Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Mohammad Vafaee Shahi"'
Autor:
Mohammad Vafaee Shahi, Sedigheh Yousefzadegan, Ramin Zare Mahmoudabadi, Fatemeh Ahmadi, Aina Riahi
Publikováno v:
Türk Nöroloji Dergisi, Vol 27, Iss s1, Pp 46-48 (2021)
Brain ischemic stroke in children, especially in infancy, is a rare condition. Stroke presents a variety of symptoms and usually is an underestimated diagnosis in infants. The current coronavirus disease-2019 (COVID-19) pandemic involves different or
Externí odkaz:
https://doaj.org/article/0d96d4f00c9c45df9bdafde6563c376c
Publikováno v:
Clinical Case Reports, Vol 12, Iss 8, Pp n/a-n/a (2024)
Key Clinical Message Necrotizing pneumonia (NP) is the destruction of the interstitial part of the lung due to severe infection. One cause of this rare and fatal condition in pediatrics is Acinetobacter. Severe infections, especially pneumonia, can p
Externí odkaz:
https://doaj.org/article/425ff86176494a5f82eef3a347635632
Autor:
Ahmad Daneshi, Masoud Garshasbi, Mohammad Farhadi, Khalil Ghasemi Falavarjani, Mohammad Vafaee-Shahi, Navid Almadani, MohammadSina Zabihi, Mohammad Amin Ghalavand, Masoumeh Falah
Publikováno v:
BMC Medical Genomics, Vol 16, Iss 1, Pp 1-22 (2023)
Abstract Background Mutations in ABHD12 (OMIM: 613,599) are associated with polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract (PHARC) syndrome (OMIM: 612674), which is a rare autosomal recessive neurodegenerative disease. PHARC
Externí odkaz:
https://doaj.org/article/3d3039bb6e094fa08737ec43ea18b442
Autor:
Haide Golsorkhi, Mostafa Qorbani, Mohammad Kamalinejad, Saeideh Sabbaghzadegan, Mohsen Bahrami, Mohammad Vafaee-Shahi, Hadi Montazerlotfelahi, Elham Abniki, Majid Dadmehr
Publikováno v:
Trials, Vol 23, Iss 1, Pp 1-7 (2022)
Abstract Background Attention-deficit/hyperactivity disorder (ADHD) is the most common behavioral disorder in childhood and adolescence. A number of these patients do not respond to the current pharmacological treatments and there may also be drug si
Externí odkaz:
https://doaj.org/article/520cf40dd0ca4b4393153d0ffa037ca4
Autor:
Mohammad Vafaee‐Shahi, Saeide Ghasemi, Mehran Beiraghi Toosi, Mahmoud Reza Ashrafi, Reza Shervin Badv, Ali Reza Tavasoli, Leila Tahernia
Publikováno v:
Clinical Case Reports, Vol 9, Iss 9, Pp n/a-n/a (2021)
Abstract We report a patient with complex clinical presentation including multiple neurological symptoms and eye involvement. Upon genetic investigation, the patient was found to carry a novel homozygous mutation in the NDUFS4 gene, thus adding to th
Externí odkaz:
https://doaj.org/article/58d33fd325714bb888c58f92bad9772c
Autor:
Vahid Mansouri, Morteza Heidari, Maryam Bemanalizadeh, Reza Azizimalamiri, Shahriar Nafissi, Masood Ghahvechi Akbari, Mohammad Barzegar, Ali Reza Moayedi, Reza Shervin Badv, Mahmood Mohamadi, Ali Reza Tavasoli, Susan Amirsalari, Ali Khajeh, Soroor Inaloo, Farzad Fatehi, Sareh Hosseinpour, Meisam Babaei, Seyed Ahmad Hosseini, Seyyed Mohammad Mahdi Hosseiny, Afshin Fayyazi, Firoozeh Hosseini, Mehran Beiraghi Toosi, Nahid Khosroshahi, Homa Ghabeli, Habibeh Nejad Biglari, Simin Khayatzadeh Kakhki, Seyed Hossein Mirlohi, Elham Bidabadi, Bahram Mohammadi, Abdolmajid Omrani, Mostafa Sedighi, Mohammad Vafaee-Shahi, Maryam Rasulinezhad, Seyyed Mohamad Hoseini, Mojtaba Movahedinia, Zahra Rezaei, Parviz Karimi, Hossein Farshadmoghadam, Saeed Anvari, Omid Yaghini, Jafar Nasiri, Gholamreza Zamani, Mahmoud Reza Ashrafi
Publikováno v:
Journal of Neuromuscular Diseases. 10:211-225
Background: Insufficient amounts of survival motor neuron protein is leading to one of the most disabling neuromuscular diseases, spinal muscular atrophy (SMA). Before the current study, the detailed characteristics of Iranian patients with SMA had n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1050f12b1ad45d5c6285a65d7c6b2244
https://doi.org/10.3233/jnd-221614
https://doi.org/10.3233/jnd-221614
Autor:
Mohammad Hassan Bemanian, Saba Arshi, Mohammad Nabavi, Mohammad Vafaee-Shahi, Morteza Fallahpour, Sima Shokri, Afshin Rezaeifar, Hossein Shahzadi, Fatemeh Atashrazm
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 20, Iss 2 (2021)
Immunodeficiency, centromeric instability, and facial anomalies (ICF) syndrome is a rare primary immunodeficiency disorder characterized by recurrent infections and low immunoglobulin levels due to variable combined immunodeficiency, and centromeric
Externí odkaz:
https://doaj.org/article/e9f9c4e763e64b26b2ea20b0d1a7380f
Publikováno v:
Contemporary Clinical Neuroscience ISBN: 9783031231032
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b629b2de80dc112537862ca81a863eb
https://doi.org/10.1007/978-3-031-23104-9_22
https://doi.org/10.1007/978-3-031-23104-9_22
Publikováno v:
The Open Neurology Journal. 15:59-64
Background: Sodium valproate is an antiepileptic drug primarily used to treat status epilepticus [SE]; however, its effect on cardiac function is unclear. This study aimed to examine the effect of 6 months of sodium valproate treatment on the cardiac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f9835511cad24749b523a575099f47d
https://doi.org/10.2174/1874205x02115010059
https://doi.org/10.2174/1874205x02115010059
Autor:
Mohammad Vafaee-Shahi, Samileh Noorbakhsh, Elham Shirazi, Mehrnoosh Purfallah, Saeideh Ghasemi, Aina Riahi
Publikováno v:
The Open Public Health Journal. 15
Background: Attention deficit hyperactivity disorder (ADHD) is a common behavioral problem in children. Identifying the associated risk factors of ADHD is very important for the prognosis and early diagnosis of the disease. Here, we evaluated the ass
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f20ec654b2cffc17b133c3bb8130a28c
https://doi.org/10.2174/18749445-v15-e221219-2022-64
https://doi.org/10.2174/18749445-v15-e221219-2022-64