A Case of Blau Syndrome with NOD2 E383K Mutation. - Wikidata - wikimedia - TriplyDB

A Case of Blau Syndrome with NOD2 E383K Mutation.

A Case of Blau Syndrome with NOD2 E383K Mutation.

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Blau Syndrome: A Systemic Granulomatous Disease of Cutaneous Onset and Phenotypic Complexity.

P2860

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P2860

A Case of Blau Syndrome with NOD2 E383K Mutation.

http://www.wikidata.org/entity/Q51684483

description

2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年学术文章

@wuu

2016年学术文章

@zh

2016年学术文章

@zh-cn

2016年学术文章

@zh-hans

2016年学术文章

@zh-my

2016年学术文章

@zh-sg

2016年學術文章

@yue

2016年學術文章

@zh-hant

name

A Case of Blau Syndrome with NOD2 E383K Mutation.

@en

A Case of Blau Syndrome with NOD2 E383K Mutation.

@nl

type

label

A Case of Blau Syndrome with NOD2 E383K Mutation.

@en

A Case of Blau Syndrome with NOD2 E383K Mutation.

@nl

prefLabel

A Case of Blau Syndrome with NOD2 E383K Mutation.

@en

A Case of Blau Syndrome with NOD2 E383K Mutation.

@nl

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P1433

Pediatric Dermatology

P1476

A Case of Blau Syndrome with NOD2 E383K Mutation

@en

P2093

Jun Harada

http://www.w3.org/2001/XMLSchema#string

Takeshi Nakajima

http://www.w3.org/2001/XMLSchema#string

P2860

Autoinflammatory granulomatous diseases: from Blau syndrome and early-onset sarcoidosis to NOD2-mediated disease and Crohn's disease

Incomplete penetrance of the NOD2 E383K substitution among members of a pediatric granulomatous arthritis pedigree.

CARD15 mutations in Blau syndrome.

Role of the NOD2 genotype in the clinical phenotype of Blau syndrome and early-onset sarcoidosis.

Blau syndrome: cross-sectional data from a multicentre study of clinical, radiological and functional outcomes.

NOD2-associated pediatric granulomatous arthritis, an expanding phenotype: study of an international registry and a national cohort in Spain.

Caveats and truths in genetic, clinical, autoimmune and autoinflammatory issues in Blau syndrome and early onset sarcoidosis.

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e385-e387

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scholarly article

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10.1111/PDE.12908

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6

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33

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2016-06-24T00:00:00Z

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27339507

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