نتایج جستجو برای: glanzmann thrombasthenia

تعداد نتایج: 568  

Journal: :Indian Journal of Human Genetics 2010

Journal: :Pathophysiology of haemostasis and thrombosis 2002
Uri Seligsohn

Glanzmann thrombasthenia (GT) is an autosomal recessive bleeding disorder characterized by deficient or dysfunctional glycoprotein (GP) IIb/IIIa compexes. The hallmark of the disease is impaired platelet aggregation stemming from defective fibrinogen binding to GPIIb/IIIa. Based on deciphering the abnormality in GT a monoclonal antibody, peptides and peptidominetic agents, all interfering with ...

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...

2017
Ana R Cid Pau Montesinos Isabel Sánchez-Guiu Saturnino Haya Jose I Lorenzo Jaime Sanz Federico Moscardo Nieves Puig Dolores Planelles Santiago Bonanad Guillermo F Sanz Vicente Vicente Consuelo González-Manchón María L Lozano José Rivera Miguel A Sanz

Glanzmann thrombasthenia is a rare bleeding disorder that can present life-threatening bleeding. Our patients develop antiplatelet antibodies that become refractory to any pharmacological treatment. Allogeneic hematopoietic stem-cell transplantation is the only currently curative procedure, but has major risks mainly in adult; indeed, our patient died.

Journal: :International journal of laboratory hematology 2015
A Albanyan A Al-Musa R AlNounou H Al Zahrani R Nasr A AlJefri M Saleh A Malik H Masmali T Owaidah

BACKGROUND Glanzmann thrombasthenia (GT) is a rare inherited platelet disorder that is characterized by spontaneous or postprocedural bleeding. The diagnosis of GT depends on identifying the dysfunction of the platelets. AIM The aim of this study was to compare a whole blood impedance Multiplate analyzer (MEA) with the standard method, light transmission aggregometry (LTA) in diagnosis of GT....

2006
Asier Jayo Dina Pabón Pedro Lastres Victor Jiménez Consuelo González-Manchón

Glanzmann thrombasthenia is an autosomal recessive bleeding disorder characterized by a life-long hemorrhagic tendency and absent or severely reduced platelet aggregation in response to agonists. The thrombasthenic phenotype is associated with quantitative or qualitative abnormalities in the platelet fibrinogen receptor, the αIIbβ3 integrin or glycoprotein (GP) IIb-IIIa, which can also serve as...

Journal: :Journal of South Asian Federation of Obstetrics and Gynaecology 2019

Journal: :The British journal of general practice : the journal of the Royal College of General Practitioners 2002
Adrian Kay

The general practitioner (GP) fundholding scheme was introduced as part of the Conservative governments 1991 National Health Service reforms and abolished by the Labour government in 1998. This paper contends that the scheme was introduced and abolished without policy-makers having any valid evidence of its effects. In particular, it focuses on the salient features of the decision to abolish. T...

Journal: :European Journal of Human Genetics 2012

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