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Shahriar Nafissi

Showing results (1-10 of 155) with videos related to

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Iranian Journal of Neurology|November 26, 2014
Comparison of electrophysiological findings in axonal and demyelinating Guillain-Barre syndromeSamira Yadegari, Shahriar Nafissi, Neda Kazemi
Neurosciences (Riyadh, Saudi Arabia)|July 10, 2012
Protracted disease course after deafness in a man with Brown-Vialetto-Van Laere syndromeSamira Yadegari, Keyvan Razmjoo, Shahriar Nafissi
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|May 3, 2014
Clinical and electrophysiological features of Guillain-Barré syndrome in IranSamira Yadegari, Neda Kazemi, Shahriar Nafissi
Case Reports in Rheumatology|January 30, 2024
A New Case of Granulomatosis with Polyangiitis Presented with Tolosa-Hunt Syndrome ManifestationsMaryam Mohebbi, Shahriar Nafissi, Majid Alikhani
Iranian Journal of Neurology|November 20, 2013
Electrophysiological evaluation in lumbosacral radiculopathyShahriar Nafissi, Shahram Niknam, Seyedeh Simindokht Hosseini
Neurosciences (Riyadh, Saudi Arabia)|April 3, 2012
Chronic inflammatory demyelinating polyneuropathy following malignant melanomaMohamad B Dbouk, Shahriar Nafissi, Askar Ghorbani
Journal of Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society|December 3, 2015
Blink Reflex May Help Discriminate Alzheimer Disease From Vascular DementiaFatemeh Mohammadian, Maryam Noroozian, Shahriar Nafissi, et al.
Neuromuscular Disorders : NMD|March 29, 2025
Identifying novel AGRN variants in congenital myasthenic syndrome: insights from three Iranian familiesHadi Gharebaghian, Aida Ghasemi, Omid Hesami, et al.
Iranian Journal of Neurology|November 20, 2013
Factors affecting bone mineral density in multiple sclerosis patientsAzin Ayatollahi, Mohammad Reza Mohajeri-Tehrani, Shahriar Nafissi
Iranian Journal of Neurology|December 2, 2015
Observation of c.260A > G mutation in superoxide dismutase 1 that causes p.Asn86Ser in Iranian amyotrophic lateral sclerosis patient and absence of genotype/phenotype correlationMarzieh Khani, Afagh Alavi, Shahriar Nafissi, et al.
Pageof 16

Showing results (1-10 of 155) with videos related to

Sort By:
Pageof 16
Iranian Journal of Neurology|November 26, 2014
Comparison of electrophysiological findings in axonal and demyelinating Guillain-Barre syndromeSamira Yadegari, Shahriar Nafissi, Neda Kazemi
Neurosciences (Riyadh, Saudi Arabia)|July 10, 2012
Protracted disease course after deafness in a man with Brown-Vialetto-Van Laere syndromeSamira Yadegari, Keyvan Razmjoo, Shahriar Nafissi
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|May 3, 2014
Clinical and electrophysiological features of Guillain-Barré syndrome in IranSamira Yadegari, Neda Kazemi, Shahriar Nafissi
Case Reports in Rheumatology|January 30, 2024
A New Case of Granulomatosis with Polyangiitis Presented with Tolosa-Hunt Syndrome ManifestationsMaryam Mohebbi, Shahriar Nafissi, Majid Alikhani
Iranian Journal of Neurology|November 20, 2013
Electrophysiological evaluation in lumbosacral radiculopathyShahriar Nafissi, Shahram Niknam, Seyedeh Simindokht Hosseini
Neurosciences (Riyadh, Saudi Arabia)|April 3, 2012
Chronic inflammatory demyelinating polyneuropathy following malignant melanomaMohamad B Dbouk, Shahriar Nafissi, Askar Ghorbani
Journal of Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society|December 3, 2015
Blink Reflex May Help Discriminate Alzheimer Disease From Vascular DementiaFatemeh Mohammadian, Maryam Noroozian, Shahriar Nafissi, et al.
Neuromuscular Disorders : NMD|March 29, 2025
Identifying novel AGRN variants in congenital myasthenic syndrome: insights from three Iranian familiesHadi Gharebaghian, Aida Ghasemi, Omid Hesami, et al.
Iranian Journal of Neurology|November 20, 2013
Factors affecting bone mineral density in multiple sclerosis patientsAzin Ayatollahi, Mohammad Reza Mohajeri-Tehrani, Shahriar Nafissi
Iranian Journal of Neurology|December 2, 2015
Observation of c.260A > G mutation in superoxide dismutase 1 that causes p.Asn86Ser in Iranian amyotrophic lateral sclerosis patient and absence of genotype/phenotype correlationMarzieh Khani, Afagh Alavi, Shahriar Nafissi, et al.
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