Results 151 to 160 of about 3,107 (209)

Diagnostic and therapeutic challenges in rare hematologic entities: monoclonal gammopathy of thrombotic and bleeding significance. [PDF]

Haematologica
Fotiou D, Antic D, Delluc A, Sanfilippo KM, Terpos E, Kastritis E, Gkalea V.   +6 more
europepmc   +1 more source

Management challenge of a rare concomitant platelet glycoprotein IV/CD36 and IIb/IIIa deficiencies: Case illustration. [PDF]

Transfusion
Sekayan T, Allen ES, Kopko P, Stephens LD, Zhao M, Curtis BR, Sullivan MJ, Trapp-Stamborski V, von Drygalski A.   +8 more
europepmc   +1 more source

A Novel Variant of the FERMT3 Gene Associated With Leukocyte Adhesion Deficiency Type III (LAD-III) in a Saudi Family: A Case Series. [PDF]

Cureus
Alasmari BG, Alghubishi SA, Rayees S, AlDahmashi AS, Alamri SS, Al Zahrani D.   +5 more
europepmc   +1 more source

A case of thrombasthenia.

The Ceylon medical journal, 1971
openaire   +1 more source

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Glanzmann’s Thrombasthenia

The Indian Journal of Pediatrics, 2001
Glanzmann's thrombasthenia (GT) is an uncommon cause of bleeding in children. We diagnosed two siblings as having GT on the basis of flow cytometric studies. Both had cutaneous bleedings and epistaxis since early childhood. Hematological investigations revealed prolonged bleeding time and a normal platelet count.
M S, Tullu, P S, Dixit, S B, Nair, J R, Kamat, R K, Vaswani, S D, Shetty, A R, Pawar   +6 more
openaire   +2 more sources

Endometriosis in two sisters with Glanzmann's thrombasthenia

Fertility and Sterility, 2009
Objective: To present two cases of endometriosis in patients with Glanzmann's thrombasthenia (GT) and discuss the underlying pathophysiology of endometriosis. Design: Case report. Setting: Gynecology practice in a university teaching hospital. Patient(s):
Erkan Alatas, Sibel Hacioğlu
exaly   +2 more sources

The use of recombinant factor VIIa in a primigravida with Glanzmann’s thrombasthenia during delivery

Journal of Perinatal Medicine, 2004
Glanzmanns thrombasthenia is an inherited hemorrhagic disorder characterized by a severe reduction in, or absence of, platelet aggregation in response to multiple physiologic agonists due to qualitative or quantitative abnormalities of platelet ...
Bayhan, G, Kale, A, Yalinkaya, A, Yayla, M   +3 more
exaly   +2 more sources

Thrombasthenia in Liver Disease

New England Journal of Medicine, 1961
IMPAIRMENT of the hemostatic mechanism is a common experience in active disease of the liver. Several recent reports1 2 3 4 have stressed the multiplicity of plasma clotting factors that may be deficient, as well as the frequency of reduction in the number of platelets.
E E, MANDEL, J, LAZERSON
openaire   +2 more sources

A Variant Form of Thrombasthenia

Archives of Pediatrics & Adolescent Medicine, 1991
We encountered two siblings with abnormal bruising since infancy. Studies revealed functional platelet defects characterized by a lack of platelet aggregation and adenosine triphosphate release on exposure to adenosine diphosphate and collagen as well as variable responses with ristocetin (at concentrations of less than or equal to 1.25 g/L) and ...
M D, Tarantino, J J, Corrigan, L, Glasser, C M, Payne, M A, Jeter   +4 more
openaire   +2 more sources

PSEUDOHEMOPHILIA OR CHRONIC THROMBASTHENIA

Archives of Surgery, 1949
THE CONDITIONS under discussion are those which have been called in the literature "pseudohemophilia or chronic hereditary thrombasthenia." These two dyscrasias were originally described nearly forty years ago, but it has only been in recent years that a clear differentiation has been drawn between the two entities and their characteristics more ...
openaire   +2 more sources