Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Azza Tantawy"'
Publikováno v:
Journal of Taibah University Medical Sciences, Vol 18, Iss 6, Pp S17-S18 (2023)
Externí odkaz:
https://doaj.org/article/f38cd9279e954293849a2c7ad5c58be4
Wolman disease in patients with familial hemophagocytic lymphohistiocytosis (FHL) negative mutations
Autor:
Solaf Elsayed, Ezzat Elsobky, Azza Tantawy, Eman Ragab, Marine Gil, Nathalie Lambert, Geneviève de Saint Basile
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 17, Iss 3, Pp 277-280 (2016)
Background: Familial hemophagocytic lymphohistiocytosis is a rare autosomal recessive disease that is usually evident in the first few months or years of life. Major signs and symptoms include hepatomegaly, splenomegaly, anemia, leucopenia or thrombo
Externí odkaz:
https://doaj.org/article/414547d6dac24ecfaaf7d421811494f5
Autor:
Azza Tantawy, Nayera El-Sherif, Sara Makkeyah, Nahed Salah Eldeen, Noura Bahaa El-Din Farghal, Nanies Soliman, Fatma S. E. Ebeid
Publikováno v:
Annals of Hematology. 102:271-281
Sleep disordered breathing (SDB) is a common underdiagnosed sequela of sickle cell disease (SCD) that has been linked to the frequency of vaso-occlusive crises. To determine the frequency of SDB in children with SCD and its association to SCD-related