Mohd Faruq
Mall Road
Delhi, DL 110007, India
Delhi, DL 110007, India
Last Updated: 09/26/2026
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Found 15 publications
Dominant Mutation in ITPR3 Gene Causing Charcot-Marie-Tooth Disease 1J in a Family from India.
Journal: Annals of Indian Academy of Neurology
Published: November 14, 2023
"Ear of the Lynx" Sign in Hereditary Spastic Paraparesis (HSP) 76.
Journal: Movement disorders clinical practice
Published: August 18, 2022
Human-host transcriptomic analysis reveals unique early innate immune responses in different sub-phenotypes of COVID-19.
Journal: Clinical and translational medicine
Published: January 25, 2022
Cognition in Trinucleotide Repeat Spinocerebellar Ataxias: A Review.
Journal: Annals of Indian Academy of Neurology
Published: January 18, 2022
Genetic Testing in Neurology: What Every Neurologist Must Know.
Journal: Annals of Indian Academy of Neurology
Published: September 24, 2021
Allgrove Syndrome: A Frequently Under-Diagnosed ALS Mimic.
Journal: Annals of Indian Academy of Neurology
Published: June 28, 2021
SCA2 in the Indian population: Unified haplotype and variable phenotypic patterns in a large case series.
Journal: Parkinsonism & related disorders
Published: April 17, 2021
Investigations of Huntington's Disease and Huntington's Disease-Like Syndromes in Indian Choreatic Patients.
Journal: Journal of Huntington's disease
Published: July 18, 2020
Generation of three spinocerebellar ataxia type-12 patients derived induced pluripotent stem cell lines (IGIBi002-A, IGIBi003-A and IGIBi004-A).
Journal: Stem cell research
Published: June 19, 2018
Iron related hemochromatosis (HFE) gene mutations in Friedreich Ataxia patients.
Journal: Parkinsonism & related disorders
Published: April 12, 2016
Last Updated: 09/26/2026