檢索結果 - Mohammad Rohani
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A novel homozygous variation in the PANK2 gene in two Persian siblings with atypical pantothenate kinase associated neurodegeneration 由 Amir Hasan Habibi, Saeed Razmeh, Omid Aryani, Mohammad Rohani, Laleh Taghavian, Elham Alizadeh, Karim Moradian Kokhedan, Maryam Zaribafian
發表在 Neurology International (2019-03-01)獲取全文
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Exploring functional neurological disorder: Cultural influences and risk factors in Iranian society – A cross-sectional study 由 Tina Moghadam Fard, Abdol-Hossein Vahabie, MohammadAli Shokri, Mohammad Rohani, Maziar Emamikhah, Soode Tajik Esmaeeli, Seyed Amir Hassan Habibi, Fatemeh Sadat Mirfazeli
發表在 Brain Disorders (2025-09-01)獲取全文
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Evaluation of the effect of Modafinil in the improvement of the level of consciousness in patients with COVID‐19 encephalopathy: A randomized controlled trial 由 Fatemeh Talebi Kiasari, Mobin Naghshbandi, Maziar Emamikhah, Omid Moradi Moghaddam, Mohammad Niakan Lahiji, Mohammad Rohani, Narges Yazdi, Hamidreza Movahedi, Alireza Amanollahi, Pardis Irandoost, Roya Ghafoury
發表在 Neuropsychopharmacology Reports (2024-09-01)獲取全文
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Posterior reversible encephalopathy syndrome in SARS‐CoV‐2 infection: A case report and review of literature 由 Mahsa Ziaee, Maryam Saeedi, Mohammad Rohani, Masoud Mehrpour, Bahram Haghi Ashtiani, Babak Zamani, Fahimeh Haji Akhoundi, Misagh Salahi Khalaf, Seyyedmohammadsadeq Mirmoeeni, Amirhossein Azari Jafari, Zahra Shateri
發表在 Clinical Case Reports (2023-04-01)獲取全文
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Correction: Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients 由 Ali Zare Dehnavi, Maryam Bemanalizadeh, Seyyed Mohammad Kahani, Mahmoud Reza Ashrafi, Mohammad Rohani, Mehran Beiraghi Toosi, Morteza Heidari, Sareh Hosseinpour, Behnam Amini, Shaghayegh Zokaei, Zahra Rezaei, Hajar Aryan, Man Amanat, Hassan Vahidnezhad, Pouria Mohammadi, Masoud Garshasbi, Ali Reza Tavasoli
發表在 Orphanet Journal of Rare Diseases (2023-07-01)獲取全文
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Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients 由 Ali Zare Dehnavi, Maryam Bemanalizadeh, Seyyed Mohammad Kahani, Mahmoud Reza Ashrafi, Mohammad Rohani, Mehran Beiraghi Toosi, Morteza Heidari, Sareh Hosseinpour, Behnam Amini, Shaghayegh Zokaei, Zahra Rezaei, Hajar Aryan, Man Amanat, Hassan Vahidnezhad, Pouria Mohammadi, Masoud Garshasbi, Ali Reza Tavasoli
發表在 Orphanet Journal of Rare Diseases (2023-07-01)獲取全文
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The genetic basis of early-onset hereditary ataxia in Iran: results of a national registry of a heterogeneous population 由 Nejat Mahdieh, Morteza Heidari, Zahra Rezaei, Ali Reza Tavasoli, Sareh Hosseinpour, Maryam Rasulinejad, Ali Zare Dehnavi, Masoud Ghahvechi Akbari, Reza Shervin Badv, Elahe Vafaei, Ali Mohebbi, Pouria Mohammadi, Seyyed Mohammad Mahdi Hosseiny, Reza Azizimalamiri, Ali Nikkhah, Elham Pourbakhtyaran, Mohammad Rohani, Narges Khanbanha, Sedigheh Nikbakht, Mojtaba Movahedinia, Parviz Karimi, Homa Ghabeli, Seyed Ahmad Hosseini, Fatemeh Sadat Rashidi, Masoud Garshasbi, Morteza Rezvani Kashani, Noor M. Ghiasvand, Stephan Zuchner, Matthis Synofzik, Mahmoud Reza Ashrafi
發表在 Human Genomics (2024-04-01)獲取全文
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