(Q40102364)

17 September 2017

Brief Report: Late-Onset Cryopyrin-Associated Periodic Syndrome Due to Myeloid-Restricted Somatic NLRP3 Mosaicism (English)

1 reference

cryopyrin-associated periodic syndrome

17 September 2017

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author

Anna Mensa-Vilaro

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27273849%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

Giuliana Magri

3

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Helios Martínez-Banaclocha

8 June 2020

5

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8 June 2020

Jordi Sintes

7

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8 June 2020

Eva Gonzalez-Roca

8

1 reference

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Juan José Martínez-García

8 June 2020

11

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8 June 2020

Alberto Baroja-Mazo

12

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8 June 2020

Andrea Cerutti

13

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8 June 2020

Ryuta Nishikomori

14

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8 June 2020

Pablo Pelegrín

16

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8 June 2020

Juan I Arostegui

18

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8 June 2020

author name string

María Teresa Bosque

2

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8 June 2020

Yoshitaka Honda

4

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8 June 2020

Marta Casorran-Berges

6

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8 June 2020

Estibaliz Ruiz-Ortiz

9

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8 June 2020

Toshio Heike

10

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8 June 2020

Jordi Yagüe

15

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8 June 2020

Concha Delgado-Beltran

17

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8 June 2020

publication date

6 June 2016

1 reference

17 September 2017

Arthritis & Rheumatology

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27273849%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

volume

68

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8 June 2020

issue

12

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8 June 2020

page(s)

3035-3041

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27273849%20AND%20SRC:MED&resulttype=core&format=json

Phenotypic and genotypic characteristics of cryopyrin-associated periodic syndrome: a series of 136 patients from the Eurofever Registry.

8 June 2020

cites work

1 reference

Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle-Wells syndrome

21 January 2018

1 reference

De novo CIAS1 mutations, cytokine activation, and evidence for genetic heterogeneity in patients with neonatal-onset multisystem inflammatory disease (NOMID): a new member of the expanding family of pyrin-associated autoinflammatory diseases

21 January 2018

1 reference

Chronic infantile neurological cutaneous and articular syndrome is caused by mutations in CIAS1, a gene highly expressed in polymorphonuclear cells and chondrocytes

21 January 2018

1 reference

NALP3 forms an IL-1beta-processing inflammasome with increased activity in Muckle-Wells autoinflammatory disorder

21 January 2018

1 reference

High incidence of NLRP3 somatic mosaicism in patients with chronic infantile neurologic, cutaneous, articular syndrome: results of an International Multicenter Collaborative Study

21 January 2018

1 reference

Somatic NLRP3 mosaicism in Muckle-Wells syndrome. A genetic mechanism shared by different phenotypes of cryopyrin-associated periodic syndromes.

21 January 2018

1 reference

A somatic NLRP3 mutation as a cause of a sporadic case of chronic infantile neurologic, cutaneous, articular syndrome/neonatal-onset multisystem inflammatory disease: Novel evidence of the role of low-level mosaicism as the pathophysiologic mechanis

21 January 2018

1 reference

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

21 January 2018

1 reference

A novel flow cytometric method to assess inflammasome formation

21 January 2018

1 reference

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

21 January 2018

1 reference

A genomic view of mosaicism and human disease

21 January 2018

1 reference

Central tolerance: learning self-control in the thymus

21 January 2018

1 reference

Two-year results from an open-label, multicentre, phase III study evaluating the safety and efficacy of canakinumab in patients with cryopyrin-associated periodic syndrome across different severity phenotypes

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/ART.39770

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27273849%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

1 reference