Results 91 to 100 of about 1,427 (120)

High prevalence of the natural Asn89Asp mutation in the GP1BB gene associated with Bernard-Soulier syndrome in French patients from the genetic isolate of Reunion Island. [PDF]

Br J Haematol, 2020
Fiore M, De Thoré C, Randrianaivo-Ranjatoelina H, Baas MJ, Jacquemont ML, Dreyfus M, Lavenu-Bombled C, Li R, Gachet C, Dupuis A, Lanza F.   +10 more
europepmc   +1 more source

Bernard Soulier Syndrome: 10 years' experience at a tertiary care hospital. [PDF]

Pak J Med Sci, 2019
Farhan S, Iqbal I, Ahmed N.
europepmc   +1 more source

Management of haemostasis during dental extraction in a Bernard-Soulier syndrome child. [PDF]

BMJ Case Rep, 2019
Sharma S, Chak RK, Khanna R.
europepmc   +1 more source

Combined occurrence of Bernard-Soulier syndrome and prekallikrein deficiency. [PDF]

Blood Res, 2017
Shahverdi E, Abolghasemi H, Ahmadinejad M.   +2 more
europepmc   +1 more source

WCN25-1779 SUCCESSFUL KIDNEY REPLACEMENT THERAPY IN BERNARD SOULIER SYNDROME ; CHALLENGES FOR NEPHROLOGIST

Kidney International Reports
Aniket Hase, Niwrutti Hase, Dipanjan Haldar, Ankita Hingolikar, Asif Shaikh, Radhika Agarwal, Pratik Hatkar   +6 more
doaj   +1 more source

A Brazilian case of Bernard-Soulier syndrome with two distinct founder mutations. [PDF]

Hum Genome Var, 2017
Kanda K, Kunishima S, Sato A, Abe D, Nishijima S, Ishigami T.   +5 more
europepmc   +1 more source

A point mutation in Phe71Ser in glycoprotein IX as a genetic cause of Bernard-Soulier syndrome: case report. [PDF]

Clin Case Rep, 2018
Alsahafi IK, Al-Harbi I, Aldor SM, Albarakati BA, Alahmadi GB.   +4 more
europepmc   +1 more source

Primigravida with Bernard-Soulier Syndrome: a case report. [PDF]

BMC Res Notes, 2015
Macêdo MB, Brito Jde M, Macêdo Pda S, Brito JA.   +3 more
europepmc   +1 more source