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Massoud Houshmand

Showing results (91-100 of 161) with videos related to

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Archives of Medical Research|August 5, 2010
Two novel mutations in SCN1A gene in Iranian patients with epilepsyAhmad Ebrahimi, Massoud Houshmand, Seyed Hassan Tonekaboni, et al.
Archives of Medical Science : AMS|February 1, 2012
BAX pro-apoptotic gene alterations in repeated pregnancy lossSeyed Mohammad Seyedhassani, Massoud Houshmand, Seyed Mehdi Kalantar, et al.
European Journal of Clinical Investigation|March 30, 2011
8q24.3 and 11q25 chromosomal loci association with low HDL-C in metabolic syndromeMaryam Sadat Daneshpour, Ahmed Rebai, Massoud Houshmand, et al.
Journal of Child Neurology|February 25, 2014
Detection of intragenic SMN1 mutations in spinal muscular atrophy patients with a single copy of SMN1Hamid Ganji, Nayereh Nouri, Mansoor Salehi, et al.
Dementia and Geriatric Cognitive Disorders|August 21, 2014
Early-onset Alzheimer's disease in two Iranian families: a genetic studyMaryam Noroozian, Parisa Azadfar, Leila Akbari, et al.
Iranian Journal of Child Neurology|February 9, 2021
Novel Homozygous Pathogenic Mutations of LAMA 2 Gene in Patients with Congen ital Muscular DystrophyNegar Khodaenia, Zahra Farjami, Amir Hosein Ashnaei, et al.
Clinical Interventions in Aging|April 21, 2017
Association of genetic variations in the mitochondrial DNA control region with presbycusisMasoumeh Falah, Mohammad Farhadi, Seyed Kamran Kamrava, et al.
Iranian Journal of Child Neurology|November 16, 2020
A case report of congenital myasthenic syndrome caused by a mutation in theCHRNE genein the Iranian populationZahra Farjami, Negar Khodaenia, Neshat Ebrahimi, et al.
Molecular Biology Reports|July 1, 2014
A newly identified c.1824_1828dupATACG mutation in exon 13 of the GAA gene in infantile-onset glycogen storage disease type II (Pompe disease)Omid Aryani, Masoumeh Dehghan Manshadi, Mahdi Tondar, et al.
Urologia|May 19, 2021
CAG repeats and one polymorphism in androgen receptor gene are associated with renal calcium stone diseaseAbbas Basiri, Mohammad Naji, Massoud Houshmand, et al.
Pageof 17

Showing results (91-100 of 161) with videos related to

Sort By:
Pageof 17
Archives of Medical Research|August 5, 2010
Two novel mutations in SCN1A gene in Iranian patients with epilepsyAhmad Ebrahimi, Massoud Houshmand, Seyed Hassan Tonekaboni, et al.
Archives of Medical Science : AMS|February 1, 2012
BAX pro-apoptotic gene alterations in repeated pregnancy lossSeyed Mohammad Seyedhassani, Massoud Houshmand, Seyed Mehdi Kalantar, et al.
European Journal of Clinical Investigation|March 30, 2011
8q24.3 and 11q25 chromosomal loci association with low HDL-C in metabolic syndromeMaryam Sadat Daneshpour, Ahmed Rebai, Massoud Houshmand, et al.
Journal of Child Neurology|February 25, 2014
Detection of intragenic SMN1 mutations in spinal muscular atrophy patients with a single copy of SMN1Hamid Ganji, Nayereh Nouri, Mansoor Salehi, et al.
Dementia and Geriatric Cognitive Disorders|August 21, 2014
Early-onset Alzheimer's disease in two Iranian families: a genetic studyMaryam Noroozian, Parisa Azadfar, Leila Akbari, et al.
Iranian Journal of Child Neurology|February 9, 2021
Novel Homozygous Pathogenic Mutations of LAMA 2 Gene in Patients with Congen ital Muscular DystrophyNegar Khodaenia, Zahra Farjami, Amir Hosein Ashnaei, et al.
Clinical Interventions in Aging|April 21, 2017
Association of genetic variations in the mitochondrial DNA control region with presbycusisMasoumeh Falah, Mohammad Farhadi, Seyed Kamran Kamrava, et al.
Iranian Journal of Child Neurology|November 16, 2020
A case report of congenital myasthenic syndrome caused by a mutation in theCHRNE genein the Iranian populationZahra Farjami, Negar Khodaenia, Neshat Ebrahimi, et al.
Molecular Biology Reports|July 1, 2014
A newly identified c.1824_1828dupATACG mutation in exon 13 of the GAA gene in infantile-onset glycogen storage disease type II (Pompe disease)Omid Aryani, Masoumeh Dehghan Manshadi, Mahdi Tondar, et al.
Urologia|May 19, 2021
CAG repeats and one polymorphism in androgen receptor gene are associated with renal calcium stone diseaseAbbas Basiri, Mohammad Naji, Massoud Houshmand, et al.
Pageof 17