar

J Infect Dev Ctries 2018 Jul 31;12(7):557-567. Epub 2018 Jul 31.

King Abdulaziz University, Jeddah, Saudi Arabia.

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July 2018

Study of the Humoral Immune Response towards HCV Genotype 4 Using a Bead-Based Multiplex Serological Assay.

Authors:
Angela Filomena Jens C Göpfert Darragh Duffy Stanislas Pol Mohamed Abdel-Hamid Gamal Esmat Arnaud Fontanet Matthew L Albert Thomas O Joos Nicole Schneiderhan-Marra

High Throughput 2017 Oct 30;6(4). Epub 2017 Oct 30.

NMI Natural and Medical Sciences Institute at the University of Tuebingen, 72770 Reutlingen, Germany.

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October 2017

Early application of haemostatic powder added to standard management for oesophagogastric variceal bleeding: a randomised trial.

Authors:
Mostafa Ibrahim Ahmed El-Mikkawy Mohamed Abdel Hamid Haitham Abdalla Arnaud Lemmers Ibrahim Mostafa Jacques Devière

Gut 2019 05 5;68(5):844-853. Epub 2018 May 5.

Department of Gastroenterology, Hepatopancreatology and Digestive Oncology, Erasme Hospital, Université Libre de Bruxelles, Brussels, Belgium.

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May 2019

Identification of a novel homozygous ALX4 mutation in two unrelated patients with frontonasal dysplasia type-2.

Authors:
Mona El-Ruby Alaa El-Din Fayez Sara H El-Dessouky Mona S Aglan Inas Mazen Nora Ismail Hanan H Afifi Maha M Eid Mostafa I Mostafa Mennat I Mehrez Yasmin Khalil Maha S Zaki Khaled R Gaber Mohamed S Abdel-Hamid Ghada M H Abdel-Salam

Am J Med Genet A 2018 05;176(5):1190-1194

Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.

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May 2018

Aromatase Deficiency due to a Homozygous CYP19A1 Mutation in a 46,XX Egyptian Patient with Ambiguous Genitalia.

Authors:
Inas Mazen Ken McElreavey Aya Elaidy Alaa K Kamel Mohamed S Abdel-Hamid

Sex Dev 2017 12;11(5-6):275-279. Epub 2018 Jan 12.

Department of Clinical Genetics, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.

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October 2018

Genetic Susceptibility in Family Members of Egyptian Hepatitis C Virus Infected Patients: Role of Interleukin-12 B Gene Polymorphism.

Authors:
Nadia Elwan Fathia Assal Asem Elfert Lobna AboAli Shaimaa Soliman Samah Soliman Walaa Elkhalawany Rehab Badawy Laila Effat Khalda Sayed Safinaz Shalaby Marwa Shehab Mohamed Abdel-Hamid Sherief Abd-Elsalam

Infect Disord Drug Targets 2019 ;19(1):81-87

Departments of Tropical Medicine and Public Health, Faculty of Medicine, Tanta University, El- Giash Street 31111, Tanta, Egypt.

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June 2019

Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation.

Authors:
Ghada M H Abdel-Salam Mohamed S Abdel-Hamid Mennat I Mehrez Ahmad M Kamal Mohamed B Taher Hanan H Afifi

Ophthalmic Genet 2018 04 15;39(2):215-220. Epub 2017 Nov 15.

a Clinical Genetics Department, Human Genetics and Genome Research Division , National Research Centre , Cairo , Egypt.

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April 2018

Effectiveness of ravidasvir plus sofosbuvir in interferon-naïve and treated patients with chronic hepatitis C genotype-4.

Authors:
Gamal Esmat Tamer Elbaz Maissa El Raziky Asmaa Gomaa Mahmoud Abouelkhair Hadeel Gamal El Deen Aliaa Sabry Mohamed Ashour Naglaa Allam Mohamed Abdel-Hamid Ola Nada Sherine Helmy Hanaa Abdel-Maguid Richard Colonno Nathaniel Brown Eric Ruby Pamela Vig Imam Waked

J Hepatol 2017 Sep 19. Epub 2017 Sep 19.

National Liver Institute, Menoufiya University, Shebeen EL Kom, Egypt. Electronic address:

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September 2017

Comparative Pharmacokinetic Study for Linezolid and Two Novel Antibacterial Oxazolidinone Derivatives in Rabbits: Can Differences in the Pharmacokinetic Properties Explain the Discrepancies between Their In Vivo and In Vitro Antibacterial Activities?

Authors:
Mohsen A Hedaya Vidhya Thomas Mohamed E Abdel-Hamid Elijah O Kehinde Oludotun A Phillips

Pharmaceutics 2017 Sep 7;9(3). Epub 2017 Sep 7.

Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Kuwait University, P.O. Box 24923, Safat 13110, Kuwait.

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September 2017

Correlation between hepatitis C viral load and hepatitis C Core antigenaemia among Egyptians.

Authors:
Dalia N Kotb Mona A Esmail Sayed F Abdelwahab Mohamed Abdel-Hamid

East Mediterr Health J 2017 Jun 14;23(4):280-286. Epub 2017 Jun 14.

Department of Microbiology and Immunology, Faculty of Medicine, Minia University, Minia, Egypt.

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June 2017

Genetic mutation in Egyptian children with steroid-resistant nephrotic syndrome.

Authors:
Manal Micheal Thomas Mohamed S Abdel-Hamid Nermine Nabil Mahfouz Emad Emil Ghobrial

J Formos Med Assoc 2018 Jan 3;117(1):48-53. Epub 2017 Apr 3.

Kasr Al Ainy School of Medicine, Cairo University, Cairo, Egypt.

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January 2018

Aicardi-Goutières syndrome: unusual neuro-radiological manifestations.

Authors:
Ghada M H Abdel-Salam Mohamed S Abdel-Hamid Shaimaa A Mohammad Sherif F Abdel-Ghafar Doaa R Soliman Hala T El-Bassyouni Laila Effat Maha S Zaki

Metab Brain Dis 2017 06 23;32(3):679-683. Epub 2017 Mar 23.

Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.

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June 2017

Design of novel injectable in-situ forming scaffolds for non-surgical treatment of periapical lesions: In-vitro and in-vivo evaluation.

Authors:
Rehab N Shamma Nermeen A Elkasabgy Azza A Mahmoud Shaimaa I Gawdat Mohamed M Kataia Mohamed A Abdel Hamid

Int J Pharm 2017 Apr 21;521(1-2):306-317. Epub 2017 Feb 21.

Department of Surgery, Anaesthiology and Radiology, Faculty of Veterinary Medicine, Cairo University, Cairo, Egypt.

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April 2017

A novel frameshift mutation in the sterol 27-hydroxylase gene in an Egyptian family with cerebrotendinous xanthomatosis without cataract.

Authors:
Mohamed S Abdel-Hamid Mahmoud Y Issa Ghada A Otaify Maha S Zaki

Metab Brain Dis 2017 04 22;32(2):311-315. Epub 2017 Feb 22.

Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Tahrir street, Dokki, Giza, Cairo, 12311, Egypt.

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April 2017

Band-like calcification with simplified gyration and polymicrogyria: report of 10 new families and identification of five novel OCLN mutations.

Authors:
Mohamed S Abdel-Hamid Ghada M H Abdel-Salam Mahmoud Y Issa Bayoumi A Emam Maha S Zaki

J Hum Genet 2017 Apr 9;62(5):553-559. Epub 2017 Feb 9.

Division of Human Genetics and Genome Research, Department of Clinical Genetics, National Research Centre, Cairo, Egypt.

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April 2017

Novel AMH and AMHR2 Mutations in Two Egyptian Families with Persistent Müllerian Duct Syndrome.

Authors:
Inas Mazen Mona El-Gammal Ken McElreavey Aya Elaidy Mohamed S Abdel-Hamid

Sex Dev 2017 1;11(1):29-33. Epub 2017 Feb 1.

Department of Clinical Genetics, Human Genetic and Genome Research Division, National Research Centre, Cairo, Egypt.

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November 2017

Molecular and clinical analysis of ALPL in a cohort of patients with suspicion of Hypophosphatasia.

Authors:
Jair Tenorio Ignacio Álvarez Leyre Riancho-Zarrabeitia Gabriel Á Martos-Moreno Giorgia Mandrile Monserrat de la Flor Crespo Mikhail Sukchev Mostafa Sherif Iza Kramer María T Darnaude-Ortiz Pedro Arias Gema Gordo Irene Dapía Julián Martinez-Villanueva Rubén Gómez José Manuel Iturzaeta Ghada Otaify Mayte García-Unzueta Alessandro Rubinacci José A Riancho Mona Aglan Samia Temtamy Mohamed Abdel Hamid Jesús Argente Víctor L Ruiz-Pérez Karen E Heath Pablo Lapunzina

Am J Med Genet A 2017 Mar 27;173(3):601-610. Epub 2017 Jan 27.

Institute of Medical and Molecular Genetics (INGEMM), Hospital Universitario La Paz, IdiPAZ, Universidad Autónoma de Madrid, Madrid, Spain.

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March 2017

Genetic polymorphisms of human cytochrome P450 CYP1A1 in an Egyptian population and tobacco-induced lung cancer.

Authors:
Nada Ezzeldin Dalia El-Lebedy Amira Darwish Ahmed El-Bastawisy Mirhane Hassan Shereen Abd El-Aziz Mohamed Abdel-Hamid Amal Saad-Hussein

Genes Environ 2017 7;39. Epub 2017 Jan 7.

Department of Environmental Health and Preventive Medicine, National Research Center, Cairo, Egypt.

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January 2017

Effect of Diabetea tea ™ consumption on inflammatory cytokines and metabolic biomarkers in type 2 diabetes patients.

Authors:
Fadia Mahmoud Ebaa Al-Ozairi David Haines Ladislav Novotny Ali Dashti Basel Ibrahim Mohamed Abdel-Hamid

J Ethnopharmacol 2016 Dec 27;194:1069-1077. Epub 2016 Oct 27.

Faculty of Pharmacy, Department of Pharmacology, University of Debrecen, Debrecen, Hungary. Electronic address:

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December 2016

A validated UPLC-MS/MS method for the analysis of linezolid and a novel oxazolidinone derivative (PH027) in plasma and its application to tissue distribution study in rabbits.

Authors:
Mohsen A Hedaya Vidhya Thomas Mohamed E Abdel-Hamid Elijah O Kehinde Oludotun A Phillips

J Chromatogr B Analyt Technol Biomed Life Sci 2017 Jan 27;1040:89-96. Epub 2016 Nov 27.

Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Kuwait University, P.O. Box 24923, Safat 13110, Kuwait. Electronic address:

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January 2017

Environmental, maternal, and reproductive risk factors for childhood acute lymphoblastic leukemia in Egypt: a case-control study.

Authors:
Sameera Ezzat Wafaa M Rashed Sherin Salem M Tevfik Dorak Mai El-Daly Mohamed Abdel-Hamid Iman Sidhom Alaa El-Hadad Christopher Loffredo

BMC Cancer 2016 08 20;16:662. Epub 2016 Aug 20.

Lombardi Cancer Center, Georgetown University, Washington, DC, USA.

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August 2016

Diagnostic accuracy of the γ-glutamyl transpeptidase to platelet ratio to predict liver fibrosis in Egyptian patients with HCV genotype 4.

Authors:
Yusuke Shimakawa Philippe Bonnard Mohamed El Kassas Mohamed Abdel-Hamid Gamal Esmat Arnaud Fontanet

Gut 2016 09 7;65(9):1577-8. Epub 2016 Jul 7.

Unité d'Épidémiologie des Maladies Émergentes, Institut Pasteur, Paris, France Département d'Infection et Epidémiologie, Conservatoire National des Arts et Métiers, Paris, France.

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September 2016

Megalencephalic leukoencephalopathy with cysts in twelve Egyptian patients: novel mutations in MLC1 and HEPACAM and a founder effect.

Authors:
Ghada M H Abdel-Salam Mohamed S Abdel-Hamid Samira I Ismail Heba Hosny Tarek Omar Laila Effat Mona S Aglan Samia A Temtamy Maha S Zaki

Metab Brain Dis 2016 10 7;31(5):1171-9. Epub 2016 Jul 7.

Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Tahrir street, Dokki, Cairo, Egypt.

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October 2016

Molybdenum cofactor and isolated sulphite oxidase deficiencies: Clinical and molecular spectrum among Egyptian patients.

Authors:
Maha S Zaki Laila Selim Hala T El-Bassyouni Mahmoud Y Issa Iman Mahmoud Samira Ismail Mariane Girgis Abdelrahim A Sadek Joseph G Gleeson Mohamed S Abdel Hamid

Eur J Paediatr Neurol 2016 Sep 30;20(5):714-22. Epub 2016 May 30.

Medical Molecular Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo 12311, Egypt.

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September 2016

Molecular and phenotypic spectrum of ASPM-related primary microcephaly: Identification of eight novel mutations.

Authors:
Mohamed S Abdel-Hamid Manal F Ismail Hebatallh A Darwish Laila K Effat Maha S Zaki Ghada M H Abdel-Salam

Am J Med Genet A 2016 08 2;170(8):2133-40. Epub 2016 Jun 2.

Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.

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August 2016

Identification of NR5A1 Mutations and Possible Digenic Inheritance in 46,XY Gonadal Dysgenesis.

Authors:
Inas Mazen Mohamed Abdel-Hamid Mona Mekkawy Joëlle Bignon-Topalovic Radia Boudjenah Mona El Gammal Mona Essawi Anu Bashamboo Ken McElreavey

Sex Dev 2016 12;10(3):147-51. Epub 2016 May 12.

Department of Clinical Genetics, National Research Center, Cairo, Egypt.

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November 2017

PYCR2 Mutations cause a lethal syndrome of microcephaly and failure to thrive.

Authors:
Maha S Zaki Gifty Bhat Tipu Sultan Mahmoud Issa Hea-Jin Jung Esra Dikoglu Laila Selim Imam G Mahmoud Mohamed S Abdel-Hamid Ghada Abdel-Salam Isaac Marin-Valencia Joseph G Gleeson

Ann Neurol 2016 07 1;80(1):59-70. Epub 2016 Jun 1.

Laboratory for Pediatric Brain Disease, Howard Hughes Medical Institute, Rockefeller University, New York, NY.

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July 2016

Excess mortality rate associated with hepatitis C virus infection: A community-based cohort study in rural Egypt.

Authors:
Aya Mostafa Yusuke Shimakawa Ahmed Medhat Nabiel N Mikhail Cédric B Chesnais Naglaa Arafa Iman Bakr Mostafa El Hoseiny Mai El-Daly Gamal Esmat Mohamed Abdel-Hamid Mostafa K Mohamed Arnaud Fontanet

J Hepatol 2016 06 26;64(6):1240-6. Epub 2016 Feb 26.

Unité d'Épidémiologie des Maladies Émergentes, Institut Pasteur, Paris, France; Département d'Infection et Épidémiologie, Conservatoire National des Arts et Métiers, Paris, France. Electronic address:

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June 2016

De Novo Mutation in ABCC9 Causes Hypertrichosis Acromegaloid Facial Features Disorder.

Authors:
Hanan H Afifi Mohamed S Abdel-Hamid Maha M Eid Inas S Mostafa Ghada M H Abdel-Salam

Pediatr Dermatol 2016 Mar-Apr;33(2):e109-13. Epub 2016 Feb 12.

Clinical Genetics Department, National Research Centre, Cairo, Egypt.

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January 2017

Occult hepatitis C virus infection among Egyptian hemodialysis patients.

Authors:
Soha S Abdelrahim Rasha Khairy Mona Abdel-Monem Esmail Mahmoud Ragab Mohamed Abdel-Hamid Sayed F Abdelwahab

J Med Virol 2016 08 18;88(8):1388-93. Epub 2016 Jan 18.

Department of Microbiology and Immunology, Faculty of Medicine, Minia University, Minia, Egypt.

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August 2016

Injectable nanoamorphous calcium phosphate based in situ gel systems for the treatment of periapical lesions.

Authors:
Amany A Mostafa Mohamed H Zaazou Laurence C Chow Azza A Mahmoud Dalia Y Zaki Mona Basha Mohamed A Abdel Hamid Maram E Khallaf Nehal F Sharaf Tamer M Hamdy

Biomed Mater 2015 Nov 6;10(6):065006. Epub 2015 Nov 6.

Biomaterials Department, National Research Centre (NRC), El Bohouth St., 12622 Dokki, Cairo, Egypt. Nanomedicine & Tissue Engineering Laboratory, Medical Research Center of Excellence (MRCE), NRC, Cairo, Egypt.

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November 2015

Viral transmission risk factors in an Egyptian population with high hepatitis C prevalence.

Authors:
Mary Kate Mohlman Doa'a A Saleh Sameera Ezzat Mohamed Abdel-Hamid Brent Korba Kirti Shetty Sania Amr Christopher A Loffredo

BMC Public Health 2015 Oct 7;15:1030. Epub 2015 Oct 7.

Lombardi Cancer Center, Georgetown University, 3970 Reservoir Rd, Washington, DC, 20057, USA.

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October 2015

Long-term survival in microcephalic osteodysplastic primordial dwarfism type I: Evaluation of an 18-year-old male with g.55G>A homozygous mutation in RNU4ATAC.

Authors:
Ghada M H Abdel-Salam Bayoumi A Emam Yasmin M Khalil Mohamed S Abdel-Hamid

Am J Med Genet A 2016 Jan 30;170A(1):277-82. Epub 2015 Sep 30.

Department of Medical Molecular Genetics, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.

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January 2016

Mutation in WDR4 impairs tRNA m(7)G46 methylation and causes a distinct form of microcephalic primordial dwarfism.

Authors:
Ranad Shaheen Ghada M H Abdel-Salam Michael P Guy Rana Alomar Mohamed S Abdel-Hamid Hanan H Afifi Samira I Ismail Bayoumi A Emam Eric M Phizicky Fowzan S Alkuraya

Genome Biol 2015 Sep 28;16:210. Epub 2015 Sep 28.

Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

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September 2015

Clinical and molecular characterization of seven Egyptian families with autosomal recessive robinow syndrome: Identification of four novel ROR2 gene mutations.

Authors:
Mona Aglan Khalda Amr Samira Ismail Adel Ashour Ghada A Otaify Mennat Allah I Mehrez Eman H A Aboul-Ezz Mona El-Ruby Inas Mazen Mohamed S Abdel-Hamid Samia A Temtamy

Am J Med Genet A 2015 Dec 18;167A(12):3054-61. Epub 2015 Aug 18.

Department of Clinical Genetics, Division of Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.

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December 2015

Polymorphisms at IL28B gene as predictors of viral relapse in genotype 4 Egyptian hepatitis C patients.

Authors:
Mona Abdelmonem Esmail Noha A Hassuna Khalda Sayed Amr Eman Ramadan Ghazawy Mohamed Abdel-Hamid

J Med Virol 2016 Mar 26;88(3):481-6. Epub 2015 Aug 26.

Microbiology and Immunology Department, Faculty of Medicine, Minia University, Egypt.

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March 2016

Refined association of melanoma differentiation-associated gene 5 variants with spontaneous hepatitis C virus clearance in Egypt.

Authors:
Vincent Pedergnana Mohamed Abdel-Hamid Julien Guergnon Ioannis Theodorou Arnaud Fontanet Laurent Abel Aurélie Cobat

Hepatology 2016 Mar 4;63(3):1059-61. Epub 2015 Aug 4.

Laboratory of Human Genetics of Infectious Diseases, Necker Branch Institut National de la Santé et de la Recherche Médicale U1163, Paris, France.

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March 2016

Fetal brain disruption sequence versus fetal brain arrest: A distinct autosomal recessive developmental brain malformation phenotype.

Authors:
Ghada M H Abdel-Salam Mohamed S Abdel-Hamid Hamed A El-Khayat Ola M Eid Soliman Saba Mona K Farag Sahar N Saleem Khaled R Gaber

Am J Med Genet A 2015 May 10;167A(5):1089-99. Epub 2015 Mar 10.

Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.

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May 2015

Evaluating the association of APOA2 polymorphism with insulin resistance in adolescents.

Authors:
Moushira Erfan Zaki Khalda Sayed Amr Mohamed Abdel-Hamid

Meta Gene 2014 Dec 15;2:366-73. Epub 2014 May 15.

Medical Molecular Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Egypt.

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December 2014

Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1.

Authors:
Yanick J Crow Diana S Chase Johanna Lowenstein Schmidt Marcin Szynkiewicz Gabriella M A Forte Hannah L Gornall Anthony Oojageer Beverley Anderson Amy Pizzino Guy Helman Mohamed S Abdel-Hamid Ghada M Abdel-Salam Sam Ackroyd Alec Aeby Guillermo Agosta Catherine Albin Stavit Allon-Shalev Montse Arellano Giada Ariaudo Vijay Aswani Riyana Babul-Hirji Eileen M Baildam Nadia Bahi-Buisson Kathryn M Bailey Christine Barnerias Magalie Barth Roberta Battini Michael W Beresford Geneviève Bernard Marika Bianchi Thierry Billette de Villemeur Edward M Blair Miriam Bloom Alberto B Burlina Maria Luisa Carpanelli Daniel R Carvalho Manuel Castro-Gago Anna Cavallini Cristina Cereda Kate E Chandler David A Chitayat Abigail E Collins Concepcion Sierra Corcoles Nuno J V Cordeiro Giovanni Crichiutti Lyvia Dabydeen Russell C Dale Stefano D'Arrigo Christian G E L De Goede Corinne De Laet Liesbeth M H De Waele Ines Denzler Isabelle Desguerre Koenraad Devriendt Maja Di Rocco Michael C Fahey Elisa Fazzi Colin D Ferrie António Figueiredo Blanca Gener Cyril Goizet Nirmala R Gowrinathan Kalpana Gowrishankar Donncha Hanrahan Bertrand Isidor Bülent Kara Nasaim Khan Mary D King Edwin P Kirk Ram Kumar Lieven Lagae Pierre Landrieu Heinz Lauffer Vincent Laugel Roberta La Piana Ming J Lim Jean-Pierre S-M Lin Tarja Linnankivi Mark T Mackay Daphna R Marom Charles Marques Lourenço Shane A McKee Isabella Moroni Jenny E V Morton Marie-Laure Moutard Kevin Murray Rima Nabbout Sheela Nampoothiri Noemi Nunez-Enamorado Patrick J Oades Ivana Olivieri John R Ostergaard Belén Pérez-Dueñas Julie S Prendiville Venkateswaran Ramesh Magnhild Rasmussen Luc Régal Federica Ricci Marlène Rio Diana Rodriguez Agathe Roubertie Elisabetta Salvatici Karin A Segers Gyanranjan P Sinha Doriette Soler Ronen Spiegel Tommy I Stödberg Rachel Straussberg Kathryn J Swoboda Mohnish Suri Uta Tacke Tiong Y Tan Johann te Water Naude Keng Wee Teik Maya Mary Thomas Marianne Till Davide Tonduti Enza Maria Valente Rudy Noel Van Coster Marjo S van der Knaap Grace Vassallo Raymon Vijzelaar Julie Vogt Geoffrey B Wallace Evangeline Wassmer Hannah J Webb William P Whitehouse Robyn N Whitney Maha S Zaki Sameer M Zuberi John H Livingston Flore Rozenberg Pierre Lebon Adeline Vanderver Simona Orcesi Gillian I Rice

Am J Med Genet A 2015 Feb 16;167A(2):296-312. Epub 2015 Jan 16.

INSERM UMR 1163, Laboratory of Neurogenetics and Neuroinflammation, Paris Descartes - Sorbonne Paris Cité University, Institut Imagine, Hôpital Necker, Paris, France; Manchester Centre for Genomic Medicine, Institute of Human Development, Faculty of Medical and Human Sciences, Manchester Academic Health Sciences Centre, University of Manchester, Manchester, UK.

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February 2015

Hepatitis C virus acquisition among Egyptians: analysis of a 10-year surveillance of acute hepatitis C.

Authors:
Amira Mohsen Adeline Bernier Lenaig LeFouler Elisabeth Delarocque-Astagneau Mai El-Daly Sherif El-Kafrawy Salwa El-Mango Mohamed Abdel-Hamid Mohsen Gadallah Gamal Esmat Mostafa K Mohamed Arnaud Fontanet

Trop Med Int Health 2015 Jan 22;20(1):89-97. Epub 2014 Oct 22.

Community Medicine Department, National Research Center, Cairo, Egypt.

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January 2015

Effect of preventive and curative interventions on hepatitis C virus transmission in Egypt (ANRS 1211): a modelling study.

Authors:
Romulus Breban Naglaa Arafa Sandrine Leroy Aya Mostafa Iman Bakr Laura Tondeur Mohamed Abdel-Hamid Wahid Doss Gamal Esmat Mostafa K Mohamed Arnaud Fontanet

Lancet Glob Health 2014 Sep 27;2(9):e541-e549. Epub 2014 Aug 27.

Institut Pasteur, Emerging Diseases Epidemiology Unit, Paris, France; Conservatoire National des Arts et Métiers, Paris, France.

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September 2014

Mutations in ADAR1, IFIH1, and RNASEH2B presenting as spastic paraplegia.

Authors:
Yanick J Crow Maha S Zaki Mohamed S Abdel-Hamid Ghada Abdel-Salam Odile Boespflug-Tanguy Nuno J V Cordeiro Joseph G Gleeson Nirmala Rani Gowrinathan Vincent Laugel Florence Renaldo Diana Rodriguez John H Livingston Gillian I Rice

Neuropediatrics 2014 Dec 22;45(6):386-93. Epub 2014 Sep 22.

Manchester Academic Health Science Centre, University of Manchester, Genetic Medicine, Manchester, United Kingdom.

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December 2014

A novel mutation (c.2735_2736delTC) in the androgen receptor gene in 46,XY females with complete androgen insensitivity syndrome in an Egyptian family.

Authors:
Inas Mazen Hala Soliman Mona El-Gammal Ahmed Torky Mona Mekkawy Mohamed S Abdel-Hamid Mona Essawi

Horm Res Paediatr 2014 16;82(6):411-4. Epub 2014 Jul 16.

Department of Clinical Genetics, National Research Centre, Cairo, Egypt.

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October 2015

Apolipoprotein H expression is associated with IL28B genotype and viral clearance in hepatitis C virus infection.

Authors:
Melissa E Laird Amira Mohsen Darragh Duffy Rasha Mamdouh Lenaig LeFouler Armanda Casrouge Mai El-Daly Mona Rafik Mohamed Abdel-Hamid Alexandre Soulier Jean-Michel Pawlotsky Christophe Hézode Isabelle Rosa Philippe Renard Mostafa K Mohamed Philippe Bonnard Jacques Izopet Vincent Mallet Stanislas Pol Matthew L Albert Arnaud Fontanet

J Hepatol 2014 Oct 4;61(4):770-6. Epub 2014 Jun 4.

Emerging Disease Epidemiology Unit, Institut Pasteur, Paris, France; Conservatoire National des Arts et Métiers, Paris, France. Electronic address:

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October 2014

Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia in four Egyptian families: report of three novel mutations in the vitamin D receptor gene.

Authors:
Inas Mazen Samira Ismail Khalda Amr Mona El Gammal Mohamed Abdel-Hamid

J Pediatr Endocrinol Metab 2014 Sep;27(9-10):873-8

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September 2014

The ABCs of viral hepatitis that define biomarker signatures of acute viral hepatitis.

Authors:
Darragh Duffy Rasha Mamdouh Melissa Laird Charlotte Soneson Lenaig Le Fouler Maï El-Daly Armanda Casrouge Jérémie Decalf Amal Abbas Noha Sharaf Eldin Magnus Fontes Mohamed Abdel-Hamid Mostafa K Mohamed Mona Rafik Arnaud Fontanet Matthew L Albert

Hepatology 2014 Apr 18;59(4):1273-82. Epub 2014 Feb 18.

Laboratory of Dendritic Cells Immunobiology, Institut Pasteur, Paris, France; INSERM U818, Paris, France.

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April 2014

A novel method to identify routes of hepatitis C virus transmission.

Authors:
Cyrille Féray Julie Bouscaillou Bruno Falissard Mostafa K Mohamed Naglaa Arafa Iman Bakr Mostafa El-Hoseiny Mai El Daly Sherif El-Kafrawy Sabine Plancoulaine Mohamed Abdel-Hamid Valérie Thiers Arnaud Fontanet

PLoS One 2014 23;9(1):e86098. Epub 2014 Jan 23.

Institut Pasteur, Unité d'Epidémiologie des Maladies Emergentes, Paris, France ; Conservatoire National des Arts et Métiers, Chaire Santé et Développement, Paris, France.

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November 2014

APOA2 Polymorphism in Relation to Obesity and Lipid Metabolism.

Authors:
Moushira Erfan Zaki Khalda Sayed Amr Mohamed Abdel-Hamid

Cholesterol 2013 9;2013:289481. Epub 2013 Dec 9.

Human Genetics and Genome Research Division, Medical Molecular Genetics Department, National Research Centre, Cairo 12622, Egypt.

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January 2014

Pesticides, gene polymorphisms, and bladder cancer among Egyptian agricultural workers.

Authors:
Sania Amr Rebecca Dawson Doa'a A Saleh Laurence S Magder Diane Marie St George Mai El-Daly Katherine Squibb Nabiel N Mikhail Mohamed Abdel-Hamid Hussein Khaled Christopher A Loffredo

Arch Environ Occup Health 2015 ;70(1):19-26

a Department of Epidemiology and Public Health , University of Maryland School of Medicine , Baltimore , Maryland , USA.

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February 2015

Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study.

Authors:
Gillian I Rice Gabriella M A Forte Marcin Szynkiewicz Diana S Chase Alec Aeby Mohamed S Abdel-Hamid Sam Ackroyd Rebecca Allcock Kathryn M Bailey Umberto Balottin Christine Barnerias Genevieve Bernard Christine Bodemer Maria P Botella Cristina Cereda Kate E Chandler Lyvia Dabydeen Russell C Dale Corinne De Laet Christian G E L De Goede Mireia Del Toro Laila Effat Noemi Nunez Enamorado Elisa Fazzi Blanca Gener Madli Haldre Jean-Pierre S-M Lin John H Livingston Charles Marques Lourenco Wilson Marques Patrick Oades Pärt Peterson Magnhild Rasmussen Agathe Roubertie Johanna Loewenstein Schmidt Stavit A Shalev Rogelio Simon Ronen Spiegel Kathryn J Swoboda Samia A Temtamy Grace Vassallo Catheline N Vilain Julie Vogt Vanessa Wermenbol William P Whitehouse Doriette Soler Ivana Olivieri Simona Orcesi Mona S Aglan Maha S Zaki Ghada M H Abdel-Salam Adeline Vanderver Kai Kisand Flore Rozenberg Pierre Lebon Yanick J Crow

Lancet Neurol 2013 Dec 30;12(12):1159-69. Epub 2013 Oct 30.

Manchester Centre for Genomic Medicine, Institute of Human Development, Faculty of Medical and Human Sciences, University of Manchester, Manchester Academic Health Sciences Centre (MAHSC), Manchester, UK.

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December 2013

Genetic polymorphisms in NQO1 and SOD2: interactions with smoking, schistosoma infection, and bladder cancer risk in Egypt.

Authors:
David Goerlitz Sania Amr Chiranjeev Dash Doa'a A Saleh Mai El Daly Mohamed Abdel-Hamid Sherif El Kafrawy Tamer Hifnawy Sameera Ezzat Mohamed A Abdel-Aziz Hussein Khaled Yun-Ling Zheng Nabiel Mikhail Christopher A Loffredo

Urol Oncol 2014 Jan 10;32(1):47.e15-20. Epub 2013 Sep 10.

Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, DC. Electronic address:

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January 2014

Further delineation of the clinical spectrum in RNU4ATAC related microcephalic osteodysplastic primordial dwarfism type I.

Authors:
Ghada M H Abdel-Salam Mohamed S Abdel-Hamid Nihal A Hassan Mahmoud Y Issa Laila Effat Samira Ismail Mona S Aglan Maha S Zaki

Am J Med Genet A 2013 Aug 21;161A(8):1875-81. Epub 2013 Jun 21.

Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.

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August 2013

Frequent transient hepatitis C viremia without seroconversion among healthcare workers in Cairo, Egypt.

Authors:
Aline Munier Diaa Marzouk Florence Abravanel Mai El-Daly Sylvia Taylor Rasha Mamdouh Waleed Salah Eldin Hanan Ezz El-Arab Dalia Gaber Sos Mohamed Momen Omar Okasha Lenaig Le Fouler Mostafa El-Hosini Jacques Izopet Mona Rafik Matthew Albert Mohamed Abdel-Hamid Mostafa Kamal Mohamed Elisabeth Delarocque-Astagneau Arnaud Fontanet

PLoS One 2013 28;8(2):e57835. Epub 2013 Feb 28.

Emerging Diseases Epidemiology Unit, Institut Pasteur, Paris, France.

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August 2013

Genome-wide association study of spontaneous resolution of hepatitis C virus infection: data from multiple cohorts.

Authors:
Priya Duggal Chloe L Thio Genevieve L Wojcik James J Goedert Alessandra Mangia Rachel Latanich Arthur Y Kim Georg M Lauer Raymond T Chung Marion G Peters Gregory D Kirk Shruti H Mehta Andrea L Cox Salim I Khakoo Laurent Alric Matthew E Cramp Sharyne M Donfield Brian R Edlin Leslie H Tobler Michael P Busch Graeme Alexander Hugo R Rosen Xiaojiang Gao Mohamed Abdel-Hamid Richard Apps Mary Carrington David L Thomas

Ann Intern Med 2013 Feb;158(4):235-45

Johns Hopkins University School of Medicine, Baltimore, MD, USA.

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February 2013

Profound microcephaly, primordial dwarfism with developmental brain malformations: a new syndrome.

Authors:
Ghada M H Abdel-Salam Mohamed S Abdel-Hamid Sahar N Saleem Mahmoud K H Ahmed Mahmoud Issa Laila K Effat Hisham F Kayed Maha S Zaki Khaled R Gaber

Am J Med Genet A 2012 Aug 11;158A(8):1823-31. Epub 2012 Jul 11.

Division of Human Genetics and Genome Research, Department of Clinical Genetics, National Research Centre, Cairo, Egypt.

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August 2012

Analysis of IL28B variants in an Egyptian population defines the 20 kilobases minimal region involved in spontaneous clearance of hepatitis C virus.

Authors:
Vincent Pedergnana Mohamed Abdel-Hamid Julien Guergnon Amira Mohsen Lénaïg Le Fouler Ioannis Theodorou Mostafa Kamal Mohamed Arnaud Fontanet Sabine Plancoulaine Laurent Abel

PLoS One 2012 14;7(6):e38578. Epub 2012 Jun 14.

Laboratory of Human Genetics of Infectious Diseases, Necker Branch, Institut National de la Santé et de la Recherche Médicale U980, Paris, France.

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December 2012

Expanding the phenotypic and mutational spectrum in microcephalic osteodysplastic primordial dwarfism type I.

Authors:
Ghada M H Abdel-Salam Mohamed S Abdel-Hamid Mahmoud Issa Ahmed Magdy Ahmed El-Kotoury Khalda Amr

Am J Med Genet A 2012 Jun 11;158A(6):1455-61. Epub 2012 May 11.

Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.

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June 2012

Urinary bladder cancer risk factors in Egypt: a multicenter case-control study.

Authors:
Yun-Ling Zheng Sania Amr Doa'a A Saleh Chiranjeev Dash Sameera Ezzat Nabiel N Mikhail Iman Gouda Iman Loay Tamer Hifnawy Mohamed Abdel-Hamid Hussein Khaled Beverly Wolpert Mohamed A Abdel-Aziz Christopher A Loffredo

Cancer Epidemiol Biomarkers Prev 2012 Mar 6;21(3):537-46. Epub 2011 Dec 6.

Carcinogenesis, Biomarkers and Epidemiology Program, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, District of Columbia 20057, USA.

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March 2012

Risk factors for hepatitis C virus acquisition and predictors of persistence among Egyptian children.

Authors:
Gamal Esmat Mohamed Hashem Mona El-Raziky Wafaa El-Akel Suzan El-Naghy Nehal El-Koofy Rokaya El-Sayed Rasha Ahmed Mohamed Atta-Allah Mohamed Abdel Hamid Samer S El-Kamary Hanaa El-Karaksy

Liver Int 2012 Mar 15;32(3):449-56. Epub 2011 Sep 15.

Department of Tropical Medicine, Cairo University, Cairo, Egypt.

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March 2012

A homozygous mutation in RNU4ATAC as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder.

Authors:
Ghada M H Abdel-Salam Noriko Miyake Maha M Eid Mohamed S Abdel-Hamid Nihal A Hassan Ola M Eid Laila K Effat Tarek H El-Badry Ghada Y El-Kamah Mohamed El-Darouti Naomichi Matsumoto

Am J Med Genet A 2011 Nov 11;155A(11):2885-96. Epub 2011 Oct 11.

Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.

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November 2011

Genetic polymorphism in IL28B is associated with spontaneous clearance of hepatitis C virus genotype 4 infection in an Egyptian cohort.

Authors:
Fuat Kurbanov Mohamed Abdel-Hamid Rachel Latanich Jacquie Astemborski Mostafa Mohamed Nabiel Mh Mikhail Mai El-Daly Sherif El-Kafrawy David L Thomas Chloe L Thio

J Infect Dis 2011 Nov 20;204(9):1391-4. Epub 2011 Sep 20.

Department of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.

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November 2011

The Core/E1 domain of hepatitis C virus genotype 4a in Egypt does not contain viral mutations or strains specific for hepatocellular carcinoma.

Authors:
Xiaoan Zhang Soo Hyung Ryu Yanjuan Xu Tamerl Elbaz Abdel-Rahman N Zekri Ashraf Omar Abdelaziz Mohamed Abdel-Hamid Valerie Thiers Santiago F Elena Xiaofeng Fan Adrian M Di Bisceglie

J Clin Virol 2011 Dec 17;52(4):333-8. Epub 2011 Sep 17.

Division of Gastroenterology and Hepatology, Department of Internal Medicine, Saint Louis University School of Medicine, St. Louis, MO 63104, USA.

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December 2011

Association of HCV with diabetes mellitus: an Egyptian case-control study.

Authors:
Eman I Elhawary Gamal F Mahmoud Mai A El-Daly Fatma A Mekky Gamal G Esmat Mohamed Abdel-Hamid

Virol J 2011 Jul 26;8:367. Epub 2011 Jul 26.

Microbiology Department, Faculty of Pharmacy, Minia University, Minia, Egypt.

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July 2011

GSTM1, GSTT1 null variants, and GPX1 single nucleotide polymorphism are not associated with bladder cancer risk in Egypt.

Authors:
David Goerlitz Mai El Daly Mohamed Abdel-Hamid Doa'a A Saleh Lenka Goldman Sherif El Kafrawy Tamer Hifnawy Sameera Ezzat Mohamed A Abdel-Aziz Mohamed Saad Zaghloul Saber Rafat Ali Hussein Khaled Sania Amr Yun-Ling Zheng Nabiel Mikhail Christopher Loffredo

Cancer Epidemiol Biomarkers Prev 2011 Jul 17;20(7):1552-4. Epub 2011 May 17.

Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, DC 20007, USA.

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July 2011

Associations differ by sex for catechol-O-methyltransferase genotypes and bladder cancer risk in South Egypt.

Authors:
Beverly J Wolpert Sania Amr Doa'a A Saleh Sameera Ezzat Iman Gouda Iman Loay Tamer Hifnawy Mohamed Abdel-Hamid Nabiel N Mikhail Min Zhan Yun-Ling Zheng Katherine Squibb Mohamed A Abdel-Aziz Mohamed S Zaghloul Hussein Khaled Christopher A Loffredo

Urol Oncol 2012 Nov-Dec;30(6):841-7. Epub 2011 Mar 11.

Department of Epidemiology and Public Health, University of Maryland School of Medicine, Baltimore, MD 21201, USA.

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July 2013

Waterpipe Smoking And The DRD2/ANKK1 Genotype.

Authors:
Ghada N Radwan Christopher A Loffredo Maged A El Setouhy Mohamed Abdel Hamid Ebenezer J Israel Mostafa K Mohamed

J Egypt Public Health Assoc 2010 ;85(3-4):131-48

Dept. of Public Health, Cairo University, Cairo, Egypt.

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November 2015

Would coronary collaterals to the infarct-related artery serve as a marker of viability in patients with prior myocardial infarction? A study with trimetazidine-(99m)Tc-sestamibi imaging.

Authors:
Amr Adel Abdel-Hamid Mohamed Wail Nammas

Cardiovasc Revasc Med 2011 Jan-Feb;12(1):41-6. Epub 2010 Oct 20.

Faculty of Medicine, Cardiology Department, Ain Shams University, Cairo, Egypt.

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May 2011

Estrogen exposure and bladder cancer risk in Egyptian women.

Authors:
Beverly J Wolpert Sania Amr Sameera Ezzat Doa'a Saleh Iman Gouda Iman Loay Tamer Hifnawy Nabiel N Mikhail Mohamed Abdel-Hamid Min Zhan Yun-Ling Zheng Katherine Squibb Mohamed A Abdel-Aziz Mohamed Zaghloul Hussein Khaled Christopher A Loffredo

Maturitas 2010 Dec 1;67(4):353-7. Epub 2010 Sep 1.

Department of Epidemiology and Preventive Medicine, University of Maryland School of Medicine, Baltimore, MD 21201, USA.

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December 2010

Opening-wedge high tibial osteotomy without bone graft.

Authors:
Maher A El-Assal Yaser E Khalifa Mohamed M Abdel-Hamid Hatem G Said Hatem M A Bakr

Knee Surg Sports Traumatol Arthrosc 2010 Jul 27;18(7):961-6. Epub 2010 Mar 27.

Department of Orthopaedics, Assiut University Hospital, 71526 Assiut, Egypt.

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July 2010

Combined percutaneous endovascular iliac angioplasty and infrainguinal surgical revascularization for chronic lower extremity ischemia: preliminary result.

Authors:
Ahmed Mousa Mohamed Abdel-Hamid Ashraf Ewida Mohamed Saad Alaa Sahrabi

Vascular 2010 Mar-Apr;18(2):71-6

Division of Vasular & Endocasular Surgery, Faculty of Medicine, Al-Azhar University, Vario, Egypt.

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June 2010

Incidence and risk factors for community-acquired hepatitis C infection from birth to 5 years of age in rural Egyptian children.

Authors:
Doa'a A Saleh Fatma M Shebl Samer S El-Kamary Laurence S Magder Alif Allam Mohamed Abdel-Hamid Nabiel Mikhail Mohamed Hashem Soraya Sharaf Sonia K Stoszek G Thomas Strickland

Trans R Soc Trop Med Hyg 2010 May 12;104(5):357-63. Epub 2010 Feb 12.

Department of Community Medicine, Faculty of Medicine, Cairo University, Cairo, Egypt.

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May 2010

Is the hepatitis C virus epidemic over in Egypt? Incidence and risk factors of new hepatitis C virus infections.

Authors:
Aya Mostafa Sylvia M Taylor Mai el-Daly Mostafa el-Hoseiny Iman Bakr Naglaa Arafa Valérie Thiers François Rimlinger Mohamed Abdel-Hamid Arnaud Fontanet Mostafa K Mohamed

Liver Int 2010 Apr 5;30(4):560-6. Epub 2010 Feb 5.

Department of Community, Environmental and Occupational Medicine, Faculty of Medicine, Ain Shams University, Cairo, Egypt.

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April 2010