Two German CINCA (NOMID) patients with different clinical severity and response to anti-inflammatory treatment (Q40551844)

21 September 2017

Two German CINCA (NOMID) patients with different clinical severity and response to anti-inflammatory treatment (English)

1 reference

21 September 2017

1

Angela Rösen-Wolff

1 reference

21 September 2017

6

Joachim Roesler

1 reference

21 September 2017

5

Manfred Gahr

1 reference

21 September 2017

Jürgen Quietzsch

2

1 reference

PubMed ID

12930324

21 September 2017

Heinz Schröder

series ordinal

3

1 reference

PubMed ID

12930324

21 September 2017

Romy Lehmann

series ordinal

4

1 reference

21 September 2017

1 September 2003

1 reference

European Journal of Haematology

21 September 2017

1 reference

21 September 2017

71

1 reference

21 September 2017

3

1 reference

21 September 2017

215-219

1 reference

TNFRSF1A mutations and autoinflammatory syndromes

21 September 2017

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0609.2003.00109.X

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

https://api.crossref.org/works/10.1034%2FJ.1600-0609.2003.00109.X

Mutations in MVK, encoding mevalonate kinase, cause hyperimmunoglobulinaemia D and periodic fever syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0609.2003.00109.X

Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome. International Hyper-IgD Study Group.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0609.2003.00109.X

Hereditary periodic fever

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0609.2003.00109.X

Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0609.2003.00109.X

Association of mutations in the NALP3/CIAS1/PYPAF1 gene with a broad phenotype including recurrent fever, cold sensitivity, sensorineural deafness, and AA amyloidosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0609.2003.00109.X

New mutations of CIAS1 that are responsible for Muckle-Wells syndrome and familial cold urticaria: a novel mutation underlies both syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0609.2003.00109.X

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

https://api.crossref.org/works/10.1034%2FJ.1600-0609.2003.00109.X

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

https://api.crossref.org/works/10.1034%2FJ.1600-0609.2003.00109.X

The human gene mutation database

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0609.2003.00109.X

A fever gene comes in from the cold

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0609.2003.00109.X

[Chronic, infantile, neurologic, cutaneous and articular syndrome (CINCA) in an infant]

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0609.2003.00109.X

Ancient Missense Mutations in a New Member of the RoRet Gene Family Are Likely to Cause Familial Mediterranean Fever

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0609.2003.00109.X

7 January 2021

A candidate gene for familial Mediterranean fever

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0609.2003.00109.X

7 January 2021

Arthropathy with rash, chronic meningitis, eye lesions, and mental retardation

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0609.2003.00109.X

7 January 2021

Neonatal onset multisystem inflammatory disease

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0609.2003.00109.X

7 January 2021

NOMID--a neonatal syndrome of multisystem inflammation

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0609.2003.00109.X

7 January 2021

10.1034/J.1600-0609.2003.00109.X

Identifiers

DOI

1 reference

21 September 2017

1 reference

PubMed ID

12930324