Sherif F Abdel-Ghafar - Div Human Genet & Genome Res, Natl Res Ctr

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论文共 20 篇作者统计合作学者相似作者

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Delineating the Clinical and Brain Imaging Characteristics of the Neonatal Form of CSTB-Related Neurodevelopmental Disorders

Mohamed S Abdel-Hamid,Sherif F Abdel-Ghafar,Inas S M Sayed,Maha S Zaki, Ghada M H Abdel-Salam

Clinical genetics (2025)

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Deciphering the Phenotypic Spectrum Associated with MIA3-related Odontochondrodysplasia

Mohamed S Abdel-Hamid, Rasha M Elhossini,Sherif F Abdel-Ghafar, Mennat Mehrez, Mona S Aglan,Nehal F Hassib

Journal of human geneticsno. 5 (2025): 257-263

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Novel Homozygous ESAM Variants in Two Families with Perinatal Strokes Showing Variable Neuroradiologic and Clinical Findings

Ghada M. H. Abdel-Salam, Asmaa Esmail, Dina Nagy,Sherif F. Abdel-Ghafar,Mohamed S. Abdel-Hamid

Journal of Human Genetics（2024）

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Refining the Phenotypic Spectrum of CCDC88A-related PEHO-like Syndrome

Mahmoud Y. Issa,Mona A. Hafez,Samir M. Mounir,Sherif F. Abdel Ghafar,Maha S. Zaki,Mohamed S. Abdel-Hamid

AMERICAN JOURNAL OF MEDICAL GENETICS PART Ano. 2 (2024): 226-232

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The Clinical and Genetic Landscape of Developmental and Epileptic Encephalopathies in Egyptian Children

Nour Elkhateeb,Mahmoud Y. Issa,Hasnaa M. Elbendary,Walaa Elnaggar,Areef Ramadan,Karima Rafat,Mona Kamel,Sherif F. Abdel-Ghafar,Fawzia Amer, Hebatallah M. Hassaan,Roberta Trunzo,Catarina Pereira,Mohamed S. Abdel-Hamid,Felice D'Arco,Peter Bauer,Aida M. Bertoli-Avella,Marian Girgis,Joseph G. Gleeson,Maha S. Zaki,Laila Selim

CLINICAL GENETICSno. 5 (2024): 510-522

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A Missense Variant in EXOSC8 Causes Exon Skipping and Expands the Phenotypic Spectrum of Pontocerebellar Hypoplasia Type 1C

Maha S. Zaki,Sherif F. Abdel-Ghafar,Mohamed S. Abdel-Hamid

Journal of Human Genetics（2024）

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Delineating the Phenotype of PNPLA8-related Mitochondriopathies

Mohamed S. Abdel-Hamid,Ghada M. H. Abdel-Salam,Sherif F. Abdel-Ghafar,Maha S. Zaki

CLINICAL GENETICS（2024）

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Ghada A. Otaify,Rasha M. Elhossini,Sherif F. Abdel-Ghafar,Inas M. Sayed,Ghada M. H. Abdel-Salam,Mona S. Aglan,Mohamed S. Abdel-Hamid

AMERICAN JOURNAL OF MEDICAL GENETICS PART Ano. 8 (2023): 2100-2112

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An Atypical Expression of Core Α-Dystroglycan and Laminin-α2 in Skin Fibroblasts of Patients with Congenital Muscular Dystrophies

Sahar Sabry,Mahmoud Y Issa,Mohamed S Abdel-Hamid,Noura R Eissa,Sherif F Abdel-Ghafar,Mona M Ibrahim,Maha S Zaki

MOLECULAR BIOLOGY REPORTSno. 8 (2023): 6373-6379

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Congenital Leptin and Leptin Receptor Deficiencies in Nine New Families: Identification of Six Novel Variants and Review of Literature

Inas H. Mazen,Mona A. El-Gammal,Aya A. Elaidy,Ghada M. Anwar,Engy A. Ashaat,Sherif F. Abdel-Ghafar,Mohamed S. Abdel-Hamid

Molecular Genetics and Genomics（2023）

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