Publications by authors named "Walid Fawzy"

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Familial Glucocorticoid Deficiency Type 4 Caused by a Novel Mutation in the Nicotinamide Nucleotide Transhydrogenase (NNT) Gene: A Clinical Report of Two Siblings.
Ali S Alquraishi, Ahmed Albishri, Badriah G Alasmari, Walid Fawzy, Ali Hawan

Cureus· January 2025

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Spinal Muscular Atrophy with Respiratory Distress
Type 1: A Novel Variant of IGHMBP2 Gene.
Muhammad Saeed, Walid Fawzy, Saeed Al-Tala, Tayseer Adel Magid, Hala Ahmed

J Coll Physicians Surg Pak· December 2021

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