نتایج جستجو برای: glanzmanns thrombasthenia

تعداد نتایج: 525  

Journal: :British journal of haematology 2002
Isabelle Martin Fayçal Kriaa Valérie Proulle Benoît Guillet Cécile Kaplan Roseline D'Oiron Marianne Debré Edith Fressinaud Yyes Laurian Gil Tchernia Bernard Charpentier Thierry Lambert Marie Dreyfus

Type I Glanzmann's thrombasthenia is a rare congenital platelet function disorder, characterized by undetectable platelet membrane glycoprotein IIb-IIIa (GPIIb-IIIa). Severe bleeding is controlled by transfusion of normal platelets, leading in some cases to the occurrence of anti-GPIIb-IIIa isoantibodies, which induces a loss of transfused platelet efficacy. We used immunoadsorption on protein ...

2002
O. Shpilberg I. Rabi R. Walden D. Harats K. S. Tyrrell B. Coller U. Seligsohn

Background—Platelets have been suggested to play a role in the early development of atherosclerosis. As one test of this hypothesis, we assessed whether patients with Glanzmann thrombasthenia who lack platelet glycoprotein IIb 3 (GPIIb/IIIa) complexes or both IIb 3 and the more ubiquitous v 3 cell membrane complexes are protected from development of atherosclerosis. Methods and Results—Seven pa...

Journal: :Journal of the College of Physicians and Surgeons--Pakistan : JCPSP 2016
Irem Iqbal Saima Farhan Nisar Ahmed

OBJECTIVE To describe the clinical presentation of patients with Glanzmann's thrombasthenia (GT) and evaluate their diagnostic, clinical, and laboratory parameters including platelet aggregometry. STUDY DESIGN Descriptive study. PLACE AND DURATION OF STUDY Department of Hematology and Blood Transfusion, The Children Hospital and Institute of Child Health, Lahore, from January 2006 to Decemb...

Journal: :The Israel Medical Association journal : IMAJ 2014
Dorit Blickstein Rima Dardik Esther Rosenthal Judith Lahav Yair Molad Aida Inbal

BACKGROUND A 75 year old patient presenting with mucocutaneous bleeding was diagnosed with acquired thrombasthenia. The diagnosis was based on lack of platelet aggregation with adenosine diphosphate (ADP), arachidonic acid and collagen, and normal aggregation induced by ristocetin. OBJECTIVE To study the mechanism of platelet function inhibition in a patient with acquired thrombasthenia. ME...

Journal: :Blood 1972
F Booyse D Kisieleski R Seeler M Rafelson

Journal: :international journal of preventive medicine 0
rakesh kumar manne kannan natarajan rajendra patil venkata sarath prathi beeraka swapna suneel kumar k.v

glanzmann’s thrombasthenia (gt) is an autosomal recessive inherited platelet function defect characterized by normal platelet count, prolonged bleeding time and abnormal clot retraction. this disease typically presents in infancy or early childhood and has proven to have very good prognosis. in this case study, a 22‑year‑old gt patient who also developed human immunodeficiency virus (hiv) infec...

Journal: :Haematologica 2015
Veronika Navrkalova Leona Raskova Kafkova Vladimir Divoky Sarka Pospisilova

Editorials 989 Precision medicine in diffuse large B-cell lymphoma: hitting the target Joost S. Vermaat, et al. Guideline Article 997 Consensus recommendations for the diagnosis and management of hemophagocytic lymphohistiocytosis associated with malignancies Kai Lehmberg, et al. Articles Hematopoiesis 1005 TIMP-1 signaling via CD63 triggers granulopoiesis and neutrophilia in mice Julia Kobuch,...

Journal: :Indian Journal of Case Reports 2019

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