Literature DB >> 2323784

The "polyclonal hyperimmunoglobulin G1(A1) syndrome" is a secondary phenomenon due to autoimmune disease.

M J Krol-van Straaten, H C Haanen, C E de Maat.   

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Year:  1990        PMID： 2323784     DOI： 10.1007/bf00195829

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


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  3 in total

1.  IgG subclass levels in infancy and childhood.

Authors:  V A Oxelius
Journal:  Acta Paediatr Scand       Date:  1979-01

2.  An IgG subclass imbalance in connective tissue disease.

Authors:  R A Kay; K J Wood; R M Bernstein; P J Holt; R S Pumphrey
Journal:  Ann Rheum Dis       Date:  1988-07       Impact factor: 19.103

3.  Polyclonal hyper-immunoglobulin G1(A1) syndrome. Evidence for a dominant immunoglobulin production regulator within the human immunoglobulin heavy chain gene complex.

Authors:  R W Hendriks; L A Sandkuyl; M E Kraakman; G G de Lange; R K Schuurman
Journal:  Hum Genet       Date:  1989-05       Impact factor: 4.132
  3 in total

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