Literature DB >> 8216933

Primary T-cell immunodeficiencies.

A Fischer1.   

Abstract

The phenotypes of many primary T-cell immunodeficiencies have been described, including diseases associated with defective T-cell differentiation and/or activation. Recently, genotypes have been defined for some of them, such as X-linked severe combined immunodeficiency and CD3 deficiencies (or hyper IgM syndrome). Phenotype/genotype correlation studies open a fruitful way to a better understanding of primary T-cell immunodeficiencies.

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Year:  1993        PMID: 8216933     DOI: 10.1016/0952-7915(93)90040-y

Source DB:  PubMed          Journal:  Curr Opin Immunol        ISSN: 0952-7915            Impact factor:   7.486


  4 in total

1.  X-linked immune dysregulation, neonatal insulin dependent diabetes, and intractable diarrhoea.

Authors:  J E Peake; R B McCrossin; G Byrne; R Shepherd
Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  1996-05       Impact factor: 5.747

2.  A putative human equivalent of the murine Xlr (X-linked, lymphocyte-regulated) protein.

Authors:  B Allenet; D Escalier; H J Garchon
Journal:  Mamm Genome       Date:  1995-09       Impact factor: 2.957

Review 3.  Lymph node pathology in primary combined immunodeficiency diseases.

Authors:  F Facchetti; L Blanzuoli; M Ungari; O Alebardi; W Vermi
Journal:  Springer Semin Immunopathol       Date:  1998

Review 4.  Exploring the RNA Gap for Improving Diagnostic Yield in Primary Immunodeficiencies.

Authors:  Jed J Lye; Anthony Williams; Diana Baralle
Journal:  Front Genet       Date:  2019-12-11       Impact factor: 4.599

  4 in total

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