نتایج جستجو برای: primary immunodeficiency diseases pid

تعداد نتایج: 1504298  

2017
Jeevani Kumarage Suranjith L. Seneviratne Vijitha Senaratne Amitha Fernando Kirthi Gunasekera Bandu Gunasena Padmalal Gurugama Sudath Peiris Antony R. Parker Stephen Harding Nilhan Rajiva de Silva

Measurement of an individuals ability to respond to polysaccharide antigens is a crucial test to determine adaptive immunity. Currently the response to Pneumovax® is utilized but with the success of Prevnar®, measurement of the response to Pneumovax may be challenging. The aim of the study was to assess the response to Typhi Vi vaccination in both children and adult control groups and patients ...

2017
Asghar Aghamohammadi Hassan Abolhassani Necil Kutukculer Steve G. Wassilak Mark A. Pallansch Samantha Kluglein Jessica Quinn Roland W. Sutter Xiaochuan Wang Ozden Sanal Tatiana Latysheva Aydan Ikinciogullari Ewa Bernatowska Irina A. Tuzankina Beatriz T. Costa-Carvalho Jose Luis Franco Raz Somech Elif Karakoc-Aydiner Surjit Singh Liliana Bezrodnik Francisco J. Espinosa-Rosales Anna Shcherbina Yu-Lung Lau Shigeaki Nonoyama Fred Modell Vicki Modell Mohamed-Ridha Barbouche Mark A. McKinlay

Immunodeficiency-associated vaccine-derived polioviruses (iVDPVs) have been isolated from primary immunodeficiency (PID) patients exposed to oral poliovirus vaccine (OPV). Patients may excrete poliovirus strains for months or years; the excreted viruses are frequently highly divergent from the parental OPV and have been shown to be as neurovirulent as wild virus. Thus, these patients represent ...

2011
Sasawan Chinratanapisit Panida Sriaroon

Primary and secondary immunodeficiency disorders are a diverse group of illnesses resulting from one or more abnormalities of the immune system. The clinical manifestations include increased susceptibility to infection and an increased risk for autoimmune disease and malignancy. Primary immune deficiency (PID) diseases are a group of serious disorders arising from an intrinsic defect in the imm...

2009
Teresa Espanol

Primary immunodeficiencies (PID) are inherited disorders of immune system function [1,2] characterised by absent or low response to infectious agents and a high prevalence of autoimmune manifestations and lymphoproliferative diseases. More than 120 PID in which a molecular defect causes the disease have been identified. The IUIS/WHO Experts Committee published a classification of all PID known ...

2014
O. Jilkina J.R. Thompson L. Kwan P. Van Caeseele C. Rockman-Greenberg M.L. Schroeder

In Manitoba, Canada, the overall incidence of Severe Combined Immunodeficiency (SCID) is three-fold higher than the national average, with SCID overrepresented in two population groups: Mennonites and First Nations of Northern Cree ancestries. T-cell receptor excision circle (TREC) assay is being used increasingly for neonatal screening for SCID in North America. However, the majority of SCID p...

Abdolreza Malek, Hamid Ahanchian, Mehrdad Sarabi, Nasrin Moazzen, Zahra Abbasi Shaye,

Primary Immune Deficiencies are a group of heterogeneous disorders that involve the innate or acquired immune system, or a combination of them. The underlying disorder may be related to decreased levels or function, or a complete lack of one or more components of the immune system in general. These diseases can occur with a prevalence of about 1 in 10000 live births. According to the fourth upd...

2015
Morvarid Oveisi Oriyah Barzilay Ahmed A. Hanafi

Primary immunodeficiency diseases are rare hereditary conditions that usually occur at a young age; however, secondary immunodeficiency is acquired due to disease, drug treatment and is increasing in frequency among the population. Although periodontal diseases related to these conditions are secondary to other life threatening manifestations, they are very common and easily detectable by the p...

Journal: :European annals of allergy and clinical immunology 2014
D Tirotta V Durante

Common Variable Immunodeficiency (CVID) is one of the most common causes of Primary Immunodeficiency Disorders (PIDs) and of Primary Hypogammaglobulinemia in adulthood. Clinical features include variable combinations of infectious diseases, autoimmune diseases, lymphoproliferative disorders and gastrointestinal diseases. In this case report, delayed detection of the disease had a negative progn...

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