Results 81 to 90 of about 3,177,015 (166)

Detection and characterization of rickettsiae in Western Australia [PDF]

, 2007
The aim of this study was to address the shortfall in current, in-depth knowledge of Western Australian rickettsiae investigating in particular, the role of native and feral animals as reservoir hosts.
Owen, Helen Clare
core  

Genotyping of familial Mediterranean fever gene (MEFV)-Single nucleotide polymorphism-Comparison of Nanopore with conventional Sanger sequencing. [PDF]

PLoS One, 2022
Schmidt J, Berghaus S, Blessing F, Herbeck H, Blessing J, Schierack P, Rödiger S, Roggenbuck D, Wenzel F.   +8 more
europepmc   +1 more source

Mediterranean fever gene variants modify clinical phenotypes of idiopathic multi-centric Castleman disease. [PDF]

Clin Exp Immunol, 2021
Endo Y, Koga T, Ubara Y, Sumiyoshi R, Furukawa K, Kawakami A.   +5 more
europepmc   +1 more source

A rare cause of fever in an adult: a case of familial Mediterranean fever

, 2018
Ilknur Erdem,1 Fatih Saritas,2 Ritvan Karaali,1 Enes Ardic,1 Gaye Kubra Emeksiz,3 Sonat Pinar Kara,3 R Merve Yaniker,4 Oguzhan Bol4 1Department of Infectious Diseases, Faculty of Medicine, Namik Kemal University, Tekirdag, Turkey; 2Clinic of Rheumatology,
Saritas F, Emeksiz GK, Kara SP, Yaniker RM, Bol O, Ardic E, Erdem I, Karaali R   +7 more
core  

Familial Mediterranean fever [PDF]

, 2004
peer reviewedFamilial Mediterranean Fever (FMF) is an hereditary disease that especially affects people living around the Mediterranean sea. It is characterized by recurring fever and abdominal pain, eventually associated with localised
Hermesse, A., Leclercq, P., Malaise, Michel   +2 more
core   +1 more source

MEFV Gene Mutations in Behçet’s Disease

Eurasian Journal of Medicine, 2019
Behçet's disease is a chronic inflammatory multisystemic disorder of unknown cause, characterized by orogenital ulcers, uveitis, skin lesions, vascular, locomotor, pulmoner, gastrointestinal, and central nervous system manifestations.
Fazile Hatipoğlu Erdem
doaj  

Association between sequence variations of the Mediterranean fever gene and the risk of migraine: a case–control study

Neuropsychiatric Disease and Treatment, 2016
Salih Coşkun,1 Sefer Varol,2 Hasan H Özdemir,2 Sercan Bulut Çelik,3 Metin Balduz,4 Mehmet Akif Camkurt,5 Abdullah Çim,1 Demet Arslan,2 Mehmet Uğur Çevik2 1Department of Medical Genetics, 2Department of Neurology,
Coskun S, Varol S, Ozdemir HH, Bulut Celik S, Balduz M, camkurt MA, Cim A, Arslan D, Cevik MU   +8 more
doaj  

Clinical report of Mediterranean fever in a child in Ukraine – Don’t miss it!

Сучасна педіатрія: Україна
Introduction. Familial Mediterranean fever (FMF) is a non-infectious genetic disease caused by a mutation in the MEFV gene. This disease is more common in people of Mediterranean or Middle Eastern descent, but can occur in any ethnic group, including ...
К.Y. Pashenko, Т.V. Frolova, Y.V. Кarpushenko, G.R. Muratov, О.М. Savvo, Т.О. Khalturina, О.М. Ashcheulov   +6 more
doaj   +1 more source

A Unique Complex Variation Profile in a Patient with Familial Mediterranean Fever (FMF): Triple Homozygous E148Q-P369S-R408Q – “Case Report”

The Application of Clinical Genetics
Nour Abi Chakra,1,* Nadine Yazbeck,2,* Mohammad Omar Fattah,3 Rima Hanna-Wakim2,4,5 1American University of Beirut, Beirut, Lebanon; 2Department of Pediatrics and Adolescent Medicine, American University of Beirut, Beirut, Lebanon ...
Abi Chakra N, Yazbeck N, Fattah MO, Hanna-Wakim R   +3 more
doaj  

Vasculitis and long standing ankylosing spondylitis in a patient with familial Mediterranean fever

Journal of Research in Medical Sciences, 2014
Coexistence of familial Mediterranean fever (FMF) and other inflammatory disorders has been frequently reported, but no specific underlying factor has been identified.
Ali Taylan, Yasar Yildiz, Ismail Sari, Guliz Ozkok   +3 more
doaj