Alice AbdelAleem

3PUBLICATIONS
0CO-AUTHORS
Major global burdens of diseaseNeonatologyNeurology and neuromuscular diseases
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Publications (3)

|Mar 13, 2023
Biochemical and mutational analyses of HEXA in a cohort of Egyptian patients with infantile Tay-Sachs disease. Expansion of the mutation spectrum.

Doaa M A Ibrahim, Ola S M Ali, Hala Nasr

|Feb 13, 2023
Cohen syndrome and early-onset epileptic encephalopathy in male triplets: two disease-causing mutations in VPS13B and NAPB.

Alice AbdelAleem, Naim Haddad, Ghada Al-Ettribi

|Aug 09, 2017
Homozygous nonsense mutation in SCHIP1/IQCJ-SCHIP1 causes a neurodevelopmental brain malformation syndrome.

M F Elsaid, N Chalhoub, T Ben-Omran

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