Hamid Galehdari

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 9

Top Topics

Genome Wide Association

Botulinum Toxin

Top Venues

Brain : a journal of neurology

Basic and clinical neuroscience

Molecular genetics & genomic medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Raffaella De Pace, Reza Maroofian, Adeline Paimboeuf, Mina Zamani, Maha Saad Zaki, Saeid Sadeghian, Reza Azizimalamiri, Hamid Galehdari, Jawaher Zeighami, Chad D Williamson, Emily Fleming, Dihong Zhou, Jennifer L Gannon, Isabelle Thiffault, Emmanuel Roze, Mohnish Suri, Giovanni Zifarelli, Peter Bauer, Henry Houlden, Mariasavina Severino, Shunmoogum A Patten, Emily G Farrow, Juan S Bonifacino
Biallelic BORCS8 variants cause an infantile-onset neurodegenerative disorder with altered lysosome dynamics. Brain : a journal of neurology 147 (5) (2024)
Raffaella De Pace, Reza Maroofian, Adeline Paimboeuf, Mina Zamani, Maha Saad Zaki, Saeid Sadeghian, Reza Azizimalamiri, Hamid Galehdari, Jawaher Zeighami, Chad D Williamson, Emily Fleming, Dihong Zhou, Jennifer L Gannon, Isabelle Thiffault, Emmanuel Roze, Mohnish Suri, Giovanni Zifarelli, Peter Bauer, Henry Houlden, Mariasavina Severino, Shunmoogum A Patten, Emily G Farrow, Juan S Bonifacino
Biallelic BORCS8 variants cause an infantile-onset neurodegenerative disorder with altered lysosome dynamics. Brain : a journal of neurology 147 (5) (2024)
Raffaella De Pace, Reza Maroofian, Adeline Paimboeuf, Mina Zamani, Maha Saad Zaki, Saeid Sadeghian, Reza Azizimalamiri, Hamid Galehdari, Jawaher Zeighami, Chad D Williamson, Emily Fleming, Dihong Zhou, Jennifer L Gannon, Isabelle Thiffault, Emmanuel Roze, Mohnish Suri, Giovanni Zifarelli, Peter Bauer, Henry Houlden, Mariasavina Severino, Shunmoogum A Patten, Emily G Farrow, Juan S Bonifacino
Biallelic BORCS8 variants cause an infantile-onset neurodegenerative disorder with altered lysosome dynamics. Brain : a journal of neurology 147 (5) (2024)
Seyed Reza Kazemi Nezhad, Pegah Namdar Aligoodarzi, Golale Rostami, Gholamreza Shariati, Hamid Galehdari, Alihossein Saberi, Alireza Sedaghat, Mohammad Hamid
Genotypic variants of the tetrahydrobiopterin (BH4) biosynthesis genes in patients with hyperphenylalaninemia from different regions of Iran. Molecular genetics & genomic medicine (2023)
Fatemeh Yaghoobizadeh, Mohammad Roayaei Ardakani, Mohammad Mehdi Ranjbar, Mohammad Khosravi, Hamid Galehdari
Preparation, Purification and Performance Evaluation of Polyclonal Antibody Against SARS-CoV-2 Produced in Rat. Advanced pharmaceutical bulletin 13 (3) (2022)
Negar Noorbakhsh, Hamid Galehdari, Mohammad Shafiei
The Effect of Sialic Acid on MiR-320a and Let-7e Expression in Human Glial Cell Line. Basic and clinical neuroscience 13 (3) (2022)
Mina Zamani, Sahar Sedighzadeh, Tahereh Seifi, Samira Negahdari, Jawaher Zeighami, Alireza Sedaghat, Gholamreza Shariati, Hamid Galehdari
Whole-exome sequencing deciphers the genetic profile of visual impairments in patients from Southwest Iran. Molecular genetics and genomics : MGG 297 (5) (2022)
Mina Zamani, Tahereh Seifi, Sahar Sedighzadeh, Samira Negahdari, Jawaher Zeighami, Alireza Sedaghat, Tahereh Yadegari, Alihossein Saberi, Mohammad Hamid, Gholamreza Shariati, Hamid Galehdari
Whole-Exome Sequencing Application for Genetic Diagnosis of Kidney Diseases: A Study from Southwest of Iran. Kidney360 2 (5) (2021)
Mina Zamani, Tahereh Seifi, Jawaher Zeighami, Neda Mazaheri, Emad Jahangirnezhad, Minoo Gholamzadeh, Alireza Sedaghat, Gholamreza Shariati, Hamid Galehdari
Identification of the rs797045105 in the SERAC1 Gene by Whole-exome Sequencing in a Patient Suspicious of MEGDEL Syndrome. Basic and clinical neuroscience 11 (4) (2020)