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Biological Trace Element Research
|
April 13, 2019
Oxidative Stress Parameters, Trace Elements, and Lipid Profile in Iranian Patients with Gaucher Disease
Hadi Mozafari, Shohreh Khatami, Amir Kiani, et al.
Iranian Journal of Child Neurology
|
July 20, 2021
Clinical and Paraclinical Characteristics of Non-Classic Phenylketonuria
Marjan Shakiba, Hedyeh Saneifard, Mohammad Reza Alaei, et al.
Molecular Genetics and Metabolism Reports
|
July 15, 2024
Expanded inherited metabolic diseases screening by tandem mass spectrophotometry: The first report from Iran
Marjan Shakiba, Mehrdad Yasaei, Hedyeh Saneifard, et al.
Iranian Biomedical Journal
|
December 21, 2025
Novel FKBP10 Mutation in Iranian Patients with Osteogenesis Imperfecta: Insights from Whole-Exome Sequencing to Molecular Dynamics
Moslem Hoseinbeyki, Shirin Moradifard, Fatemeh Mirkhani, et al.
Iranian Biomedical Journal
|
December 30, 2023
Identification of Novel Mutations in the MMAA and MUT Genes among Methylmalonic Aciduria Families
Mahboobeh Jafari, Fatemeh Karami, Aria Setoodeh, et al.
Trials
|
December 28, 2021
Study protocol of a randomized controlled clinical trial investigating the effects of omega-3 supplementation on endothelial function, vascular structure, and metabolic parameters in adolescents with type 1 diabetes
Masoud Khorshidi, Aliakbar Sayyari, Beheshteh Olang, et al.
Iranian Journal of Child Neurology
|
July 20, 2021
Analysis of glucocerebrosidase (GBA) gene mutations in Iranian patients with Gaucher disease
Hadi Mozafari, Mohammad Tghikhani, Zohreh Rahimi, et al.
Iranian Journal of Medical Sciences
|
November 2, 2012
ELISA Cut-off Point for the Diagnosis of Human Brucellosis; a Comparison with Serum Agglutination Test
Anahita Sanaei Dashti, Abdollah Karimi, Vadood Javad, et al.
Molecular Biology Reports
|
December 11, 2025
Genetic variability in maple syrup urine disease: novel mutations and their pathogenicity in the Iranian population
Mansooreh Jafari, Fatemeh Karami, Iman Salahshourifar, et al.
Indian Journal of Clinical Biochemistry : IJCB
|
June 20, 2015
Determination of Biological Variance and Validation of a Fluorometric Assay for Measurement of α-l-Iduronidase Activity in Dried Blood Spots Samples: The First Experience in Iran
Mohammad Abdi, Mohammad Said Hakhamaneshi, Mohammad Reza Alaei, et al.
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Search research articles
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Showing results (11-20 of 30) with videos related to
Sort By:
Page
of 3
Biological Trace Element Research
|
April 13, 2019
Oxidative Stress Parameters, Trace Elements, and Lipid Profile in Iranian Patients with Gaucher Disease
Hadi Mozafari, Shohreh Khatami, Amir Kiani, et al.
Iranian Journal of Child Neurology
|
July 20, 2021
Clinical and Paraclinical Characteristics of Non-Classic Phenylketonuria
Marjan Shakiba, Hedyeh Saneifard, Mohammad Reza Alaei, et al.
Molecular Genetics and Metabolism Reports
|
July 15, 2024
Expanded inherited metabolic diseases screening by tandem mass spectrophotometry: The first report from Iran
Marjan Shakiba, Mehrdad Yasaei, Hedyeh Saneifard, et al.
Iranian Biomedical Journal
|
December 21, 2025
Novel FKBP10 Mutation in Iranian Patients with Osteogenesis Imperfecta: Insights from Whole-Exome Sequencing to Molecular Dynamics
Moslem Hoseinbeyki, Shirin Moradifard, Fatemeh Mirkhani, et al.
Iranian Biomedical Journal
|
December 30, 2023
Identification of Novel Mutations in the MMAA and MUT Genes among Methylmalonic Aciduria Families
Mahboobeh Jafari, Fatemeh Karami, Aria Setoodeh, et al.
Trials
|
December 28, 2021
Study protocol of a randomized controlled clinical trial investigating the effects of omega-3 supplementation on endothelial function, vascular structure, and metabolic parameters in adolescents with type 1 diabetes
Masoud Khorshidi, Aliakbar Sayyari, Beheshteh Olang, et al.
Iranian Journal of Child Neurology
|
July 20, 2021
Analysis of glucocerebrosidase (GBA) gene mutations in Iranian patients with Gaucher disease
Hadi Mozafari, Mohammad Tghikhani, Zohreh Rahimi, et al.
Iranian Journal of Medical Sciences
|
November 2, 2012
ELISA Cut-off Point for the Diagnosis of Human Brucellosis; a Comparison with Serum Agglutination Test
Anahita Sanaei Dashti, Abdollah Karimi, Vadood Javad, et al.
Molecular Biology Reports
|
December 11, 2025
Genetic variability in maple syrup urine disease: novel mutations and their pathogenicity in the Iranian population
Mansooreh Jafari, Fatemeh Karami, Iman Salahshourifar, et al.
Indian Journal of Clinical Biochemistry : IJCB
|
June 20, 2015
Determination of Biological Variance and Validation of a Fluorometric Assay for Measurement of α-l-Iduronidase Activity in Dried Blood Spots Samples: The First Experience in Iran
Mohammad Abdi, Mohammad Said Hakhamaneshi, Mohammad Reza Alaei, et al.
Page
of 3