Results 141 to 150 of about 3,107 (209)

Molecular Pathogenesis of Inherited Platelet Dysfunction. [PDF]

Biomolecules
Rodríguez-Alén A, Moscardó A, Bastida JM, Rivera J.   +3 more
europepmc   +1 more source

The co-inheritance of two <i>ITGB3</i> variants with additive detrimental effects on platelets leads to variant Glanzmann thrombasthenia. [PDF]

Haematologica
Arndt N, Falcinelli E, Zamora-Canovas A, Fuentes AS, Marin-Quilez A, Nieto-Hernandez MDM, Rivera J, Gresele P, Bury L.   +8 more
europepmc   +1 more source

Glanzmann Thrombasthenia in a Newborn Due to a Rare Homozygous Missense Mutation. [PDF]

Cureus
Faraz S, Nikhat F, Hayel Suleiman Beshtawi H, Malik SA, Yahya Hashim K.   +4 more
europepmc   +1 more source

Novel homozygous frameshift mutation of ITGB3 in the Glanzmann thrombasthenia patient with abnormal bone metabolism and congenital bone defects. [PDF]

Orphanet J Rare Dis
Luo Y, Guo N, Wang Y, Li J.
europepmc   +1 more source

Concomitant Systemic Lupus Erythematosus and Glanzmann Thrombocytopenia: A Case Report and Literature Review. [PDF]

Case Rep Rheumatol
Noory M, Hajian H, Kompani F, Kiumarsi A, Shahrooei M, Ziaee V.   +5 more
europepmc   +1 more source

Thrombopathic thrombasthenia.

The Indian journal of medical research, 1982
A K, Saraya, P, Kapoor, J, Kasturi
openaire   +1 more source

Gastrointestinal Bleeding/Angiodysplasia in Patients With Glanzmann Thrombasthenia. [PDF]

J Med Cases
Tarawah RA, Tarawah AM.
europepmc   +1 more source

Epidemiological and clinical characteristics of children and young adults with Glanzmann's thrombasthenia in upper Egypt: a multicenter cross-sectional study. [PDF]

Ann Hematol
Khalifa GLAH, El-Sayed AA, Elmasry Z, Elsayh KI, Atwa ZT, Morgan DS, Hassan EE, Hassan MA, Youssef MAM.   +8 more
europepmc   +1 more source

[Thrombasthenia and pseudohemophilia].

Boletin medico del Hospital Infantil de Mexico, 1998
A H, TORO, J, ARIAS Y ARIAS, S, DORANTES MESA, R, SOTO ALLANDE, I, BARRON FLORES   +4 more
openaire   +1 more source