Publications by authors named "Majid Aminzadeh"

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Exome Sequencing Reveals Novel Variants in Genetic Skeletal Disorders: Insights From a Cohort in Southwest Iran.
Rezvan Zabihi, Mina Zamani, Niloofar Chamanrou, Jawaher Zeighami, Tahere Seifi, Majid Aminzadeh

Clin Genet· September 2025

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Safety and effectiveness of a biosimilar somatropin (Cinnatropin®) in children and adolescents receiving growth hormone therapy over 1 year: a registry-based phase IV study.
Ali Rabbani, Maryam Razzaghy-Azar, Zohreh Karamizadeh, Mahin Hashemipour, Rahim Vakili, Majid Aminzadeh

Eur J Pediatr· March 2025

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Identification of the mutations in BTD gene in Iranian patients with biotinidase deficiency and evaluating their genotype-phenotype correlations.
Fatemeh Azizinejad, Majid Aminzadeh, Maryam Tahmasebi-Birgani, Solmaz Heidari, Pegah Ghandil

Gene· January 2025

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Genetic features of patients with MPS type IIIB: Description of five pathogenic gene variations.
Mahzad Nasir Shalal, Majid Aminzadeh, Alihossein Saberi, Reza Azizi Malmiri, Reza Aminzadeh

Gene· June 2024

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Identification of new variants in patients with mucopolysaccharidosis in consanguineous Iranian families.
Rezvan Zabihi, Mina Zamani, Majid Aminzadeh, Niloofar Chamanrou, Fatemeh Zahra Kiani

Front Genet· February 2024

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Measurement of the Neutrophils Count and Oxidative Burst in Neutrophils of Patients with Sanjad Sakati Syndrome.
Farhad Abolnezhadian, Majid Aminzadeh, Sara Iranparast, Sajad Dehnavi, Fatemeh Dousti

Iran J Allergy Asthma Immunol· February 2024

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Inborn Errors of Metabolism Associated With Autism Among Children: A Multicenter Study from Iran.
Hossein Moravej, Soroor Inaloo, Saman Nahid, Shokrollah Mazloumi, Hamid Nemati, Majid Aminzadeh

Indian Pediatr· March 2023

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Molecular characterization of a large cohort of mucopolysaccharidosis patients: Iran Mucopolysaccharidosis RE-diagnosis study (IMPRESsion).
Saeed R Ghaffari, Maryam Rafati, Mahdi Shadnoush, Shokooh Pourbabaee, Mohammad Aghighi, Majid Aminzadeh

Hum Mutat· April 2022

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Association of vitamin D status with COVID-19 disease severity in pediatric patients: A retrospective observational study.
Solmaz Heidari, Shooka Mohammadi, Mohammadreza Fathi, Shayan Cigary, Mohsen Alisamir, Majid Aminzadeh

Health Sci Rep· April 2022

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Molecular diagnosis of maturity onset diabetes of the young in Iranian patients: improving management.
Fatemeh Davoudi, Majid Aminzadeh, Hajiye Bibi Shahbazian, Mahdi Bijanzadeh, Ata A Ghadiri

J Diabetes Metab Disord· December 2021

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Changes in body mass index after pediatric renal transplantation.
Seyed Seifollah Beladi Mousavi, Ehsan Valavi, Majid Aminzadeh, Heshmatollah Shahbazian, Hasan Otukesh

Saudi J Kidney Dis Transpl· April 2021

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Author's reply.
Ehsan Valavi, Majid Aminzadeh

Saudi J Kidney Dis Transpl· January 2021

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Clinical features and tubulin folding cofactor E gene analysis in Iranian patients with Sanjad-Sakati syndrome.
Majid Aminzadeh, Hamid Galehdari, Gholamreza Shariati, Nasrin Malekpour, Pegah Ghandil

J Pediatr (Rio J)· September 2020

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Effect of prednisolone on linear growth in children with nephrotic syndrome.
Ehsan Valavi, Majid Aminzadeh, Parisa Amouri, Afshin Rezazadeh, Maedeh Beladi-Mousavi

J Pediatr (Rio J)· September 2020

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The Effects of Synbiotic Supplementation on Glycemic Status, Lipid Profile, and Biomarkers of Oxidative Stress in Type 1 Diabetic Patients. A Placebo-Controlled, Double-Blind, Randomized Clinical Trial.
Ahmad Zare Javid, Majid Aminzadeh, Mohammad Hosein Haghighi-Zadeh, Mona Jamalvandi

Diabetes Metab Syndr Obes· March 2020

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Thyroid scintigraphy in three-year-old children with congenital hypothyroidism in correlation with neonatal TSH.
Majid Aminzadeh

Endokrynol Pol· July 2019

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Identification of arylsulfatase B gene mutations and clinical presentations of Iranian patients with Mucopolysaccharidosis VI.
Majid Aminzadeh, Nasrin Malekpour, Pegah Ghandil

Gene· July 2019

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Childhood onset type 1 diabetes at a tertiary hospital in south-western Iran during 2000-2015: Rapid increase in admissions and high prevalence of DKA at diagnosis.
Majid Aminzadeh, Najmeh Navidi, Ehsan Valavi, Seyyed Mohammad Hassan Aletayeb

Prim Care Diabetes· February 2019

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Higher prevalence of permanent congenital hypothyroidism in the Southwest of Iran mostly caused by dyshormonogenesis: a five-year follow-up study.
Majid Aminzadeh

Arch Endocrinol Metab· February 2019

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Niemann-Pick Diseases: The Largest Iranian Cohort with Genetic Analysis.
Somayyeh Hashemian, Peyman Eshraghi, Nafi Dilaver, Hamid Galehdari, Bita Shalbafan, Majid Aminzadeh

Iran J Child Neurol· January 2019

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Vitamin D status in diabetic children and adolescents.
Tahereh Ziaei-Kajbaf, Majid Aminzadeh, Elham Fatahinezhad, Seyyed Mohammad-Hassan Aletayeb

Diabetes Metab Syndr· November 2018

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Identification of a novel mutation in ARSA gene in three patients of an Iranian family with metachromatic leukodystrophy disorder.
Neda Golchin, Mohammadreza Hajjari, Reza Azizi Malamiri, Majid Aminzadeh, Javad Mohammadi-Asl

Genet Mol Biol· November 2017

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Comparison between maternal and neonatal serum vitamin D levels in term jaundiced and nonjaundiced cases.
Seyyed Mohammad Hassan Aletayeb, Masoud Dehdashtiyan, Majid Aminzadeh, Arash Malekyan, Somayeh Jafrasteh

J Chin Med Assoc· November 2016

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Neck Circumference as a Useful Marker for Screening Overweight and Obesity in Children and Adolescents.
Mehri Taheri, Tahereh Ziaei Kajbaf, Mohammad-Reza Taheri, Majid Aminzadeh

Oman Med J· May 2016

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Molecular determination of glutaric aciduria type I in individuals from southwest Iran.
Masumeh Baradaran, Hamid Galehdari, Majid Aminzadeh, Reza Azizi Malmiri, Raheleh Tangestani

Arch Iran Med· September 2014

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