Results 191 to 200 of about 30,113 (242)

Prenatal Screening for Monosomy X in the First Trimester: A Comparison of a Thai Predictive Model and the Fetal Medicine Foundation Algorithm. [PDF]

Int J Womens Health
Kongsung N, Tongprasert F, Kunanukulwatana C, Tongsong T.   +3 more
europepmc   +1 more source

A Case of Familial Mediterranean Fever Diagnosed After Oral Administration of a Gonadotropin-Releasing Hormone (GnRH) Antagonist. [PDF]

Cureus
Ueno H, Ohara R, Nakao S, Sasaki J, Satoh T.   +4 more
europepmc   +1 more source

Familial Mediterranean Fever: A Diagnostic and Therapeutic Challenge. [PDF]

Cureus
Sia R.
europepmc   +1 more source

[Familial Mediterranean fever (FMF)].

Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion, 1998
openaire   +1 more source

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Association of FMF-Related (MEFV) Point Mutations with Secondary and FMF Amyloidosis

Nephron Clinical Practice, 2004
<i>Background:</i> Familial Mediterranean fever (FMF) is the major cause of AA amyloidosis in Turkey. M694V mutation in MEFV gene was suggested to be associated with severe clinical features and amyloidosis of FMF. <i>Methods:</i> In this study, the frequencies of three FMF-related MEFV mutations (M694V, M680I and V726A) were ...
M Pamir, Atagunduz, Serhan, Tuglular, Gulcin, Kantarci, Emel, Akoglu, Haner, Direskeneli   +4 more
openaire   +3 more sources

Polyarteritis nodosa in patients with Familial Mediterranean Fever (FMF): A concomitant disease or a feature of FMF?

Seminars in Arthritis and Rheumatism, 2001
Familial Mediterranean Fever (FMF) is caused by mutations in the gene encoding pyrin and is characterized by self-limited, recurrent attacks of fever and serositis. Vasculitis has been increasingly reported in FMF. A study evaluating the prognosis in FMF and polyarteritis nodosa (PAN) patients has not been reported previously.To determine the special ...
S, Ozen, E, Ben-Chetrit, A, Bakkaloglu, H, Gur, K, Tinaztepe, M, Calguneri, C, Turgan, A, Turkmen, I, Akpolat, M, Danaci, N, Besbas, T, Akpolat   +11 more
openaire   +2 more sources

The spectrum of Familial Mediterranean Fever (FMF) mutations [PDF]

European Journal of Human Genetics, 2001
Familial Mediterranean Fever (FMF) is the prototype of a group of inherited inflammatory disorders. The gene (MEFV) responsible for this disease, comprises 10 exons and 781 codons. Twenty-nine mutations, most located in the last exon, have been identified so far. It is unclear whether all are true disease-causing mutations.
Isabelle Touitou
exaly   +3 more sources

Epidemiology of FMF Worldwide

2015
The familial Mediterranean fever (FMF) is the primarily described and most prevalent autoinflammatory disease known in the world. FMF was so named by Heller, because of its high prevalence in the Mediterranean population [1]. Indeed, it was previously denominated as benign paroxysmal peritonitis by Siegal, a New York allergist of Jewish origin [2 ...
Verrecchia, Elena, Sicignano, Ludovico Luca, Cerrito, Lucia, Manna, Raffaele   +3 more
openaire   +2 more sources