Results 11 to 20 of about 3,107 (209)
The international, prospective Glanzmann Thrombasthenia Registry: treatment modalities and outcomes of non-surgical bleeding episodes in patients with Glanzmann thrombasthenia [PDF]
Haematologica, 2015 Standard treatment for Glanzmann thrombasthenia is platelet transfusion. Recombinant activated factor VII has been shown to be successful in patients with Glanzmann thrombasthenia with platelet antibodies or who are refractory to platelet transfusions ...
Giovanni Di Minno +5 more
doaj +2 more sources
Glanzmann thrombasthenia [PDF]
Orphanet Journal of Rare Diseases, 2006 Glanzmann thrombasthenia (GT) is a rare autosomal recessive bleeding syndrome affecting the megakaryocyte lineage and characterized by lack of platelet aggregation.
Nurden Alan T
doaj +3 more sources
African Journal of Paediatric Surgery, 2016 Glanzmann's thrombasthenia (GT) is a rare autosomal recessive disorder in which the platelets have anomalies of fibrinogen receptors causing bleeding tendencies.
Iftikhar Ahmad Jan +4 more
doaj +2 more sources
Glanzmann Thrombasthenia Associated with Siderotic Synovitis and Arthropathy: A Case Report
Journal of Blood Medicine, 2023 Mouhammad J Alawad,1 Mohammad Abu-Tineh,2 Awni Alshurafa,2 Alaa Al-Taie,3 Anil Yousaf,2 Mohamed A Yassin2 1Department of Medical Education, Internal Medicine Residency Program, Hamad Medical Corporation, Doha, Qatar; 2Department of Medical Oncology ...
Alawad MJ +5 more
doaj +1 more source
Glanzmann thrombasthenia: An update
Clinica Chimica Acta, 2010 Glanzmann thrombasthenia (GT) is a rare autosomal recessive disorder characterized by qualitative or quantitative abnormalities of the platelet membrane glycoprotein (GP) IIb/IIIa. Physiologically, this platelet receptor normally binds several adhesive plasma proteins, and this facilitates attachment and aggregation of platelets to ensure thrombus ...
Franchini M +2 more
openaire +4 more sources
GLANZMANNS THROMBASTHENIA [PDF]
Basrah Journal of Surgery, 2009 Tolosa-Hunt syndrome (THS) has been described as a painful, unilateral, partial or total ophthalmoplegia caused by a nonspecific granulomatous process in the cavernous sinus, the superior orbital fissure, or the orbital apex.
ZUHAIR AL-BARAZANCHImad
doaj +3 more sources
Hematological and surgical management in Glanzmann′s thrombasthenia: A case report
Journal of Indian Society of Pedodontics and Preventive Dentistry, 2014 Glanzmann′s thrombasthenia (GT) is a rare, congenital, and moderate to severe platelet disorder. The bleeding time is increased, due to lack of platelet aggregation, since the patients with GT have deficient or dysfunctional integrin membrane ...
Anjana Gopalakrishnan +2 more
doaj +2 more sources
Glanzmann thrombasthenia associated with human immunodeficiency virus-positive patient
International Journal of Preventive Medicine, 2014 Glanzmann′s thrombasthenia (GT) is an autosomal recessive inherited platelet function defect characterized by normal platelet count, prolonged bleeding time and abnormal clot retraction.
Rakesh Kumar Manne +5 more
doaj +1 more source
Glanzmann′s thrombasthenia associated with HBsAg-positive child: A case report
Journal of Indian Society of Pedodontics and Preventive Dentistry, 2007 Glanzmann′s thrombasthenia is a rare hemorrhagic disorder characterized by prolonged bleeding time and diminished clot retraction. The disease is marked by frequent mucocutaneous hemorrhage which is mainly due to qualitative defects of platelets ...
Poornima G, Shivaprasad S, Ashok L
doaj +1 more source
Glanzmann's thrombasthenia: pathogenesis, diagnosis, and current and emerging treatment options
Journal of Blood Medicine, 2015 Tia Solh,1 Ashley Botsford,2 Melhem Solh31Department of Physician Assistant Studies, Philadelphia College of Osteopathic Medicine, Suwanee, GA, USA; 2College of Health Care Sciences, Nova Southeastern University, Orlando, FL, USA; 3The Blood and Marrow ...
Solh T, Botsford A, Solh M
doaj +1 more source