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.

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.

View Article and Find Full Text PDF
December 2020

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

Neuropediatrics 2020 Dec 3. Epub 2020 Dec 3.

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

View Article and Find Full Text PDF
December 2020

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

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.

View Article and Find Full Text PDF
November 2020

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

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:

View Article and Find Full Text PDF
November 2020

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

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.

View Article and Find Full Text PDF
December 2020

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

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

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

View Article and Find Full Text PDF
November 2020

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

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.

View Article and Find Full Text PDF
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.

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.

View Article and Find Full Text PDF
August 2020

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

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.

View Article and Find Full Text PDF
May 2020

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

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.

View Article and Find Full Text PDF
August 2020

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

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.

View Article and Find Full Text PDF
July 2020

KBG syndrome in two patients from Egypt.

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.

View Article and Find Full Text PDF
June 2020

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

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

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

View Article and Find Full Text PDF
January 2020

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

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.

View Article and Find Full Text PDF
January 2020

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

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

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

View Article and Find Full Text PDF
March 2020

Lenz-Majewski syndrome in a patient from Egypt.

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.

View Article and Find Full Text PDF
October 2019

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

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

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

View Article and Find Full Text PDF
September 2019

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

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.

View Article and Find Full Text PDF
March 2019

Phenotypic and molecular insights into PQBP1-related intellectual disability.

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.

View Article and Find Full Text PDF
November 2018

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

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.

View Article and Find Full Text PDF
May 2019

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

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.

View Article and Find Full Text PDF
October 2018

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

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.

View Article and Find Full Text PDF
April 2018

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

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.

View Article and Find Full Text PDF
June 2017

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

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.

View Article and Find Full Text PDF
January 2018

Aicardi-Goutières syndrome: unusual neuro-radiological manifestations.

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.

View Article and Find Full Text PDF
June 2017

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

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.

View Article and Find Full Text PDF
April 2017

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

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.

View Article and Find Full Text PDF
April 2017

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

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.

View Article and Find Full Text PDF
April 2017

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

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.

View Article and Find Full Text PDF
November 2017

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

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:

View Article and Find Full Text PDF
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.

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:

View Article and Find Full Text PDF
January 2017

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

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.

View Article and Find Full Text PDF
September 2016

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

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.

View Article and Find Full Text PDF
October 2016

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

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.

View Article and Find Full Text PDF
September 2016

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

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.

View Article and Find Full Text PDF
August 2016

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

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.

View Article and Find Full Text PDF
July 2016

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

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:

View Article and Find Full Text PDF
June 2016

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

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

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

View Article and Find Full Text PDF
January 2017

Occult hepatitis C virus infection among Egyptian hemodialysis patients.

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.

View Article and Find Full Text PDF
August 2016

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

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.

View Article and Find Full Text PDF
November 2015

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

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

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

View Article and Find Full Text PDF
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.

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.

View Article and Find Full Text PDF
January 2016

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

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

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

View Article and Find Full Text PDF
March 2016

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

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.

View Article and Find Full Text PDF
March 2016

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

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.

View Article and Find Full Text PDF
May 2015

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

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.

View Article and Find Full Text PDF
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.

View Article and Find Full Text PDF
February 2015

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

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.

View Article and Find Full Text PDF
September 2014

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

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.

View Article and Find Full Text PDF
November 2014

APOA2 Polymorphism in Relation to Obesity and Lipid Metabolism.

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.

View Article and Find Full Text PDF
January 2014

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

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.

View Article and Find Full Text PDF
February 2015

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

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.

View Article and Find Full Text PDF
August 2013

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

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.

View Article and Find Full Text PDF
August 2012

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

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.

View Article and Find Full Text PDF
June 2012

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

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.

View Article and Find Full Text PDF
March 2012

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

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.

View Article and Find Full Text PDF
December 2011

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

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

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

View Article and Find Full Text PDF
July 2011

Waterpipe Smoking And The DRD2/ANKK1 Genotype.

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

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

View Article and Find Full Text PDF
November 2015

Opening-wedge high tibial osteotomy without bone graft.

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.

View Article and Find Full Text PDF
July 2010

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

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.

View Article and Find Full Text PDF
April 2010