Search Results - "Aldor, Shahad M"

A point mutation in Phe71Ser in glycoprotein IX as a genetic cause of Bernard–Soulier syndrome: case report by Alsahafi, Imtinan K., Al‐Harbi, Ibrahim, Aldor, Shahad M., Albarakati, Bilqis A., Alahmadi, Ghaida B.

“…Key Clinical Message We need to be aware of rare causes of persistent thrombocytopenia as Bernard–Soulier syndrome (BSS). When BSS is suspected based on family…”
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A point mutation in Phe71Ser in glycoprotein IX as a genetic cause of Bernard-Soulier syndrome: case report by Alsahafi, Imtinan K, Al-Harbi, Ibrahim, Aldor, Shahad M, Albarakati, Bilqis A, Alahmadi, Ghaida B

“…We need to be aware of rare causes of persistent thrombocytopenia as Bernard-Soulier syndrome (BSS). When BSS is suspected based on family history and giant…”
Get full text