Zobrazeno 1 - 10
of 65
pro vyhledávání: '"Keivan Basiri"'
Autor:
Reza Boostani, Nahid Olfati, Hosein Shamshiri, Zanireh Salimi, Farzad Fatehi, Seyed Arya Hedjazi, Atefeh Fakharian, Majid Ghasemi, Ali Asghar Okhovat, Keivan Basiri, Bahram Haghi Ashtiani, Behnaz Ansari, Gholam Reza Raissi, Seyed Ahmadreza Khatoonabadi, Payam Sarraf, Sara Movahed, Akram Panahi, Bentolhoda Ziaadini, Mohammad Yazdchi, Jalal Bakhtiyari, Shahriar Nafissi
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
Amyotrophic lateral sclerosis (ALS) is a rapidly progressive neurodegeneration involving motor neurons. The 3–5 years that patients have to live is marked by day-to-day loss of motor and sometimes cognitive abilities. Enormous amounts of healthcare
Externí odkaz:
https://doaj.org/article/e73a460674ad45b1a4c8e46fcd5c0acf
Autor:
Hamidreza Mianesaz, Safoura Ghalamkari, Mansoor Salehi, Mahdiyeh Behnam, Majid Hosseinzadeh, Keivan Basiri, Majid Ghasemi, Maryam Sedghi, Behnaz Ansari
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 2, Pp n/a-n/a (2023)
Abstract Background Limb‐girdle muscular dystrophy (LGMD) is a non‐syndromic muscular dystrophy caused by variations in the genes involved in muscle structure, function and repair. The heterogeneity in the severity, progression, age of onset, and
Externí odkaz:
https://doaj.org/article/d474172c545b4bdaa3846f360e4c73ba
Autor:
Narges Karimi, Reza Boostani, Farzad Fatehi, Akram Panahi, Ali Asghar Okhovat, Bentolhoda Ziaadini, Keivan Basiri, Siamak Abdi, Farnaz Sinaei, Mojtaba Rezaei, Gholamreza Shamsaei, Behnaz Ansari, Shahriar Nafissi
Publikováno v:
Basic and Clinical Neuroscience, Vol 12, Iss 5, Pp 703-710 (2021)
Introduction: Guillain-Barre Syndrome (GBS) is an autoimmune acute inflammatory demyelinating polyneuropathy usually elicited by an upper respiratory tract infection. Several studies reported GBS associated with Coronavirus Disease 2019 (COVID-19) in
Externí odkaz:
https://doaj.org/article/89bc8cc928c649e6bdf18730add931fb
Autor:
Keivan Basiri, Behnaz Ansari
Publikováno v:
Acta Medica Iranica, Vol 59, Iss 1 (2021)
The reason why the experiments were done: previous studies have shown that the incidence rates vary in different populations. Now we report the preliminary results of the screening study. Pompe disease is a rare but potentially treatable disorder cau
Externí odkaz:
https://doaj.org/article/1fda128d0cc14ec08a327165dd3c4c7d
Publikováno v:
مجله دانشکده پزشکی اصفهان, Vol 34, Iss 370, Pp 41-48 (2016)
Background: Median neuropathy due to nerve compression in the wrist, or carpal tunnel syndrome (CTS), is the most common entrapment neuropathy. Incidence of CTS is high at an estimated value of 280.6 per 100,000 patients per year. Accurate diagnosis
Externí odkaz:
https://doaj.org/article/66bb8dc49ac342f894117e009e22ab60
Publikováno v:
Journal of Research in Medical Sciences, Vol 19, Iss 2, Pp 106-111 (2014)
Background: Considering the dramatic increasing rate of diabetes and consequently its related complications, most importantly diabetic peripheral neuropathy (DPN), challenges regarding proper treatment of DPN and its effect on the quality-of-life and
Externí odkaz:
https://doaj.org/article/677f152ea5e642d4b25c4125765d1f03
Publikováno v:
Journal of Research in Medical Sciences, Vol 18, Iss 5, Pp 438-441 (2013)
Various forms of neuropathy are seen diabetic patients; chronic inflammatory demyelinating polyneuropathy (CIDP) seems not to be infrequent neuropathy in patients suffering from diabetes and it seems to be more common than in the general population;
Externí odkaz:
https://doaj.org/article/05a9317467da4c4aacb8bae044a4119f
Autor:
Rokhsareh Meamar, Leila Dehghani, Majid Ghasemi, Mohamad Saadatnia, Keivan Basiri, Nazanin Alaei Faradonbeh, Shaghayegh Haghjooy Javanmard
Publikováno v:
Journal of Research in Medical Sciences, Vol 18, Iss 13, Pp 1-5 (2013)
Background: Alzheimer′s disease (AD) is a progressive neurodegenerative disease in which endothelial cell (EC) can be affected. In brain, functional changes in ECs contribute to reductions in resting blood flow. Furthermore, angiotensin-converting
Externí odkaz:
https://doaj.org/article/c396ed7efc0548a3881177e63c1a6534
Autor:
Amir Hadi Maghzi, Zahra Fatehi, Vahid Shaygannejad, Fereshteh Ashtari, Fatemeh Derakhshan, Masood Etemadifar, Keivan Basiri, Farzad Fatehi
Publikováno v:
Acta Medica Iranica, Vol 50, Iss 2, Pp 97-100 (2012)
Introduction: None of the approved immunomodulatory drugs in adults Multiple Sclerosis (MS) patients have been officially approved for the pediatric patients and are currently used off-label in this population. Objectives: In this study, we evaluated
Externí odkaz:
https://doaj.org/article/5819526eedf24916b9c2aad0ccd75692
Publikováno v:
Journal of Research in Medical Sciences, Vol 19, Iss 8, Pp 792-794 (2014)
Hereditary inclusion body myopathy (hIBM) is an adult-onset hereditary myopathy, usually with distal onset and quadriceps sparing. This myopathy is autosomal recessive and associated to UPD-N-acetylglucosamine-2-epimerase/N-acetylmannosamine kinase (
Externí odkaz:
https://doaj.org/article/1acc2dfd05e84993b8d5fcca99cff787