(Q24623012)

1

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Valerie Delague

object named as

Valérie Delague

2

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author name string

Eliane Chouery

3

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Nabiha Salem

4

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Mohammed Rawashdeh

5

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Gérard Lefranc

6

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Jacques Loiselet

https://scigraph.springernature.com/pub.10.1186/1471-2350-5-4

7

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language of work or name

English

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publication date

10 February 2004

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published in

BMC Medical Genetics

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volume

5

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page(s)

4

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issue

1

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exact match

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cites work

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The contribution of genotypes at the MEFV and SAA1 loci to amyloidosis and disease severity in patients with familial Mediterranean fever

7 April 2017

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The MICA region determines the first modifier locus in familial Mediterranean fever

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Familial Mediterranean fever in Lebanon: mutation spectrum, evidence for cases in Maronites, Greek orthodoxes, Greek catholics, Syriacs and Chiites and for an association between amyloidosis and M694V and M694I mutations.

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Amyloidosis induced, end stage renal disease in patients with familial Mediterranean fever is highly associated with point mutations in the MEFV gene

27 September 2017

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Identification of MEFV-independent modifying genetic factors for familial Mediterranean fever

27 September 2017

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MEFV-Gene analysis in armenian patients with Familial Mediterranean fever: diagnostic value and unfavorable renal prognosis of the M694V homozygous genotype-genetic and therapeutic implications

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Triplet repeat polymorphism in the transmembrane region of the MICA gene: a strong association of six GCT repetitions with Behçet disease

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

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Systemic amyloidosis and the gastrointestinal tract

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Influence of genotypes at SAA1 and SAA2 loci on the development and the length of latent period of secondary AA-amyloidosis in patients with rheumatoid arthritis

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SAA1 alleles as risk factors in reactive systemic AA amyloidosis

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The MICA-A9 triplet repeat polymorphism in the transmembrane region confers additional susceptibility to the development of psoriatic arthritis and is independent of the association of Cw*0602 in psoriasis

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