Literature DB >> 4175121

IgA deficiency: family studies.

C C Huntley, R L Stephenson.   

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Year:  1968        PMID: 4175121

Source DB:  PubMed          Journal:  N C Med J        ISSN: 0029-2559


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  6 in total

1.  The higher frequency of IgA deficiency among Swedish twins is not explained by HLA haplotypes.

Authors:  M Frankowiack; R-M Kovanen; G A Repasky; C K Lim; C Song; N L Pedersen; L Hammarström
Journal:  Genes Immun       Date:  2015-01-08       Impact factor: 2.676

2.  A hereditary immunoglobulin A abnormality: absence of light-heavy-chain assembly. Study of immunoglobulin synthesis in tonsillar cells.

Authors:  C Moroz; J Amir; A De Vries
Journal:  J Clin Invest       Date:  1971-12       Impact factor: 14.808

3.  Genetic linkage of IgA deficiency to the major histocompatibility complex: evidence for allele segregation distortion, parent-of-origin penetrance differences, and the role of anti-IgA antibodies in disease predisposition.

Authors:  I Vorechovský; A D Webster; A Plebani; L Hammarström
Journal:  Am J Hum Genet       Date:  1999-04       Impact factor: 11.025

4.  Human anti-IgM iso-antibodies in subjects with selective IgA deficiency.

Authors:  J V Wells; J F Bleumers; H H Fudenberg
Journal:  Clin Exp Immunol       Date:  1972-11       Impact factor: 4.330

5.  Cellular aspects of selective IgA deficiency.

Authors:  G Delespesse; P Gausset; C Cauchie; A Govaerts
Journal:  Clin Exp Immunol       Date:  1976-05       Impact factor: 4.330

6.  Genetic and immunologic analysis of a family containing five patients with common-variable immune deficiency or selective IgA deficiency.

Authors:  R F Ashman; F M Schaffer; J D Kemp; W M Yokoyama; Z B Zhu; M D Cooper; J E Volanakis
Journal:  J Clin Immunol       Date:  1992-11       Impact factor: 8.317

  6 in total

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