Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Maha Al Awadi"'
Autor:
Nouh Al-Mahrouqi, Maha Al Awadi, Aisha Al Hosni, Murtadha Al Khabori, Abdul Hakim Al Rawas, Mohammed Al Rawahi, Ameera Al-Rahbi, Shahina Daar, Yasser Wali
Publikováno v:
HemaSphere, Vol 7, p e14677e9 (2023)
Externí odkaz:
https://doaj.org/article/2acb9410d8e142daa24bf1f31b2f6876
Autor:
John N. Brewin, Maha Al Awadi, Taimoora Al‐Subhi, Anke Hannemann, Halima Al Balushi, John S. Gibson, Yasser Wali, David C. Rees
Publikováno v:
British Journal of Haematology. 179:256-265
Studying different sickle cell genotypes may throw light on the pathogenesis of sickle cell disease (SCD). Here, the clinical profile, red cell sickling and K+ permeability in 29 SCD patients (15 patients with severe disease and 14 with a milder form
Autor:
Halima W M, Al Balushi, Yasser, Wali, Maha, Al Awadi, Taimoora, Al-Subhi, David C, Rees, John N, Brewin, Anke, Hannemann, John S, Gibson
Publikováno v:
British journal of haematology. 179(2)
Studying different sickle cell genotypes may throw light on the pathogenesis of sickle cell disease (SCD). Here, the clinical profile, red cell sickling and K
Publikováno v:
Medical Principles and Practice
Objective: To determine the molecular basis of familial ichthyosis in three Omani families. Subjects and Methods: Nine patients from three consanguineous families, A, B, and C, were born with typical features of lamellar ichthyosis subtype including
Autor:
Birgit Leitinger, Adila Al-Kindi, Anuradha Ganesh, Huifang Xu, Bassam R. Ali, Abeer Al Sayegh, Lihadh Al-Gazali, Praseetha Kizhakkedath, Anne John, Maha Al-Awadi, Lamya Al-Anbouri
Publikováno v:
BMC Medical Genetics
Background The rare autosomal genetic disorder, Spondylo-meta-epiphyseal dysplasia with short limbs and abnormal calcifications (SMED-SL), is reported to be caused by missense or splice site mutations in the human discoidin domain receptor 2 (DDR2) g