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Mohammad Reza Alaei

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Iranian Journal of Child Neurology|February 7, 2015
Validation of Urinary Glycosaminoglycans in Iranian patients with Mucopolysaccharidase type I: The effect of urine sedimentation characteristicsMohammad Abdi, Mohammad Said Hakhamaneshi, Mohammad Reza Alaei, et al.
Iranian Journal of Child Neurology|February 28, 2022
Next-generation sequencing identified novel truncating mutations in BBS9 causing Bardet Biedl syndrome in two Iranian consanguineous familiesSusan Akbaroghli, Daniz Kooshavar, Zahra Golchehre, et al.
International Journal of Molecular and Cellular Medicine|November 9, 2023
Mutational Analysis and Genotype Investigation of Less Known Gaucher Mutations through Haplotype Analysis in Iranian Gaucher PatientsNegar Sardarpour, Hamideh Bagherian, Fatemeh Zafarghandi Motlagh, et al.
Mutation Research|February 23, 2016
Identification of six novel mutations in Iranian patients with maple syrup urine disease and their in silico analysisMaryam Abiri, Razieh Karamzadeh, Morteza Karimipoor, et al.
JIMD Reports|May 27, 2015
Molecular Characterization of QDPR Gene in Iranian Families with BH4 Deficiency: Reporting Novel and Recurrent MutationsHannaneh Foroozani, Maryam Abiri, Shadab Salehpour, et al.
Metabolic Brain Disease|August 11, 2016
In silico analysis of novel mutations in maple syrup urine disease patients from IranMaryam Abiri, Razieh Karamzadeh, Marziyeh Mojbafan, et al.
Immunological Investigations|January 12, 2021
The Prevalence of Selective and Partial Immunoglobulin A Deficiency in Patients with Autoimmune PolyendocrinopathyMahnaz Jamee, Mohammad Reza Alaei, Mehrnaz Mesdaghi, et al.
Endocrine, Metabolic & Immune Disorders Drug Targets|September 13, 2023
Immunological Evaluation of Pediatric Patients with PolyautoimmunityFatemeh Sadat Mahdavi, Marzieh Tavakol, Fatemeh Aghamahdi, et al.
Indian Pediatrics|January 6, 2023
Inborn Errors of Metabolism Associated With Autism Among Children: A Multicenter Study from IranHossein Moravej, Soroor Inaloo, Saman Nahid, et al.
Journal of Inherited Metabolic Disease|August 31, 2018
Molecular genetics of a cohort of 635 cases of phenylketonuria in a consanguineous populationTina Shirzadeh, Amir Hossein Saeidian, Hamideh Bagherian, et al.
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Showing results (21-30 of 30) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
Iranian Journal of Child Neurology|February 7, 2015
Validation of Urinary Glycosaminoglycans in Iranian patients with Mucopolysaccharidase type I: The effect of urine sedimentation characteristicsMohammad Abdi, Mohammad Said Hakhamaneshi, Mohammad Reza Alaei, et al.
Iranian Journal of Child Neurology|February 28, 2022
Next-generation sequencing identified novel truncating mutations in BBS9 causing Bardet Biedl syndrome in two Iranian consanguineous familiesSusan Akbaroghli, Daniz Kooshavar, Zahra Golchehre, et al.
International Journal of Molecular and Cellular Medicine|November 9, 2023
Mutational Analysis and Genotype Investigation of Less Known Gaucher Mutations through Haplotype Analysis in Iranian Gaucher PatientsNegar Sardarpour, Hamideh Bagherian, Fatemeh Zafarghandi Motlagh, et al.
Mutation Research|February 23, 2016
Identification of six novel mutations in Iranian patients with maple syrup urine disease and their in silico analysisMaryam Abiri, Razieh Karamzadeh, Morteza Karimipoor, et al.
JIMD Reports|May 27, 2015
Molecular Characterization of QDPR Gene in Iranian Families with BH4 Deficiency: Reporting Novel and Recurrent MutationsHannaneh Foroozani, Maryam Abiri, Shadab Salehpour, et al.
Metabolic Brain Disease|August 11, 2016
In silico analysis of novel mutations in maple syrup urine disease patients from IranMaryam Abiri, Razieh Karamzadeh, Marziyeh Mojbafan, et al.
Immunological Investigations|January 12, 2021
The Prevalence of Selective and Partial Immunoglobulin A Deficiency in Patients with Autoimmune PolyendocrinopathyMahnaz Jamee, Mohammad Reza Alaei, Mehrnaz Mesdaghi, et al.
Endocrine, Metabolic & Immune Disorders Drug Targets|September 13, 2023
Immunological Evaluation of Pediatric Patients with PolyautoimmunityFatemeh Sadat Mahdavi, Marzieh Tavakol, Fatemeh Aghamahdi, et al.
Indian Pediatrics|January 6, 2023
Inborn Errors of Metabolism Associated With Autism Among Children: A Multicenter Study from IranHossein Moravej, Soroor Inaloo, Saman Nahid, et al.
Journal of Inherited Metabolic Disease|August 31, 2018
Molecular genetics of a cohort of 635 cases of phenylketonuria in a consanguineous populationTina Shirzadeh, Amir Hossein Saeidian, Hamideh Bagherian, et al.
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