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Reza Boostani

Showing results (101-110 of 119) with videos related to

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Molecular Genetics & Genomic Medicine|September 16, 2020
Novel mutation identification and copy number variant detection via exome sequencing in congenital muscular dystrophyEdmund S Cauley, Alan Pittman, Swati Mummidivarpu, et al.
Iranian Journal of Public Health|June 24, 2024
Expanding the Clinical Phenotype of PLECTIN-Related PlectinopathiesParia Najarzadeh Torbati, Mohammad Doosti, Payam Sarraf, et al.
Neuromuscular Disorders : NMD|June 12, 2020
Hereditary polyneuropathy with optic atrophy due to PDXK variant leading to impaired Vitamin B6 metabolismNatalie Keller, Natalia Mendoza-Ferreira, Reza Maroofian, et al.
Acta Neurologica Belgica|July 4, 2024
Atypical presentations in an RTD patient and report of novel SLC52A3 and SLC52A2 mutationsDonya Sabeghi, Kolsoum InanlooRahatloo, Hanieh S Mirzadeh, et al.
Current Journal of Neurology|May 18, 2026
Translation and psychometric validation of the Persian version of amyotrophic lateral sclerosis cognitive behavioral screen (ALS-CBS) and revised amyotrophic lateral sclerosis functional rating scale (ALSFRS-R)Elnaz Naserzadeh, Nahid Olfati, Saeed Akhlaghi, et al.
Infection, Genetics and Evolution : Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases|May 19, 2019
Complete sequence of human T cell leukemia virus type 1 in ATLL patients from Northeast Iran, Mashhad revealed a prematurely terminated protease and an elongated pX open reading frame IIIAli Mirhosseini, Mehran Mohareri, Rohollah Arab, et al.
Frontiers in Neurology|October 8, 2021
Recommendations for Infantile-Onset and Late-Onset Pompe Disease: An Iranian ConsensusFarzad Fatehi, Mahmoud Reza Ashrafi, Marzieh Babaee, et al.
Human Mutation|February 18, 2021
Genomic variants causing mitochondrial dysfunction are common in hereditary lower motor neuron diseaseNatalie Keller, Cem Paketci, Janine Altmueller, et al.
Basic and Clinical Neuroscience|October 23, 2014
Operationalizing Cognitive Science and Technologies' Research and Development; the "Brain and Cognition Study Group (BCSG)" Initiative from Shiraz, IranNahid Ashjazadeh, Reza Boostani, Hamed Ekhtiari, et al.
Neurobiology of Aging|November 15, 2020
BVVL/ FL: features caused by SLC52A3 mutations; WDFY4 and TNFSF13B may be novel causative genesMarzieh Khani, Hosein Shamshiri, Hanieh Taheri, et al.
Pageof 12

Showing results (101-110 of 119) with videos related to

Sort By:
Pageof 12
Molecular Genetics & Genomic Medicine|September 16, 2020
Novel mutation identification and copy number variant detection via exome sequencing in congenital muscular dystrophyEdmund S Cauley, Alan Pittman, Swati Mummidivarpu, et al.
Iranian Journal of Public Health|June 24, 2024
Expanding the Clinical Phenotype of PLECTIN-Related PlectinopathiesParia Najarzadeh Torbati, Mohammad Doosti, Payam Sarraf, et al.
Neuromuscular Disorders : NMD|June 12, 2020
Hereditary polyneuropathy with optic atrophy due to PDXK variant leading to impaired Vitamin B6 metabolismNatalie Keller, Natalia Mendoza-Ferreira, Reza Maroofian, et al.
Acta Neurologica Belgica|July 4, 2024
Atypical presentations in an RTD patient and report of novel SLC52A3 and SLC52A2 mutationsDonya Sabeghi, Kolsoum InanlooRahatloo, Hanieh S Mirzadeh, et al.
Current Journal of Neurology|May 18, 2026
Translation and psychometric validation of the Persian version of amyotrophic lateral sclerosis cognitive behavioral screen (ALS-CBS) and revised amyotrophic lateral sclerosis functional rating scale (ALSFRS-R)Elnaz Naserzadeh, Nahid Olfati, Saeed Akhlaghi, et al.
Infection, Genetics and Evolution : Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases|May 19, 2019
Complete sequence of human T cell leukemia virus type 1 in ATLL patients from Northeast Iran, Mashhad revealed a prematurely terminated protease and an elongated pX open reading frame IIIAli Mirhosseini, Mehran Mohareri, Rohollah Arab, et al.
Frontiers in Neurology|October 8, 2021
Recommendations for Infantile-Onset and Late-Onset Pompe Disease: An Iranian ConsensusFarzad Fatehi, Mahmoud Reza Ashrafi, Marzieh Babaee, et al.
Human Mutation|February 18, 2021
Genomic variants causing mitochondrial dysfunction are common in hereditary lower motor neuron diseaseNatalie Keller, Cem Paketci, Janine Altmueller, et al.
Basic and Clinical Neuroscience|October 23, 2014
Operationalizing Cognitive Science and Technologies' Research and Development; the "Brain and Cognition Study Group (BCSG)" Initiative from Shiraz, IranNahid Ashjazadeh, Reza Boostani, Hamed Ekhtiari, et al.
Neurobiology of Aging|November 15, 2020
BVVL/ FL: features caused by SLC52A3 mutations; WDFY4 and TNFSF13B may be novel causative genesMarzieh Khani, Hosein Shamshiri, Hanieh Taheri, et al.
Pageof 12