Cholestasis in patients with Cockayne syndrome and suggested modified criteria for clinical diagnosis

por Abdel Ghaffar, Tawhida Y, Elsobky, Ezzat S, Elsayed, Solaf M
Publicado 2011

Phenotypic and Genetic Characterization of a Cohort of Pediatric Wilson Disease Patients

por Abdel Ghaffar, Tawhida Y, Elsayed, Solaf M, Elnaghy, Suzan, Shadeed, Ahmed, Elsobky, Ezzat S, Schmidt, Hartmut
Publicado 2011

A novel ABHD5 mutation in two Chanarin Dorfman siblings with severe and heterogeneous clinical phenotype

por Elsayed, Solaf Mohamed, Torre, Enza, Tavian, Daniela, Moro, Laura, Angelini, Corrado, Abdel Ghaffar, Tawhida Y., Zalata, Khalid, Fahmy, Enas Ezzeldein, Missaglia, Sara
Publicado 2022

Clinical Benefits of Biochemical Markers of Fibrosis in Egyptian Children With Chronic Liver Diseases

por Abdel-Ghaffar, Tawhida Y., Behairy, Behairy E., El-Shaheed, Azza Abd, Mahdy, Karam, El-Batanony, Mohamed, Hussein, Mohsen H., Sira, Mostafa M.
Publicado 2010

MPI‐CDG from a hepatic perspective: Report of two Egyptian cases and review of literature

por Abdel Ghaffar, Tawhida Y., Ng, Bobby G., Elsayed, Solaf M., El Naghi, Suzan, Helmy, Sarah, Mohammed, Nermine, El Hennawy, Ahmed, Freeze, Hudson H.
Publicado 2020