Publications by authors named "Marian Girgis"

16Publications

Disparities in the Uptake of Telemedicine During the COVID-19 Surge in a Multidisciplinary Head and Neck Cancer Population by Patient Demographic Characteristics and Socioeconomic Status.

JAMA Otolaryngol Head Neck Surg 2020 Nov 5. Epub 2020 Nov 5.

Department of Otolaryngology-Head and Neck Surgery, Henry Ford Health System and Henry Ford Cancer Institute, Detroit, Michigan.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1001/jamaoto.2020.3052DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7645752PMC
November 2020

Cold agglutinin disease and autoimmune hemolytic anemia with pulmonary embolism as a presentation of COVID-19 infection.

Hematol Oncol Stem Cell Ther 2020 Jul 6. Epub 2020 Jul 6.

Division of Hematology and Oncology, Department of Internal Medicine, Henry Ford Health System, Wayne State University, Detroit, MI, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.hemonc.2020.06.005DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7336954PMC
July 2020

Further Insights into Developmental Brain Malformations and Leukoencephalopathy Associated with 6p25.3 Deletion.

Neuropediatrics 2020 02 21;51(1):76-82. Epub 2019 Oct 21.

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

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1055/s-0039-1698421DOI Listing
February 2020

Implementation of ketogenic diet in children with drug-resistant epilepsy in a medium resources setting: Egyptian experience.

Epilepsy Behav Case Rep 2019 23;11:35-38. Epub 2018 Nov 23.

Department of Pediatrics, Clinical Nutrition Division, Cairo University Hospital, Cairo, Egypt.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ebcr.2018.11.001DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6312833PMC
November 2018

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

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.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.61021DOI Listing
February 2019

Polymorphisms of Immunoglobulin G Fc Receptors in Pediatric Guillain-Barré Syndrome.

Neuropediatrics 2016 Jun 11;47(3):151-6. Epub 2016 Apr 11.

Department of Clinical Pathology, Faculty of Medicine, Cairo University, Cairo, Egypt.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1055/s-0036-1579633DOI Listing
June 2016

Lysosomal Storage Disorders in Egyptian Children.

Indian J Pediatr 2016 Aug 2;83(8):805-13. Epub 2016 Feb 2.

Inherited Metabolic Disease Unit (IMDU), Cairo University Children's Hospital, Cairo, Egypt.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s12098-015-2014-xDOI Listing
August 2016

Inborn errors of metabolism detectable by tandem mass spectrometry in Egypt: The first newborn screening pilot study.

J Med Screen 2016 09 20;23(3):124-9. Epub 2016 Jan 20.

Clinical and Chemical Pathology Department, Faculty of Medicine, Cairo University, Cairo, Egypt Inherited Metabolic Disease Unit, Center of Social and Preventive Medicine, Cairo University, Cairo, Egypt

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1177/0969141315618229DOI Listing
September 2016

Skeletal and cardiac muscle involvement in children with glycogen storage disease type III.

Eur J Pediatr 2015 Nov 7;174(11):1545-8. Epub 2015 May 7.

Department of Pediatrics, Kasr Alainy Medical School, Cairo University, Cairo, Egypt.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00431-015-2546-0DOI Listing
November 2015

Association of genetic polymorphism of pre-microRNA-146a rs2910164 and serum high-mobility group box 1 with febrile seizures in Egyptian children.

J Child Neurol 2015 Mar 15;30(4):437-44. Epub 2014 Oct 15.

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

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1177/0883073814550312DOI Listing
March 2015

Selective screening for inborn errors of metabolism by tandem mass spectrometry in Egyptian children: a 5 year report.

Clin Biochem 2014 Jun 13;47(9):823-8. Epub 2014 Apr 13.

Inherited Metabolic Disease Unit, Cairo University Children Hospital, Cairo, Egypt; Department of Clinical and Chemical Pathology, Faculty of Medicine, Cairo University, Egypt.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.clinbiochem.2014.04.002DOI Listing
June 2014

Clinical, neuroimaging, and genetic characteristics of megalencephalic leukoencephalopathy with subcortical cysts in Egyptian patients.

Pediatr Neurol 2014 Feb 24;50(2):140-8. Epub 2013 Oct 24.

Stem Cell Research Laboratory, Centre for Advanced Sciences-National Research Centre, Cairo, Egypt; Neurogenetics Laboratory, Weill Cornell Medical College in Qatar, Doha, Qatar; Department of Neurology, Weill Cornell Medical College, New York, New York. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.pediatrneurol.2013.10.008DOI Listing
February 2014