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Search Results for "Adamts13 Deficiency And Iga Deficiency"

23:07 EDT 24th May 2013 | BioPortfolio

Original Source: Selective IgA Deficiency: Clinical and Laboratory Features of 118 Children in Turkey.

Selective IgA deficiency (IgAD) is considered as the most common primary immunodeficiency. Although the vast majority of affected individuals are asymptomatic, symptomatic patients suffer from recurrent infections, allergies and autoimmune diseases. In the present study, we aimed to investigate the clinical and laboratory features of children with IgAD in a tertiary children's hospital in Turkey. The medical records of 118 patients (63 males, 55 females) aged 4-18 years (median: 7 years) seen from 2006 to...

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Vitamin E Deficiency

Frank vitamin E deficiency is rare and overt deficiency symptoms have not been found in healthy people who obtain little vitamin E from their diets. Premature babies of very low birth weight (<1,...

IgA Deficiency

Deficiency

Vitamin B12 Deficiency

Iron deficiency

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Vitamin B12 Deficiency Prevalent Among Refugees

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Vitamin D deficiency may contribute to alcohol-related muscular weakness

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Vitamin D Deficiency An Increased Risk In Obesity

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Diagnosis and treatment of growth hormone deficiency in adults

Adult growth hormone (GH) deficiency is now recognized as a distinct if nonspecific syndrome with considerable adverse health consequences. This Review outlines the physiological regulation and nonsta...

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Mild vitamin B12 deficiency associated with accelerated cognitive decline

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Prevalence and Predictors of Vitamin D Deficiency in Adults

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Clinical features of severe acquired ADAMTS13 deficiency in thrombotic thrombocytopenic purpura: the Korean TTP registry experience.

The clinical significance of ADAMTS13 activity for response to treatment, mortality rate, recurrence, and prognosis is unclear. Therefore, we investigated the characteristics of severe ADAMTS13 defici...

Ten patient stories illustrating the extraordinarily diverse clinical features of patients with thrombotic thrombocytopenic purpura and severe ADAMTS13 deficiency.

Patients with thrombotic thrombocytopenic purpura (TTP) and severe ADAMTS13 deficiency are often considered to have typical clinical features. However, our experience is that there is extraordinary di...

How I treat patients with thrombotic thrombocytopenic purpura - 2010.

Thrombotic thrombocytopenic purpura (TTP) is the common name for adults with microangiopathic hemolytic anemia, thrombocytopenia, with or without neurologic or renal abnormalities, and without another...

Thrombospondin-1 and ADAMTS13 competitively bind to VWF A2 and A3 domains in vitro.

INTRODUCTION: ADAMTS13 (a disintegrin-like and metalloprotease with thrombospondin type 1 repeat motif. 13) is the major metalloprotease for VWF degradation. ADAMTS13 deficiency causes the accumulatio...

Usefulness of antithrombin deficiency phenotypes for risk assessment of venous thromboembolism: type I deficiency as a strong risk factor for venous thromboembolism.

Inherited antithrombin deficiency, an established risk factor for venous thromboembolism (VTE), can be classified into type I (quantitative deficiency) or type II (qualitative deficiency). In the pres...

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