NOD2-associated pediatric granulomatous arthritis, an expanding phenotype: study of an international registry and a national cohort in Spain. (Q37401815)

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scientific article published on June 2009

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English	NOD2-associated pediatric granulomatous arthritis, an expanding phenotype: study of an international registry and a national cohort in Spain.	scientific article published on June 2009

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scholarly article

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29 January 2020

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

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29 January 2020

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Juan I Arostegui

2

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29 January 2020

13

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29 January 2020

author name string

Carlos D Rosé

1

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29 January 2020

Tammy M Martin

3

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29 January 2020

Graciela Espada

4

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29 January 2020

Lisabeth Scalzi

5

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29 January 2020

Jordi Yagüe

6

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29 January 2020

James T Rosenbaum

7

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29 January 2020

Consuelo Modesto

8

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29 January 2020

Maria Cristina Arnal

9

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29 January 2020

Rosa Merino

10

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29 January 2020

Julia García-Consuegra

11

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29 January 2020

María Antonia Carballo Silva

12

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29 January 2020

publication date

1 June 2009

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29 January 2020

Arthritis and Rheumatism

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29 January 2020

60

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29 January 2020

6

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29 January 2020

1797-1803

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Europe PubMed Central

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29 January 2020

CARD15 mutations in Blau syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2768567

6 September 2017

Renal granulomatous sarcoidosis in childhood: a report of 11 cases and a review of the literature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2768567

6 September 2017

NOD2 gene-associated pediatric granulomatous arthritis: clinical diversity, novel and recurrent mutations, and evidence of clinical improvement with interleukin-1 blockade in a Spanish cohort

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2768567

14 September 2017

Abdominal aortic aneurysm associated with childhood sarcoidosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2768567

14 September 2017

Sarcoidosis of early onset. A challenge for the pediatric rheumatologist.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2768567

28 September 2017

Early onset sarcoidosis with aortitis--"juvenile systemic granulomatosis?".

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2768567

28 September 2017

Familial granulomatous synovitis, uveitis, and cranial neuropathies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2768567

26 June 2018

Blau syndrome mutation of CARD15/NOD2 in sporadic early onset granulomatous arthritis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2768567

2 September 2018

CARD15 mutations in familial granulomatosis syndromes: a study of the original Blau syndrome kindred and other families with large-vessel arteritis and cranial neuropathy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2768567

2 September 2018

Familial Granulomatous Arteritis with Polyarthritis of Juvenile Onset

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2768567

2 September 2018

Familial granulomatous arthritis, iritis, and rash

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2768567

5 November 2018

Early onset sarcoidosis: not a benign disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19479837

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial granulomatous arthritis (Blau syndrome) with granulomatous renal lesions

1 reference

https://pubmed.ncbi.nlm.nih.gov/19479837

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Early-onset sarcoidosis and CARD15 mutations with constitutive nuclear factor-kappaB activation: common genetic etiology with Blau syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/19479837

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pediatric granulomatous arthritis: an international registry

1 reference

https://pubmed.ncbi.nlm.nih.gov/19479837

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interstitial pneumonitis in Blau syndrome with documented mutation in CARD15

1 reference

https://pubmed.ncbi.nlm.nih.gov/19479837

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Granulomatous nephritis associated with R334Q mutation in NOD2

1 reference

https://pubmed.ncbi.nlm.nih.gov/19479837

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular analysis of the MVK and TNFRSF1A genes in patients with a clinical presentation typical of the hyperimmunoglobulinemia D with periodic fever syndrome: a low-penetrance TNFRSF1A variant in a heterozygous MVK carrier possibly influences the

1 reference

https://pubmed.ncbi.nlm.nih.gov/19479837

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sarcoid arthritis in children

1 reference

https://pubmed.ncbi.nlm.nih.gov/19479837

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Vasculopathy with renal artery stenosis in a child with sarcoidosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19479837

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant granulomatous arthritis, uveitis, skin rash, and synovial cysts

1 reference

https://pubmed.ncbi.nlm.nih.gov/19479837

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Liver involvement in familial granulomatous arthritis (Blau syndrome)

1 reference

https://pubmed.ncbi.nlm.nih.gov/19479837

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1002/ART.24533

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Europe PubMed Central

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29 January 2020

PMC publication ID

1 reference

Europe PubMed Central

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29 January 2020

PubMed publication ID

1 reference

Europe PubMed Central

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29 January 2020

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