Results 201 to 210 of about 34,596 (267)

Assessment of Nutritional Status in Children with Familial Mediterranean Fever Using Prognostic Nutritional Index and Controlling Nutritional Status Score: Relationship with Clinical Findings and MEFV Mutations. [PDF]

Children (Basel)
Dogantan S, Keskin A, Bozkaya Yücel B, Perk P, Aytaç Kaplan EH, Koç R, Eren Akarcan S.   +6 more
europepmc   +1 more source

Biochemical and Cell Biological Studies of TRIM37 Defective in Mulibrey Nanism [PDF]

, 2006
Kallijärvi, Jukka
core  

The Turkish Pain Catastrophizing Scale-Child in Adolescents with Familial Mediterranean Fever: A Psychometric Analysis. [PDF]

Arch Rheumatol
Sarac DC, Bayraktar D, Altug Gucenmez O, Bora B, Savci S, Unsal SE.   +5 more
europepmc   +1 more source

Expanding the Spectrum: a case of Giant cell arteritis encountered in familial Mediterranean fever. [PDF]

Oxf Med Case Reports
Moncayo RD, Sultanov MB, Tun MTH, Mohammadrezaei F, Khan OA, Gutierrez D, Konka S.   +6 more
europepmc   +1 more source

Human population of the Balearic Island: the case of Chuetas and Ibizans [PDF]

, 2008
Castro, José A., Picornell, Antònia, Ramon i Juanpere, M. Misericòrdia   +2 more
core  

Familial Mediterranean Fever: An Autoinflammatory Genetic Disorder. [PDF]

Cureus
Lopes Freitas R, Pereira N, Pereira A.
europepmc   +1 more source

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Familial Mediterranean Fever

La Presse Médicale, 2019
Familial Mediterranean Fever (FMF) is the oldest and the most frequent of all described hereditary periodic fever syndromes. The populations originating from Mediterranean basin carry the highest risk for FMF however it is being increasingly recognized in many parts of the world.
Huri, Ozdogan, Serdal, Ugurlu
semanticscholar   +4 more sources

Ancient familial Mediterranean fever mutations in human pyrin and resistance to Yersinia pestis

Nature Immunology, 2020
Familial Mediterranean fever (FMF) is an autoinflammatory disease caused by homozygous or compound heterozygous gain-of-function mutations in MEFV, which encodes pyrin, an inflammasome protein. Heterozygous carrier frequencies for multiple MEFV mutations
Elaine F Remmers, Wonyong Lee, Amanda K Ombrello   +2 more
exaly   +2 more sources

Clinical significance of E148Q heterozygous variant in paediatric Familial Mediterranean Fever.

Rheumatology, 2021
OBJECTIVES Familial Mediterranean Fever (FMF) results from mutations in the Mediterranean fever (MEFV) gene. The p.E148Q is one of the most frequent protein alternations in the MEFV gene, yet the exact E148Q genotype-phenotype correlation remains unclear.
I. Tirosh, Yonatan Yacobi, A. Vivante, O. Barel, Yishay Ben-Moshe, Ortal Erez Granat, S. Spielman, R. Semo Oz, Y. Shinar, M. Gerstein   +9 more
semanticscholar   +1 more source

Familial Mediterranean fever

Current Opinion in Rheumatology, 2016
Purpose of review Familial Mediterranean fever (FMF) is the oldest and most common of the hereditary autoinflammatory diseases (AIDs). A large body of information has been accumulated over recent years on the pathophysiology, diagnosis and treatment of these diseases. The purpose of this review is to bring an up-to-date summary
Shai, Padeh, Yackov, Berkun
openaire   +3 more sources