Results 181 to 190 of about 846,391 (207)

[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

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., Visser, H., Veenstra, J., Baas, F., Siegert, C.E.H.   +4 more
openaire   +2 more sources

Ethnic Distribution and Amyioidosis in Familial Mediterranean Fever (FMF)

Pathologia et Microbiologia, 2010
H, HELLER, E, SOHAR, M, PRAS
openaire   +2 more sources

Trends in colchicine treatment in Familial Mediterranean fever (FMF)

2008
[No abstract available]
La Regina, M., Livneh, A., Manna, R., Ozdogan, H.   +3 more
openaire   +1 more source

Y688X, the first nonsense mutation in familial Mediterranean fever (FMF)

Human Mutation, 2000
C, Notarnicola, R, Manna, J M, Rey, I, Touitou   +3 more
openaire   +2 more sources

Development and validation of a quality of life scale in Familial Mediterranean Fever (FMFQoL)

Modern Rheumatology, 2021
Çagri Unal-Ulutatar, Mehmet Tuncay Duruoz   +1 more
exaly  

Mediterranean Fever, Familial (FMF)

2008
openaire   +1 more source

Successful treatment with anti-tumor necrosis factor (anti-TNF)-alpha of proteinuria in a patient with familial mediterranean fever (FMF) resistant to colchicine: anti-TNF drugs and FMF

Rheumatology International, 2011
S Erten
exaly  

Incidence of familial Mediterranean fever (FMF) mutations among children of Mediterranean extraction with functional abdominal pain

Journal of Pediatrics, 2001
Raanan Shamir, Marwan Shinawi, Ruth Gershoni-Baruch   +2 more
exaly  

[Genetic diagnosis of periodic diseases (familial mediterranean fever or FMF)].

Pathologie-biologie, 2002
Periodic disease is the prototype of a group of hereditary disorders characterised by recurrent inflammatory attacks. Since the discovery of the causing gene (MEFV) in 1997, three hospital laboratories in France, and around 20 throughout the world, propose a specific genetic test, based on the search of the common MEFV mutations on DNA extracted from a
openaire   +1 more source