Familial mediterranean fever fmf

Results 191 to 200 of about 7,121 (223)

Some of the next articles are maybe not open access.

[Amyloidosis of familial Mediterranean fever (FMF)--insights to FMF phenotype II].

Harefuah, 2007
Amyloidosis is the most grievous manifestation of Familial Mediterranean Fever (FMF), occurring in a high proportion of untreated patients. Continuously elevated serum amyloid A (SAA) levels during remissions, rather than a pulsatile rise during FMF attacks, underlies the development of amyloidosis.
openaire +1 more source

The arthritis of familial mediterranean fever (FMF)

Arthritis & Rheumatism, 1966
H, Heller +7 more
openaire +2 more sources

Familial Mediterranean Fever (FMF): a single centre retrospective study in Amsterdam.

The Netherlands journal of medicine, 2019
Familial Mediterranean Fever (FMF) is the earliest described and most prevalent hereditary auto-inflammatory disease. Its clinical presentation is diverse, leading to possible delay in diagnosis and treatment. Due to immigration, FMF became common in non-Mediterranean European regions.
Hageman, I.M.G. +4 more
openaire +2 more sources

Climate Change and Weather Extremes in the Eastern Mediterranean and Middle East

Reviews of Geophysics, 2022
George Zittis, , Pinhas Alpert
exaly

PATH TO DIAGNOSIS IN FAMILIAL MEDITERRANEAN FEVER (FMF)

[No abstract available]
Karup, Sejla +6 more
openaire +2 more sources

The gut microbiome modulates the protective association between a Mediterranean diet and cardiometabolic disease risk

Nature Medicine, 2021
Dong D Wang, Long H Nguyen, Yanping Li
exaly

MEFV gene mutation spectrum in familial Mediterranean fever (FMF)