Zobrazeno 1 - 10
of 64
pro vyhledávání: '"Ariane Sadr Nabavi"'
Autor:
Mohammad Reza Seyyed taghia, Reza Jafarzadeh Esfehani, Reza Boostani, Mohammad Shariati, Ariane Sadr Nabavi
Publikováno v:
Reviews in Clinical Medicine, Vol 8, Iss 1, Pp 35-40 (2021)
Facioscapulohumeral muscular dystrophy is one of the most common musculoskeletal diseases with a considerable burden. Most of the affected individuals experience muscle weakness as the common muscular symptom. Despite the underlying genetic mechanism
Externí odkaz:
https://doaj.org/article/b0b7d3ffcea44b93a4ff20fab5d46689
Autor:
Najmeh Ghatei, Ariane Sadr Nabavi, Mohammad Hossein Bahreyni Toosi, Hosein Azimian, Mansour Homayoun, Reza Ghasemnezhad Targhi, Hossein Haghir
Publikováno v:
Iranian Journal of Basic Medical Sciences, Vol 20, Iss 9, Pp 1037-1041 (2017)
Objective(s): The increasing rate of over using cell phones has been considerable in youths and pregnant women. We examined the effect of mobile phones radiation on genes expression variation on cerebellum of BALB/c mice before and after of the birth
Externí odkaz:
https://doaj.org/article/f03e9b5f82d44e73a7b7dfea4e8d9f12
Autor:
Mohammad Shariati, Alireza Davoudi, Reza Boostani, Farah Ashrafzadeh, Mehran Beiraghi Toosi, Nafiseh Todarbary, Javad Akhondian, Narges Hashemi, Ariane Sadr-Nabavi
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 25, Iss 1, Pp 1-9 (2024)
Abstract Background Spinal muscular atrophy (SMA) is a group of motor neuron diseases. In 95% of SMA patients, the telomeric copy of the SMN gene (SMN1) is homozygously deleted. Due to the autosomal recessive pattern of SMA inheritance, individuals w
Externí odkaz:
https://doaj.org/article/9726dff5249c4ddba995677341c249bf
Autor:
Mohammad Reza Seyedtaghia, Mohammad Soudyab, Mohammad Shariati, Reza Jafarzadeh Esfehani, Shabnam Vafadar, Neda Shalaei, Vahid Nouri, Michael Zech, Julianne Winkelmann, Ali shoeibi, Ariane Sadr-Nabavi
Publikováno v:
Heliyon, Vol 9, Iss 4, Pp e15393- (2023)
Parkinson's disease (PD), a neurodegenerative disease characterized by both motor neuron and non-motor neuron symptoms, is the most frequent neurodegenerative disease after Alzheimer's disease. Both genetic and environmental factors take part in dise
Externí odkaz:
https://doaj.org/article/31a4b48ae4a1462ea37dd4e5ecf297b4
Autor:
Mohammad, Soudyab, Mohammad, Shariati, Reza Jafarzadeh, Esfehani, Neda, Shalaei, Shabnam, Vafadar, Vahid, Nouri, Michael, Zech, Julianne, Winkelmann, Ali, Shoeibi, Ariane, Sadr-Nabavi
Publikováno v:
Journal of Molecular Neuroscience. 72:2486-2496
Parkinson's disease (PD) is a common progressive neurodegenerative disorder with motor and nonmotor symptoms. Recent studies demonstrate various susceptibility loci and candidate genes for familial forms of the disease. However, the genetic basis of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d538c15e8a88bd9f4230bc5b88844d03
https://doi.org/10.1007/s12031-022-02085-9
https://doi.org/10.1007/s12031-022-02085-9
Autor:
Reihaneh Shafieian, Maryam Moghaddam Matin, Amin Rahpeyma, Alireza Fazel, Hamideh Salari Sedigh, Ariane Sadr-Nabavi, Halimeh Hassanzadeh, Alireza Ebrahimzadeh-Bideskan
Publikováno v:
Iranian Journal of Basic Medical Sciences, Vol 20, Iss 10, Pp 1131-1140 (2017)
Objective(s): Autologous bone transplantation known as the “gold standard” to reconstruction of osseous defects has known disadvantages. This study was designed to explore the effects of hydroxy-apatite/tricalcium-phosphate (HA/TCP) and platelet-
Externí odkaz:
https://doaj.org/article/587056eee51c41168f1db125bca849c6
Publikováno v:
Caspian Journal of Neurological Sciences, Vol 2, Iss 6, Pp 39-41 (2016)
Hereditary spastic paraplegias are highly heterogeneous neurodegenerative disorders with some special mutations. We report on a patient with pescavus, distal a myotrophy, hyper extended fingers, and pectus excavatum. Neurological examination showed t
Externí odkaz:
https://doaj.org/article/4e59d8105087480a8bfbd7db91e12b74
Autor:
Saeid Kargozar, Raheleh Baradaran, Javad Hami, Hossein Haghir, Hoda Khoshdel-Sarkarizi, Ariane Sadr-Nabavi, Abbas Mohammadipour, Mostafa Peyvandi Karizbodagh, Hamed Kheradmand
Publikováno v:
International Journal of Developmental Neuroscience. 80:303-318
The purpose of this study was to describe the distinct regional distribution patterns of expression of the α7 and α4 subunits of nicotinic acetylcholine receptors (nAChRs) and their left-right lateralisation in the rat hippocampus during the first
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fac3c16fa31e405a20913b8ebf0f689
https://doi.org/10.1002/jdn.10026
https://doi.org/10.1002/jdn.10026
Autor:
Mohammad Pourafshar, Ariane Sadr-Nabavi, Somayyeh Hashemian, Narjes Forouzanfar, Samaneh Vojdani, Mohammadreza Mirinezhad, Mohammad Ehsan Jaripour, Reza Jafarzadeh-Esfehani, Selma Zargari
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 33:355-359
Background Phenylketonuria (PKU) is a common metabolic disorder with great burden if left untreated or undiagnosed. Genetic variations in the phenylalanine hydroxylase (PAH) gene may be widely varied across different regions of a country. By knowing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1daf9beacba5e7d0ba3895c7457390a
https://doi.org/10.1515/jpem-2019-0351
https://doi.org/10.1515/jpem-2019-0351
Autor:
Barbara Garavaglia, Sadeq Vallian, Luigi M. Romito, Giulia Straccia, Marianna Capecci, Federica Invernizzi, Elisa Andrenelli, Arezu Kazemi, Sylvia Boesch, Robert Kopajtich, Nahid Olfati, Mohammad Shariati, Ali Shoeibi, Ariane Sadr-Nabavi, Holger Prokisch, Juliane Winkelmann, Michael Zech
Publikováno v:
Parkinsonismrelated disorders. 97
The genetic basis of autosomal-recessive dystonia remains poorly understood. Our objective was to report identification of additional individuals with variants in AOPEP, a recently described gene for recessively inherited dystonic disorders (OMIM:619
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2df9d65b39e151eb52b7854840154543
https://pubmed.ncbi.nlm.nih.gov/35306330
https://pubmed.ncbi.nlm.nih.gov/35306330