Results 91 to 100 of about 2,361,484 (180)

ePoster

European Journal of Neurology, Volume 33, Issue S1, June 2026.
wiley   +1 more source

Autobiographie de Monsieur Pierre Soulier, conversation

, 1946
Description analytique : Autobiographie de Monsieur Pierre Soulier ...
Musée national des arts et traditions populaires (Paris), Centre d'ethnologie française   +1 more
core   +2 more sources

Treatment of recurrent gastrointestinal bleeding with recombinant factor VIIa in a patient with Bernard-Soulier syndrome

, 2005
The Bernard-Soulier syndrome (BSS) is a rare disorder of platelet function which is characterized by a prolonged bleeding time, giant platelets, and thrombocytopenia. Treatment of hemorrhage in patients with BSS usually requires platelet transfusion, but
Ovalı, Ercüment, EREN, NECMİ, Karti, SS, ÖZGÜR, ORHAN, Kartı, sami, Yilmaz, M, Eren, N, Yilmaz, Mustafa, Ovali, E, Ozgur, O   +9 more
core   +1 more source

Lentiviral gene therapy reverts GPIX expression and phenotype in Bernard-Soulier syndrome type C. [PDF]

Mol Ther Nucleic Acids, 2023
De Cristofaro R.
europepmc   +2 more sources

FREQUENCY OF INHERITED PLATELE FUNCTION DISORDERS–ARMED FORCES INSTITUTE OF PATHOLOGY EXPERIENCE

Pakistan Armed Forces Medical Journal, 2020
Objective: To determine the frequency and clinical features of inherited platelet function disorders diagnosed at Armed Forces Institute of Pathology. Study Design: Cross sectional study.
Saira Irum, Helen Mary Robert, Asad Mahmood, Rafia Mahmood, Ayesha Khurshid, Mansoor Ishaq   +5 more
doaj  

Flow cytometry immunophenotyping of healthy platelets and hospitalized patients with suspected platelet dysfunction: Challenges for establishing a cutoff value

Hematology, Transfusion and Cell Therapy
Introduction and Objective: Flow Cytometry (FC) is one of the techniques, which allows the identification and characterization of platelets. The detection of absent or reduced expression of the glycoproteins is the main objective of this technique ...
Daiane Keller Cecconello, Fabiane Spagnol, Ana Paula Alegretti, Diogo André Pilger, Mariela Granero Farias   +4 more
doaj   +1 more source

A novel germline mutation in GP1BA gene N-terminal domain in monoallelic Bernard-Soulier syndrome

, 2018
Mutations in the GP1BA gene have been associated with platelet-type von Willebrand disease and Bernard-Soulier syndrome. Here, we report a novel GP1BA mutation in a family with autosomal dominant macrothrombocytopenia and mild bleeding.
Olga Stehlíková (5867498), Lenka Radová (4326136), Milan Pacejka (5867504), Šárka Pospíšilová (522791), Jakub Trizuljak (5867486), Kamila Réblová (415711), Jiřina Zavřelová (5867501), Michael Doubek (471232), Petr Smejkal (3860542), Karol Pál (5867495), Michaela Pešová (5867492), Jiří Mayer (5867507), Kateřina Staňo Kozubík (5867489)   +12 more
core   +1 more source

Bernard-Soulier syndrome [PDF]

, 2020
openaire   +3 more sources

Molecular genetic analysis of patients with Bernard Soulier syndrome, Hermansky Pudlak syndrome and Morbus Glanzmann

, 2010
In dieser Dissertation wurden drei hereditäre Krankheiten der primären Hämostase molekulargenetisch untersucht: Bernard-Soulier-Syndrom, Hermansky-Pudlak-Syndrom und Morbus Glanzmann.
Schäfer, Sophie
core  

Bernard-Soulier-like functional platelet defect in myelodysplastic syndrome and in acute myeloblastic leukemia associated with trilineage myelodysplasia

The Turkish Journal of Pediatrics, 1995
Platelet function was studied in a child with myelodysplastic syndrome (MDS: refractory anemia with an excess of blasts) and a child with acute myeloblastic leukemia (AML-M6) associated with trilineage myelodysplasia (TMDS).
G Hiçsönmez, F Gümrük, M Cetin, N Ozbek, M Tuncer, T Gürsel   +5 more
doaj