نتایج جستجو برای: protein deficiency

تعداد نتایج: 1343851  

Journal: :iranian journal of blood and cancer 0

introduction: megaloblasc anemia is an uncommon problem in childhood most frequently associated with vitamin deficiency or gastrointesnal disease. the common causes of megaloblasc anemia are vitamin b12 (cobalamin) deficiency and folic acid deficiency. familial selecve malabsorpon of vitamin b12 associated with proteinuria firstly was described by imerslund (1960) and grasbeck et al (1960)...

Journal: :iranian journal of diabetes and obesity 0
jaydip ray chaudhuri department of neurology, yashoda hospital hyderabad-500082, india. k rukmini mridula department of neurology, nizams’s institute of medical sciences hyderabad-500082, india amidyala lingaiah director of medical services, yashoda hospital, hyderabad -500082, india. banda balaraju department of medicine, yashoda hospital, hyderabad -500082, india. srinivasarao vcsbandaru department of neurology, yashoda hospital hyderabad-500082, india.-department of research, yashoda hospital, hyderabad -500082, india

objective: vitamin d deficiency is a common disorder worldwide and is indicated by low serum 25-hydroxyvitamin d levels. recent studies have suggested an association of 25-hydroxyvitamin d deficiency with diabetes mellitus. the objective of this study is to investigate the relationship between 25-hydroxyvitamin d concentration and type 2 diabetes in south indian patients. materials and methods:...

Journal: :Haematologica 2010
Elisabetta Castoldi Lisbeth F A Maurissen Daniela Tormene Luca Spiezia Sabrina Gavasso Claudia Radu Tilman M Hackeng Jan Rosing Paolo Simioni

BACKGROUND Protein S, which circulates in plasma in a free and bound form, is an anticoagulant protein that stimulates both activated protein C (APC) and tissue factor pathway inhibitor (TFPI). Hereditary type I protein S deficiency (low total and low free protein S) is a well-established risk factor for venous thrombosis, whereas the thrombosis risk associated with type III deficiency (normal ...

Journal: :Haematologica 2014
Hee-Jin Kim Ja-Young Seo Ki-O Lee Sung-Hwan Bang Seung-Tae Lee Chang-Seok Ki Jong-Won Kim Chul Won Jung Duk-Kyung Kim Sun-Hee Kim

Hereditary natural anticoagulant deficiencies are the major cause of genetic thrombophilia in Asia. Given the growing acknowledgment of the risk of venous thromboembolism in Asian populations, we investigated the frequency and mutation spectrums of natural anticoagulant deficiency in Korea. The group of patients consisted of consecutive patients with venous thromboembolism screened for thrombop...

Journal: :Journal of the Royal Society of Medicine 1990

Journal: :Indian Journal of Dermatology, Venereology, and Leprology 2012

Journal: :Journal of Nepal Medical Association 2010

Journal: :Journal of Stem Cell Research & Therapeutics 2016

2010
Sabine Kroiss Manuela Albisetti

Protein C is one of the major inhibitors of the coagulation system that downregulate thrombin generation. Severe congenital protein C deficiency leads to a hypercoagulability state that usually presents at birth with purpura fulminans and/or severe venous and arterial thrombosis. Recurrent thrombotic events are commonly seen. From the 1990's, several virus-inactivated human protein C concentrat...

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