Cargando…

MEFV gene mutation distrubution in Azerbaijan population

Detalles Bibliográficos
Autores principales:	Berdeli, A, Mukhtarova, G, Oz, A, Musayev, S
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2015
Materias:	Poster Presentation
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4599899/ http://dx.doi.org/10.1186/1546-0096-13-S1-P127

Ejemplares similares

Frequencies of the MEFV Gene Mutations in Azerbaijan
por: Huseynova, LS, et al.
Publicado: (2022)

MEFV mutations in systemic JIA
por: Aktay Ayaz, N, et al.
Publicado: (2008)

Prevalence of MEFV gene mutations in apparently healthy Slovenian and Macedonian population
por: Debeljak, M, et al.
Publicado: (2011)

Genetic analysis of MEFV mutation negative familial Mediterranean fever for non-MEFV mutations is rarely effective
por: Ben-Zvi, I, et al.
Publicado: (2015)

Genotype -phenotype correlation of MEFV mutations in Eastern / Central European population
por: Toplak, N, et al.
Publicado: (2015)

MEFV mutations - therapeutic guides or red herrings?
por: Warrier, K, et al.
Publicado: (2015)

P01-022 – MEFV gene mutations registered to infevers
por: Berdeli, A, et al.
Publicado: (2013)

Turkish DIRA patient with novel IL1RN gene mutation
por: Berdeli, A, et al.
Publicado: (2015)

PReS-FINAL-2209: MEFV gene mutations in central and south-eastern European countries
por: Perko, D, et al.
Publicado: (2013)

A case with febrile attacks and vasculopathy associated with ADA2 and MEFV gene mutations
por: Ozdogan, H, et al.
Publicado: (2015)

Clinical and subclinical features and MEFV mutation distribution in of FMF patients’ siblings
por: Gunduz, Z, et al.
Publicado: (2015)

Sweet's syndrome in a patient with compound heterozygous mutations in the Mediterranean fever gene (MEFV)
por: Michelson, M, et al.
Publicado: (2015)

MEFV mutations in Iranian children with systemic onset juvenile idiopathic arthritis
por: Farivar, Shirin, et al.
Publicado: (2014)

MEFV mutation carriage as possible predisposition factor for the development of Post Pericardiotomy Syndrome (PPS)
por: Dechtman, ID, et al.
Publicado: (2015)

The frequency of MEFV gene variations in Adult-onset Still's disease and Gout
por: Ugurlu, S, et al.
Publicado: (2015)

Impact of MEFV genotype in Caucasian children with periodic fever
por: Federici, Silvia, et al.
Publicado: (2011)

Analysis of the mutations in exon 10 of MEFV gene in patients with premature coronary heart disease in west Azerbaijan province of Iran
por: Bagheri, Morteza, et al.
Publicado: (2018)

MEFV and NLRP3 gene variants in children with pfapa syndrome in slovenia
por: Perko, Daša, et al.
Publicado: (2014)

The clinical spectrum of 94 French patients carrying a single mutated MEFV allele
por: Koné-Paut, I, et al.
Publicado: (2008)

Dutch type periodic fever in a Turkish infant also having MEFV mutation
por: Makay, B, et al.
Publicado: (2008)

Description of a case of daily fever, developmental abnormalities, and a heterozygous M694I MEFV mutation
por: Pinto-Patarroyo, G, et al.
Publicado: (2015)

MEFV gene methylation pattern analysis in familial Mediterranean fever patients with altered expression levels
por: Ulum, YZ Akkaya, et al.
Publicado: (2015)

A heterozygous variant in MEFV in a familial autoinflammatory syndrome with PAPA-like features
por: Jéru, I, et al.
Publicado: (2015)

Epidemiological pattern of deaths caused by traffic accidents in East Azerbaijan, Iran
por: Jafari-Khounigh, Ali, et al.
Publicado: (2019)

The epidemiological aspect of traffic injuries mortality in East Azerbaijan province, Iran
por: Pour Doulati, Saeid, et al.
Publicado: (2019)

Utility evaluation of the services provided in international transportation section of East Azerbaijan Province
por: Mirzakhani, Mohammad
Publicado: (2019)

Epidemiology of the last Wednesday Eve Festival injuries in East Azerbaijan Province, Iran
por: Pour Doulati, Saeid, et al.
Publicado: (2019)

Epidemiology of Road Traffic Mortalities among bus / minibus users in East Azerbaijan, Iran
por: Sadeghi-Bazargani, Homayoun, et al.
Publicado: (2019)

Surveying the genetic factors effect to lack of palmaris longus muscle's tendon and prevalence of absence in the inhabitants of Eastern Azerbaijan
por: Hashemiaghdam, A, et al.
Publicado: (2012)

PReS-FINAL-2205: Vascular risk assesment and MMP-3 gene in FMF
por: Sozeri, B, et al.
Publicado: (2013)

Patient with FMF and Triple MEFV Gene Mutations
por: Salehzadeh, Farhad, et al.
Publicado: (2015)

Repeated Necrotizing Lymphadenitis with MEFV Gene Mutations
por: Yamamura, Yuta, et al.
Publicado: (2021)

Next-Generation Sequencing Analysis of MVK, NLRP3, TNFRSF1A, and PSTPIP1 Genes in Patients without MEFV Gene Variation and Genotype–Phenotype Correlation
por: Vuran, Gamze, et al.
Publicado: (2022)

First report of MEFV duplication in FMF patient
por: Sarrabay, G, et al.
Publicado: (2015)

PW01-003 – Frequency of MEFV mutations in Turkish population
por: Yalcinkaya, F, et al.
Publicado: (2013)

Prediction of More Severe MEFV Gene Mutations in Childhood
por: Güneş-Yılmaz, Seviye, et al.
Publicado: (2021)

MEFV Gene Profile in Northwest of Iran, Twelve Common MEFV Gene Mutations Analysis in 216 Patients with Familial Mediterranean Fever
por: Salehzadeh, Farhad, et al.
Publicado: (2015)

Colchicine trial in PFAPA Syndrome and MEFV-negative patients
por: Kadhim, C, et al.
Publicado: (2015)

Common Mediterranean Fever (MEFV) Gene Mutations Associated with Ankylosing Spondylitis in Turkish Population
por: Yigit, Serbulent, et al.
Publicado: (2012)

Autoinflammation due to homozygous S208 MEFV mutation
por: Hong, Ying, et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_2vmengqviokj4p2mrin22k4e5n