Autoimmune haemolytic anaemia in a child with MHC class II deficiency.

Author:

Horneff G,Seitz R C,Stephan V,Wahn V

Publisher

BMJ

Subject

Pediatrics, Perinatology and Child Health

Reference15 articles.

1. Combined immunodeficiency disease associated with absence of cell surface HLA A and B antigens;Touraine, J.L.; Betuel, H.; Suillet, G.; Jeune, M.;JPediatr,1978

2. Combined immunodeficiency with abnormal expression of MHC class II genes;Griscelli, C.; Lisowska-Grospierre, B.; LeDeist, F.;Clin Immunol Immunopathol,1989

3. Activation of genetically major histocompatibility complex (MHC) class II deficient B lymphocytes;Durandy, A.; Mangeney, M.; Griscelli, C.; Forveille, M.; LeDeist, F.; Fischer, A.;Clin Immunol,1989

4. Seltener primarer Immundefekt. Major-HistocompatibilityComplex-Klasse II Antigendefekt;Remy, N.; Grundhewer, H.; Stuck, B.; Wahn, U.;Padiatrische Praxis,1991

5. A defect in the regulation of major histocompatibility complex class II gene expression in human HLA-DR negative lymphocytes from patients with combined immunodeficiency syndrome;Lisowska-Grospierre, B.; Charron, D.J.; DePreval, C.; Durandy, A.; Griselli, C.; Mach, B.,1985

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