نتایج جستجو برای: agammaglobulinemia

تعداد نتایج: 619  

Journal: :World Allergy Organization Journal 2012

Journal: :Pediatrics 2015
Kahn Preece Graeme Lear

We present a 22-month-old boy with X-linked agammaglobulinemia masked by normal immunoglobulin levels and vaccine seroconversion. Diagnosis was made after strong clinical suspicion of immune deficiency led to identification of markedly reduced B-cell numbers and confirmation with identification of a novel Bruton tyrosine kinase gene mutation. He was commenced on replacement immunoglobulin thera...

Journal: :Frontiers in bioscience : a journal and virtual library 1997
M Vihinen P T Mattsson C I Smith

X-linked agammaglobulinemia (XLA) is a heritable immunodeficiency disorder that is caused by a differentiation block leading to almost complete absence of B lymphocytes and plasma cells. The affected protein is a cytoplasmic protein tyrosine kinase, Bruton's agammaglobulinemia tyrosine kinase (Btk). Btk along with Tec, Itk and Bmx belong to a distinct family of protein kinases. These proteins c...

2002
Michael P. Okoh Mauno Vihinen

Academic dissertation To be presented for public criticism, with the permission of Abbreviations Abstract 1 Introduction 10 1.1 Primary immunodeficiencies (PIDs) 10 1.1.1 X-linked agammaglobulinemia (XLA) 12

Journal: :The Tohoku Journal of Experimental Medicine 1986

Journal: :The Journal of clinical investigation 2013
Bertrand Boisson Yong-Dong Wang Amma Bosompem Cindy S Ma Annick Lim Tatiana Kochetkov Stuart G Tangye Jean-Laurent Casanova Mary Ellen Conley

Approximately 90% of patients with isolated agammaglobulinemia and failure of B cell development have mutations in genes required for signaling through the pre–B cell and B cell receptors. The nature of the gene defect in the majority of remaining patients is unknown. We recently identified 4 patients with agammaglobulinemia and markedly decreased numbers of peripheral B cells. The B cells that...

2017
Marilia Pyles P. Kanegae Lucila Akune Barreiros Jusley Lira Sousa Marco Antônio S. Brito Edgar Borges de Oliveira Lara Pereira Soares Juliana Themudo L. Mazzucchelli Débora Quiorato Fernandes Sonia Marchezi Hadachi Silvia Maia Holanda Flavia Alice T. M. Guimarães Maura Aparecida P. V. V. Boacnin Marley Aparecida L. Pereira Joaquina Maria C. Bueno Anete Sevciovic Grumach Regina Sumiko W. Di Gesu Amélia Miyashiro N. dos Santos Newton Bellesi Beatriz T. Costa-Carvalho Antonio Condino-Neto

OBJECTIVE To validate the quantification of T-cell receptor excision circles (TRECs) and kappa-deleting recombination excision circles (KRECs) by real-time polymerase chain reaction (qRT-PCR) for newborn screening of primary immunodeficiencies with defects in T and/or B cells in Brazil. METHODS Blood samples from newborns and controls were collected on filter paper. DNA was extracted and TREC...

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