Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Farhad Salehzadeh"'
Autor:
Kosar Asna Ashari, Nima Parvaneh, Kayvan Mirnia, Mehri Ayati, Maryam Saeedi, Farhad Salehzadeh, Mohammad Shahrooei, Razieh Sangsari, Pejman Rohani, Vahid Ziaee
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 22, Iss 1, Pp 1-7 (2024)
Abstract Background Gain of function (GOF) mutations in NOD-like receptor family CARD-containing 4 protein (NLRC4) gene induce a wide spectrum of autoinflammatory phenotypes. Currently, we categorize them into four groups: familial cold autoinflammat
Externí odkaz:
https://doaj.org/article/028afa411aba48dba285ddbd43f4f0f5
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 22, Iss 1, Pp 1-5 (2024)
Abstract Background Juvenile idiopathic recurrent parotitis (JIRP) in children is a condition characterized with recurrent episodes of idiopathic parotid gland inflammation. Since there are no definitive guidelines for diagnosis and management of thi
Externí odkaz:
https://doaj.org/article/a663dc3486d14fa796d67ec1689638c5
Autor:
Farhad Salehzadeh
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 22, Iss 1, Pp 1-3 (2024)
Externí odkaz:
https://doaj.org/article/29c1da597fc540909ef96f8087ec8b2a
Autor:
Farhad Salehzadeh, Farhad Pourfarzi, Rasool Molatefi, Behzad Davarnia, Ehsan Shahbazfar, Farzad Ahmadabadi
Publikováno v:
Iranian Journal of Medical Sciences, Vol 48, Iss 1, Pp 43-48 (2023)
Background: In December 2019, an outbreak of pneumonia caused by the novel coronavirus disease 2019 (COVID-19) became a pandemic and caused a global health crisis. This study evaluates the immunogenic potential of the Mediterranean fever (MEFV) gene
Externí odkaz:
https://doaj.org/article/5a1c109d6f6849b18216ea22e7fcf728
Publikováno v:
Jorjani Biomedicine Journal, Vol 10, Iss 3, Pp 7-14 (2022)
Background and objectives: Behcet's Disease (BD) is a rare severe recurrent inflammatory disorder affecting several body organs. Since Familial Mediterranean Fever (FMF) and BD affect almost a specific population, both diseases can mimic the other cl
Externí odkaz:
https://doaj.org/article/288052bf72e44960af64790e2710d30e
Autor:
Farhad Salehzadeh, Mehrdad Mirzarahimi
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 18, Iss 1, Pp 1-4 (2020)
Abstract Background Recurrent and relapsing arthritis has been proposed to describe a group of arthritis with recurring and periodic nature, in which the joints are intermittently involved. This study reports three non-FMF patients with heterozygous
Externí odkaz:
https://doaj.org/article/be9e26eeb1f04d6c8c8d90c18058712c
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 17, Iss 1, Pp 1-4 (2019)
Abstract Background Relapsing periodic arthritis is a general term used for a group of diseases with recurring and periodic nature, in which the joints are intermittently involved. The aim of this study is to evaluation of the possible relationship b
Externí odkaz:
https://doaj.org/article/26a388b9a17341fab20cb46d8c3fd6a5
Autor:
Farhad Salehzadeh, Afshan Sharghi, Atena Moteyagheni, Saeid Hosseini asl, Mahsa Mottaghi, Sepehr Sarkhanloo
Publikováno v:
Journal of Ardabil University of Medical Sciences, Vol 19, Iss 1, Pp 110-116 (2019)
Background & objectives: MEFV gene has a major role in Familial Mediterranean Fever (FMF) as an auto-inflammatory disorder. FMF is most often seen in the people of the Mediterranean area. Considering the significant role of the MEFV gene in many rheu
Externí odkaz:
https://doaj.org/article/f2a3ae4310934f76b2a14021f24e2eaf
Publikováno v:
Clinical Medicine Insights: Case Reports, Vol 12 (2019)
Background: Chronic infantile neurologic cutaneous and articular syndrome (CINCA) is the most severe phenotype of cryopyrin-associated periodic syndromes (CAPS) and is caused by a missense mutation in NLRP3 gene. Case presentation: We are reporting a
Externí odkaz:
https://doaj.org/article/516d06cd95144a3e8dde7c7f8208ae08
Publikováno v:
Case Reports in Rheumatology, Vol 2019 (2019)
Background and Objective. CRMO is an inflammatory disease of bone that occurs more often in children. The clinical manifestations are intermittent fever, pain, and bone lesions, especially in long bones. Although there is an idiopathic type of diseas
Externí odkaz:
https://doaj.org/article/a17bb437ce1a4b9586ccc6568b67236a