نتایج جستجو برای: agammaglobulinemia

تعداد نتایج: 619  

2010
Phenix-Lan Quan Thor A. Wagner Thomas Briese Troy R. Torgerson Mady Hornig Alla Tashmukhamedova Cadhla Firth Gustavo Palacios Ada Baisre-De-Leon Christopher D. Paddock Stephen K. Hutchison Michael Egholm Sherif R. Zaki James E. Goldman Hans D. Ochs W. Ian Lipkin

Encephalitis is a major cause of death worldwide. Although >100 pathogens have been identified as causative agents, the pathogen is not determined for up to 75% of cases. This diagnostic failure impedes effective treatment and underscores the need for better tools and new approaches for detecting novel pathogens or determining new manifestations of known pathogens. Although astroviruses are com...

Journal: :Anales de pediatria 2015
A Fernandes M Guedes J Vasconcelos E Neves S Fernandes L Marques

INTRODUCTION X-Linked agammaglobulinemia (XLA) is characterized by an arrest of B cell differentiation, leading to recurrent bacterial infections. Lifelong immunoglobulin replacement therapy (IRT) is indicated to prevent infections and their complications. MATERIAL AND METHODS A retrospective study of patients with XLA followed in a level three hospital was performed; data was collected retro...

Journal: :Journal of immunology 1985
M E Conley

X-linked agammaglobulinemia (XLA) has been described as a disorder in which pre-B cells fail to differentiate into B cells. However, a small number of B cells have been seen occasionally in patients with this disorder. Because the phenotype of these cells might be helpful in defining the site of the defect in XLA, immunofluorescent staining techniques were used to characterize the B cells that ...

Journal: :iranian journal of allergy, asthma and immunology 0
bahram mir saeid ghazi asghar aghamohammadi ali kouhi abolhassan farhoudi mostafa moin nima rezaei

primary immunodeficiencies (pid) are a group of disorders, characterized by an unusual susceptibility to infections. delay in diagnosis results in increased morbidity and mortality in affected patients. the purpose of this study was to determine the mortality rate of iranian immunodeficient patients referred to children medical center hospital affiliated to tehran university of medical sciences...

Journal: :iranian journal of immunology 0
asghar aghamohammadi department of clinical pediatric immunology, children's medical center hospital, tehran university of medical sciences, tehran, iran ali akbar amirzargar department of immunogenetics, tehran university of medical sciences, tehran, iran nima parvaneh department of clinical pediatric immunology, children's medical center hospital, tehran university of medical sciences, tehran, iran paul marjousef department of immunogenetics, tehran university of medical sciences, tehran, iran mostafa moin department of clinical pediatric immunology, children's medical center hospital, tehran university of medical sciences, tehran, iran abdolhassan farhoudi department of clinical pediatric immunology, children's medical center hospital, tehran university of medical sciences, tehran, iran mehdi yeganeh

background: the b-cell defect in x-linked agammaglobulinemia (xla) is caused by mutations in the gene for bruton's tyrosine kinase (btk). btk mutations result in deficient expression of btk protein in peripheral blood monocytes. methods: using the anti-btk monoclonal antibody (48-2h), a flow cytometric analysis of intra cytoplasmic btk protein expression in monocytes was performed to ident...

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