Results 111 to 120 of about 8,365 (219)

MEFV geninde allelik ifadenin kantitasyonu

, 2020
89
openaire   +1 more source

Associations of MEFV gene variants, IL-33, and sST2 with the risk of Henoch-Schönlein purpura in children

Heliyon
Objective: Henoch-Schönlein purpura (HSP) is the most common systemic vasculitis in children. HSP is a multifactorial inflammatory disease, but its pathogenesis is still unclear.
Yang Ruan, Longlong Xie
doaj   +1 more source

Pyrin dephosphorylation is sufficient to trigger inflammasome activation in familial Mediterranean fever patients

EMBO Molecular Medicine, 2019
Familial Mediterranean fever (FMF) is the most frequent hereditary systemic autoinflammatory syndrome. FMF is usually caused by biallelic mutations in the MEFV gene, encoding Pyrin.
Flora Magnotti, Lucie Lefeuvre, Sarah Benezech, Tiphaine Malsot, Louis Waeckel, Amandine Martin, Sébastien Kerever, Daria Chirita, Marine Desjonqueres, Agnès Duquesne, Mathieu Gerfaud‐Valentin, Audrey Laurent, Pascal Sève, Michel‐Robert Popoff, Thierry Walzer, Alexandre Belot, Yvan Jamilloux, Thomas Henry   +17 more
doaj   +1 more source

Abstracts

Molecular Oncology, Volume 19, Issue S1, Page 1-940, June 2025.
Abstracts submitted to the ‘EACR 2025 Congress: Innovative Cancer Science’, from 16–19 June 2025 and accepted by the Congress Organising Committee are published in this Supplement of Molecular Oncology, an affiliated journal of the European Association for Cancer Research (EACR).
wiley   +1 more source

Coexisting Diseases in Patients with Familial Mediterranean Fever

Open Access Rheumatology: Research and Reviews, 2020
Farhad Salehzadeh,1 Afsaneh Enteshari Moghaddam2 1Pediatric Department, Bouali Children`s Hospital, Ardabil University of Medical Sciences (ARUMS), Ardabil, Iran; 2Internal Medicine Department, Imam Khomeini Hospital, Ardabil University of Medical ...
Salehzadeh F, Enteshari Moghaddam A
doaj  

PFAPA syndrome is not a sporadic disease [PDF]

, 2017
Objectives. To determine whether PFAPA (periodic fever, aphthous stomatitis, pharyngitis and cervical adenitis) patients have a positive family history (FH) for recurrent fever syndromes. Method.
Clet, Johanna, Cochard, Marie, Faouzi, Mohammed, Guéron, Thierry, Hofer, Michaël, Le, Lan, Onrubia, Xavier, Pillet, Pascal   +7 more
core  

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  

Maximal expiratory flow rates in South Indian sportsmen. [PDF]

, 1987
The maximal Expiratory Flow Volume (MEFV) loop is superior to peak expiratory Flow Rate (PFR) and Forced Expiratory Volume in one second (FEV1) in that it describes total information during Forced Vital Capacity (FVC) test.
Kuppurao, K V, Prabhakar, R, Vijayan, V K   +2 more
core  

R202Q Mutation of Mediterranean Fever Gene in Iranian patients with Systemic-onset Juvenile Idiopathic Arthritis

Research in Molecular Medicine, 2014
Background: Systemic-onset Juvenile Idiopathic Arthritis (SoJIA) is an autoinflammatory disease with complex genetic trait starts in children less than 16 years of age with fever and cutaneous rash.
Shirin Farivar, Mahdieh Hasani, Reza Shiari   +2 more
doaj  

Клінічний випадок сімейної середземноморської лихоманки як прояву первинного імунодефіциту в дитини [PDF]

, 2014
Мета — ознайомити лікарів із діагностичними критеріями сімейної Середземноморської лихоманки та описати окремий клінічний випадок. Матеріали та методи: метод генеалогічного аналізу, загальноклінічне, імунологічне та молекулярно генетичне обстеження ...
Дмитрук, Тетяна Василівна, Підвисоцька, Наталія Іванівна, Сорокман, Таміла Василівна   +2 more
core