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1. 若年性特発性関節炎：疫学と免疫病態学 juvenile idiopathic arthritis epidemiology and immunopathogenesis

English Journal

Macrophage activation syndrome: advances towards understanding pathogenesis.

Grom AA, Mellins ED.SourceDivision of Pediatric Rheumatology, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA. Alexei.Grom@cchmc.org
Current opinion in rheumatology.Curr Opin Rheumatol.2010 Sep;22(5):561-6.
PURPOSE OF REVIEW: Macrophage activation syndrome (MAS), a major cause of morbidity and mortality in pediatric rheumatology, is most strongly associated with systemic juvenile idiopathic arthritis (SJIA). There are no validated diagnostic criteria and early diagnosis is difficult. This review summar
PMID 20517154

STX11 mutations and clinical phenotypes of familial hemophagocytic lymphohistiocytosis in North America.

Marsh RA, Satake N, Biroschak J, Jacobs T, Johnson J, Jordan MB, Bleesing JJ, Filipovich AH, Zhang K.SourceDivision of Bone Marrow Transplant and Immune Deficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio 45229, USA. rebecca.marsh@cchmc.org
Pediatric blood & cancer.Pediatr Blood Cancer.2010 Jul 15;55(1):134-40.
BACKGROUND: Mutations in STX11 are responsible for Familial Hemophagocytic Lymphohistiocytosis (FHLH) type 4, a rare primary immunodeficiency which has previously been observed only in patients of Kurdish, Turkish, and Lebanese ethnic background.METHODS: We reviewed our experience with STX11 mutatio
PMID 20486178

Japanese Journal

Further evidence for genetic heterogeneity in familial hemophagocytic lymphohistiocytosis (FHLH)

GRAHAM GE
Pediatr Res. 48, 227-232, 2000
NAID 30027175670

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