Results 11 to 20 of about 30,113 (242)

FMF revisited [PDF]

open access: yesEuropean Journal of Human Genetics, 2004
n ...
Manna, Raffaele   +4 more
openaire   +2 more sources

P01-043 – Comparative characteristic of FMF and FMF with HSP [PDF]

open access: yesPediatric Rheumatology, 2013
According the literature data about Familial Mediterranean Fever (FMF), with the combination of Henoch- Sheilen purpura (HSP), as well as the results of the work done by the former of our studies we attempt to identify and compare membranes aspects of pathogeneses of FMF and combination of FMF with HSP.
Sargsyan, H, Ghazaryan, P
openaire   +1 more source

FMF: an update [PDF]

open access: yesPediatric Rheumatology, 2014
Familial Mediterranean fever (FMF) is the most common autoinflammatory disease over the world. This autosomal recessively inherited disease is due to mutations in the gene coding for pyrin. Disease causing mutations in the gene are associated with excessive levels of IL-1.
openaire   +2 more sources

Dimensional crossover of the fundamental-measure functional for parallel hard cubes [PDF]

open access: yes, 1997
We present a regularization of the recently proposed fundamental-measure functional for a mixture of parallel hard cubes. The regularized functional is shown to have right dimensional crossovers to any smaller dimension, thus allowing to use it to study ...
A. González   +16 more
core   +3 more sources

Screening for Fabry’s disease in a high-risk subpopulation of FMF

open access: yesEuropean Journal of Medical Research, 2022
Background Familial Mediterranean fever (FMF) is an autosomal recessive disease associated with mutations in the Mediterranean fever gene (MEFV) that manifests with recurrent episodes of febrile serositis.
Tomer Maller   +3 more
doaj   +1 more source

Monogenic auto-inflammatory diseases in children and adults: what a rheumatologist should know

open access: yesНаучно-практическая ревматология, 2019
The article presents information on the current state of the problem of autoinflammatory diseases (AID) in rheumatology, reflects the clinical and demographic, laboratory and molecular genetic characteristics of the main monogenic AID (mAID), the most ...
S. O. Salugina   +2 more
doaj   +1 more source

Comparison of Familial Mediterranean Fever patients by triglyceride/high-density lipoprotein ratio

open access: yesAdıyaman Üniversitesi Sağlık Bilimleri Dergisi, 2021
Aim: In this study, we aimed to show whether there is a relationship between FMF disease and cardiovascular risk by comparing Triglyceride/HDL-Cholesterol ratios between FMF patients and the control group.Materials and Methods: A total of 300 patients ...
Ahmet Aktaş   +2 more
doaj   +1 more source

Serum Calprotectin in Children with Familial Mediterranean Fever [PDF]

open access: yesPediatric Sciences Journal
Background: Familial Mediterranean fever (FMF) is the most prevalent inherited autoinflammatory disease worldwide. Ongoing subclinical inflammation, induces amyloidosis, even during the attack-free periods despite colchicine therapy.
Huda Marzouk   +3 more
doaj   +1 more source

Fuzzy qualitative simulation with multivariate constraints [PDF]

open access: yes, 2014
Postprin
Coghill, George M, Pang, Wei
core   +1 more source

P01-013 – Cochlear involvement in FMF [PDF]

open access: yesPediatric Rheumatology, 2013
FMF is a monogenic autoinflammatory disease with recurring episodes of fever and serositis attacks. FMF is associated with mutations in pyrin. On the other hand mutations in a molecule in the same pathway, cryopyrin, is characterized by inflammatory features involving the inner ear as well.
Ayaz, N Aktay   +8 more
openaire   +2 more sources

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