Screening assays for primary haemophagocytic lymphohistiocytosis in children presenting with suspected macrophage activation syndrome

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Screening assays for primary haemophagocytic lymphohistiocytosis in children presenting with suspected macrophage activation syndrome

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http://www.wikidata.org/entity/Q36287248

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2015 nî lūn-bûn

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2015年の論文

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年學術文章

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2015年學術文章

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2015年學術文章

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name

Screening assays for primary h ...... macrophage activation syndrome

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Screening assays for primary h ...... macrophage activation syndrome

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type

Item

label

Screening assays for primary h ...... macrophage activation syndrome

@ast

Screening assays for primary h ...... macrophage activation syndrome

@en

prefLabel

Screening assays for primary h ...... macrophage activation syndrome

@ast

Screening assays for primary h ...... macrophage activation syndrome

@en

P1476

Screening assays for primary h ...... macrophage activation syndrome

@en

P2093

Anupama Rao

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Despina Eleftheriou

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Kanchan Rao

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Kimberly Gilmour

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Mary Cruikshank

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Olga Nikolajeva

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Parameswaran Anoop

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Paul A Brogan

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P2860

Familial hemophagocytic lymphohistiocytosis type 5 (FHL-5) is caused by mutations in Munc18-2 and impaired binding to syntaxin 11

Macrophage activation syndrome in patients with systemic juvenile idiopathic arthritis is associated with MUNC13-4 polymorphisms

Natural killer cell dysfunction is a distinguishing feature of systemic onset juvenile rheumatoid arthritis and macrophage activation syndrome

Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene

Hematopoietic cell transplantation for hemophagocytic lymphohistiocytosis: a journey of a thousand miles begins with a single (big) step

Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type-4 to chromosome 6q24 and identification of mutations in syntaxin 11

Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome

Macrophage activation syndrome in juvenile systemic lupus erythematosus: a multinational multicenter study of thirty-eight patients.

Perforin gene defects in familial hemophagocytic lymphohistiocytosis.

Identification of the homologous beige and Chediak-Higashi syndrome genes.

P2888

s12969-015-0043-7

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scholarly article

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10.1186/S12969-015-0043-7

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P478

12 Suppl 1

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P577

2015-11-16T00:00:00Z

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P5875

284165221

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P6179

1040126686

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P698

26572973

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P921

macrophage

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4647814

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