Results 81 to 90 of about 1,325 (125)

Dual hemostatic defects in Glanzmann thrombasthenia and von Willebrand disease: functional characterization of ITGA2B and dominant-negative von Willebrand factor variants. [PDF]

open access: yesRes Pract Thromb Haemost
Zhang Y   +14 more
europepmc   +1 more source

Monozygotic twin cases of endometriosis with Glanzmann thrombasthenia: a case report and review of literature. [PDF]

open access: yesOrphanet J Rare Dis, 2023
Rokhgireh S   +6 more
europepmc   +1 more source

Management of pregnancy and childbirth in Glanzmann thrombasthenia: A case series and review. [PDF]

open access: yesBr J Haematol
Rutten KHG   +9 more
europepmc   +1 more source

A single F153Sβ3 mutation causes constitutive integrin αIIbβ3 activation in a variant form of Glanzmann thrombasthenia. [PDF]

open access: yesBlood Adv, 2023
Koukouritaki SB   +12 more
europepmc   +1 more source

Emergency management of patients with Glanzmann thrombasthenia: consensus recommendations from the French reference center for inherited platelet disorders. [PDF]

open access: yesOrphanet J Rare Dis, 2023
Fiore M   +19 more
europepmc   +1 more source

Natural history & quality of life in Glanzmann thrombasthenia & Bernard Soulier syndrome: An observational study from India. [PDF]

open access: yesIndian J Med Res
Kharat SV   +8 more
europepmc   +1 more source

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