(Q40369623)

19 September 2017

title

An infant with severe refractory Crohn's disease and homozygous MEFV mutation who dramatically responded to colchicine (English)

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19 September 2017

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Zarife Kuloğlu

1

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19 September 2017

Aydan Kansu

2

1 reference

19 September 2017

Gonca Ustündağ

3

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19 September 2017

Z Birsin Özçakar

4

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19 September 2017

Arzu Ensari

5

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19 September 2017

Mesiha Ekim

6

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19 September 2017

publication date

5 January 2010

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Rheumatology International

19 September 2017

published in

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19 September 2017

volume

32

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19 September 2017

issue

3

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19 September 2017

page(s)

783-785

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Children with early-onset inflammatory bowel disease (IBD): analysis of a pediatric IBD consortium registry.

19 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS00296-009-1326-4

Crohn disease in patients with familial Mediterranean fever

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00296-009-1326-4

The familial Mediterranean fever (MEVF) gene as a modifier of Crohn's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00296-009-1326-4

Increased frequency of mutations in the gene responsible for familial Mediterranean fever (MEFV) in a cohort of patients with ulcerative colitis: evidence for a potential disease-modifying effect?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00296-009-1326-4

A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00296-009-1326-4

Nod2, a Nod1/Apaf-1 family member that is restricted to monocytes and activates NF-kappaB

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00296-009-1326-4

The immunological and genetic basis of inflammatory bowel disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00296-009-1326-4

A common pathway in periodic fever syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00296-009-1326-4

Interaction between pyrin and the apoptotic speck protein (ASC) modulates ASC-induced apoptosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00296-009-1326-4

Behçet's disease in Familial Mediterranean fever: characterization of the association between the two diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00296-009-1326-4

Prevalence and significance of mutations in the familial Mediterranean fever gene in Henoch-Schönlein purpura

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00296-009-1326-4

Familial Mediterranean fever gene (MEFV) mutations in patients with rheumatic heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00296-009-1326-4

Prevalence and significance of mutations in the familial Mediterranean fever gene in patients with Crohn's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00296-009-1326-4

The familial Mediterranean fever (MEFV) gene may be a modifier factor of inflammatory bowel disease in infancy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00296-009-1326-4

Inflammatory bowel disease in non-Ashkenazi Jews with familial Mediterranean fever

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20049453

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S00296-009-1326-4

1 reference

Dimensions Publication ID

19 September 2017

1037868346

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