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Ali Nikkhah

Showing results (31-40 of 40) with videos related to

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Cancer Cell International|August 24, 2021
The impact of LncRNA dysregulation on clinicopathology and survival of pancreatic cancer: a systematic review and meta-analysis (PRISMA compliant)Elahe Seyed Hosseini, Ali Nikkhah, Amir Sotudeh, et al.
Iranian Journal of Child Neurology|February 1, 2023
Clinical and MRI characteristics of multiple sclerosis in Iranian Children and AdolescentsMohammad Mahdi Nasehi, Ali Nikkhah, Sasan Saket, et al.
Journal of Molecular Neuroscience : MN|March 14, 2026
TASP1-Related Suleiman-El-Hattab Syndrome: The First Genetically Confirmed Case in Iran Accompanied by a Comprehensive Literature ReviewNarges Mashayekhi, Alireza Zangooie, Reza Asgari, et al.
Movement Disorders Clinical Practice|May 19, 2023
Familial Hypermanganesemia in IranSeyedeh Narges Tabatabaee, Sajjad Effat Nejad, Ali Nikkhah, et al.
Clinical Case Reports|December 10, 2025
A Novel Mutation of CADHERIN (<i>CDH15</i>) in an Iranian Boy With Borderline Intelligence Without Dysmorphism-A Case ReportMahmoud Reza Ashrafi, Ali Nikkhah, Morteza Heidari, et al.
Iranian Journal of Child Neurology|August 28, 2023
Neurological Involvements in COVID-19: A hospital-based studyHadi Montazerlotfelahi, Mahsa Norouzi, Forough Askarimoghaddam, et al.
Stem Cell Research & Therapy|February 22, 2026
Safety and feasibility of intravenous fresh adipose-derived mesenchymal stem cells in secondary progressive multiple sclerosis: phase I/IIa clinical resultsFahimeh Lavi Arab, Forouzan Yousefi, Hojjat Naderi-Meshkin, et al.
Human Genomics|April 3, 2024
The genetic basis of early-onset hereditary ataxia in Iran: results of a national registry of a heterogeneous populationNejat Mahdieh, Morteza Heidari, Zahra Rezaei, et al.
Neurogenetics|September 5, 2023
Correction to: High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy RegistryMahmoudreza Ashrafi, Reyhaneh Kameli, Sareh Hosseinpour, et al.
Neurogenetics|August 19, 2023
High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy RegistryMahmoudreza Ashrafi, Reyhaneh Kameli, Sareh Hosseinpour, et al.
Pageof 4

Showing results (31-40 of 40) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 40 results.
Cancer Cell International|August 24, 2021
The impact of LncRNA dysregulation on clinicopathology and survival of pancreatic cancer: a systematic review and meta-analysis (PRISMA compliant)Elahe Seyed Hosseini, Ali Nikkhah, Amir Sotudeh, et al.
Iranian Journal of Child Neurology|February 1, 2023
Clinical and MRI characteristics of multiple sclerosis in Iranian Children and AdolescentsMohammad Mahdi Nasehi, Ali Nikkhah, Sasan Saket, et al.
Journal of Molecular Neuroscience : MN|March 14, 2026
TASP1-Related Suleiman-El-Hattab Syndrome: The First Genetically Confirmed Case in Iran Accompanied by a Comprehensive Literature ReviewNarges Mashayekhi, Alireza Zangooie, Reza Asgari, et al.
Movement Disorders Clinical Practice|May 19, 2023
Familial Hypermanganesemia in IranSeyedeh Narges Tabatabaee, Sajjad Effat Nejad, Ali Nikkhah, et al.
Clinical Case Reports|December 10, 2025
A Novel Mutation of CADHERIN (<i>CDH15</i>) in an Iranian Boy With Borderline Intelligence Without Dysmorphism-A Case ReportMahmoud Reza Ashrafi, Ali Nikkhah, Morteza Heidari, et al.
Iranian Journal of Child Neurology|August 28, 2023
Neurological Involvements in COVID-19: A hospital-based studyHadi Montazerlotfelahi, Mahsa Norouzi, Forough Askarimoghaddam, et al.
Stem Cell Research & Therapy|February 22, 2026
Safety and feasibility of intravenous fresh adipose-derived mesenchymal stem cells in secondary progressive multiple sclerosis: phase I/IIa clinical resultsFahimeh Lavi Arab, Forouzan Yousefi, Hojjat Naderi-Meshkin, et al.
Human Genomics|April 3, 2024
The genetic basis of early-onset hereditary ataxia in Iran: results of a national registry of a heterogeneous populationNejat Mahdieh, Morteza Heidari, Zahra Rezaei, et al.
Neurogenetics|September 5, 2023
Correction to: High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy RegistryMahmoudreza Ashrafi, Reyhaneh Kameli, Sareh Hosseinpour, et al.
Neurogenetics|August 19, 2023
High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy RegistryMahmoudreza Ashrafi, Reyhaneh Kameli, Sareh Hosseinpour, et al.
Pageof 4