Results 61 to 70 of about 1,427 (117)

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  

Bernard-Soulier syndrome

Haematologica, 2011
Michael C. Berndt, Robert K. Andrews
doaj   +1 more source

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

Pregnancy Outcome in Bernard-Soulier Syndrome. [PDF]

J Obstet Gynaecol India, 2023
Durai V, Subburaj S, Subbaiah M.
europepmc   +1 more source

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  

Experience of kidney transplantation to a patient with Bernard Soulier syndrome: A case report. [PDF]

Turk J Surg, 2023
Karataş C, Akyollu B, Arpalı E, Yelken B, Türkmen A, Koçak B.   +5 more
europepmc   +1 more source

Characterization of zebrafish gp1ba mutant and modelling Bernard Soulier syndrome. [PDF]

Blood Coagul Fibrinolysis, 2022
Dhinoja S, Al Qaryoute A, Fallatah W, DeMaria A, Jagadeeswaran P.   +4 more
europepmc   +1 more source

Bernard-Soulier syndrome in pregnancy with retinal detachment: a rare phenomenon. [PDF]

BMJ Case Rep, 2022
Igbokwe N, Benson G, Waireri J.
europepmc   +1 more source

A GP1BA Variant in a Czech Family with Monoallelic Bernard-Soulier Syndrome. [PDF]

Int J Mol Sci, 2022
Skalníková M, Staňo Kozubík K, Trizuljak J, Vrzalová Z, Radová L, Réblová K, Holbová R, Kurucová T, Svozilová H, Štika J, Blaháková I, Dvořáčková B, Prudková M, Stehlíková O, Šmída M, Křen L, Smejkal P, Pospíšilová Š, Doubek M.   +18 more
europepmc   +1 more source