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Y Girgis

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American Journal of Medical Genetics. Part A|October 14, 2024

Clinical and Genetic Spectrum of Patients With Mitochondrial Disease in a Pediatric Egyptian Cohort: Novel Variants and Phenotypic ExpansionHebatallah M Hassaan, Angela Pyle, Nihal Almenabawy, et al.

Journal of Medical Screening|January 22, 2016

Inborn errors of metabolism detectable by tandem mass spectrometry in Egypt: The first newborn screening pilot studyFayza A Hassan, Fatma El-Mougy, Sahar A Sharaf, et al.

Journal of Neurology, Neurosurgery, and Psychiatry|October 9, 2013

PRRT2 mutations: exploring the phenotypical boundariesTania Djémié, Sarah Weckhuysen, Philip Holmgren, et al.

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Search research articles

Showing results (21-30 of 23) with videos related to

Sort By:

Pageof 3

You have reached the last page of results.This site can display upto 23 results.

American Journal of Medical Genetics. Part A|October 14, 2024

Clinical and Genetic Spectrum of Patients With Mitochondrial Disease in a Pediatric Egyptian Cohort: Novel Variants and Phenotypic ExpansionHebatallah M Hassaan, Angela Pyle, Nihal Almenabawy, et al.

Journal of Medical Screening|January 22, 2016

Inborn errors of metabolism detectable by tandem mass spectrometry in Egypt: The first newborn screening pilot studyFayza A Hassan, Fatma El-Mougy, Sahar A Sharaf, et al.

Journal of Neurology, Neurosurgery, and Psychiatry|October 9, 2013

PRRT2 mutations: exploring the phenotypical boundariesTania Djémié, Sarah Weckhuysen, Philip Holmgren, et al.

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