Aberrant glycosylation of IgA1 is inherited in both pediatric IgA nephropathy and Henoch-Schönlein purpura nephritis

Kidney International

Volumn 80, Issue 1, 2011, Pages 79-87

  Kiryluk, Krzysztof ^a   Moldoveanu, Zina ^b   Sanders, John T ^c,d   Eison, T Matthew ^c,d   Suzuki, Hitoshi ^b,e   Julian, Bruce A ^b   Novak, Jan ^b   Gharavi, Ali G ^a   Wyatt, Robert J ^c,d  

^a Department of Neurology and the Taub Institute for Research on Alzheimer's Disease and the Aging Brain   (United States)

^b UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

^c UNIVERSITY OF TENNESSEE HEALTH SCIENCE CENTER   (United States)

^d LE BONHEUR CHILDREN S HOSPITAL   (United States)

^e JUNTENDO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

genetic renal disease; glomerular disease; glomerulonephritis; Henoch Sch nlein purpura; IgA nephropathy

Indexed keywords

GALACTOSE DEFICIENT IMMUNOGLOBULIN A1; IMMUNOGLOBULIN A1; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; ANAPHYLACTOID PURPURA; ARTICLE; CAUCASIAN; CHILD; CONTROLLED STUDY; DISEASE TRANSMISSION; ENZYME LINKED IMMUNOSORBENT ASSAY; ETHNICITY; FEMALE; GENETIC TRAIT; HERITABILITY; HUMAN; IMMUNOGLOBULIN A NEPHROPATHY; IMMUNOGLOBULIN BLOOD LEVEL; MAJOR CLINICAL STUDY; MALE; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL; PROTEIN GLYCOSYLATION; SCHOOL CHILD; SENSITIVITY AND SPECIFICITY;

EID: 79958856066     PISSN: 00852538     EISSN: 15231755     Source Type: Journal    
DOI: 10.1038/ki.2011.16     Document Type: Article

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