Molecular genetic investigation, clinical features and response to treatment in 21 patients with Schnitzler's syndrome.

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Molecular genetic investigation, clinical features and response to treatment in 21 patients with Schnitzler's syndrome.

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http://www.wikidata.org/entity/Q47248926

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2017 nî lūn-bûn

@nan

2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

@zh-my

2017年学术文章

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2017年學術文章

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2017年學術文章

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2017年學術文章

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name

Molecular genetic investigatio ...... ts with Schnitzler's syndrome.

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Molecular genetic investigatio ...... ts with Schnitzler's syndrome.

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Molecular genetic investigatio ...... ts with Schnitzler's syndrome.

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type

Item

label

Molecular genetic investigatio ...... ts with Schnitzler's syndrome.

@en

Molecular genetic investigatio ...... ts with Schnitzler's syndrome.

@en-gb

Molecular genetic investigatio ...... ts with Schnitzler's syndrome.

@nl

prefLabel

Molecular genetic investigatio ...... ts with Schnitzler's syndrome.

@en

Molecular genetic investigatio ...... ts with Schnitzler's syndrome.

@en-gb

Molecular genetic investigatio ...... ts with Schnitzler's syndrome.

@nl

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2-s2.0-85047558213

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Blood

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Molecular genetic investigatio ...... ts with Schnitzler's syndrome.

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Anna Baginska

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Ashutosh D Wechalekar

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Dan Lipsker

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Dorota M Rowczenio

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Ebun Omoyinmi

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Hadija Trojer

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Julian D Gillmore

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Paul Brogan

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Philip N Hawkins

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Rene Williams

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P2860

Schnitzler's syndrome: lessons from 281 cases

The NLRP3 inflammasome is released as a particulate danger signal that amplifies the inflammatory response

Interleukins and interleukin receptors in rheumatoid arthritis: Research, diagnostics and clinical implications.

An update on autoinflammatory diseases

The Schnitzler syndrome.

Efficacy and safety of rilonacept (interleukin-1 Trap) in patients with cryopyrin-associated periodic syndromes: results from two sequential placebo-controlled studies.

Use of canakinumab in the cryopyrin-associated periodic syndrome.

Brief Report: Cryopyrin-Associated Periodic Syndrome Caused by a Myeloid-Restricted Somatic NLRP3 Mutation.

The role of interleukin 6 in the pathophysiology of rheumatoid arthritis

Clinical characteristics in subjects with NLRP3 V198M diagnosed at a single UK center and a review of the literature.

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974-981

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scholarly article

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10.1182/BLOOD-2017-10-810366

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English

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1100121146

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2778566674

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