Gautham Arunachal

Hosur Road
Bengaluru, KA 560029, India

Last Updated: 09/26/2026

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Found 110 publications

Molecular characterization of individuals with RASopathies: Spectrum of genetic variants in a large Indian cohort.

Molecular characterization of individuals with RASopathies: Spectrum of genetic variants in a large Indian cohort.

Journal: Journal of genetics

Published: June 11, 2026

Genome-wide spectrum of coding DNA variations in Indian patients with amyotrophic lateral sclerosis.

Genome-wide spectrum of coding DNA variations in Indian patients with amyotrophic lateral sclerosis.

Journal: Journal of neurology

Published: January 28, 2026

When Benign Isn't So Benign: "Status Choreatus" in Benign Hereditary Chorea Challenging the Norm.

When Benign Isn't So Benign: "Status Choreatus" in Benign Hereditary Chorea Challenging the Norm.

Journal: Movement disorders clinical practice

Published: January 11, 2026

Clinical trajectories and genetic profiles of SOD1-related amyotrophic lateral sclerosis: insights from a single-center cohort in India.

Clinical trajectories and genetic profiles of SOD1-related amyotrophic lateral sclerosis: insights from a single-center cohort in India.

Journal: Journal of neurology

Published: November 10, 2025

Plasma Glial Fibrillary Acidic Protein (GFAP) shows age-dependent associations with externalizing psychopathology and atypical brain connectivity.

Plasma Glial Fibrillary Acidic Protein (GFAP) shows age-dependent associations with externalizing psychopathology and atypical brain connectivity.

Journal: Translational psychiatry

Published: October 04, 2025

KCTD7-related progressive myoclonic epilepsy: Clinical and genetic characterization of six Indian patients and review of literature.

KCTD7-related progressive myoclonic epilepsy: Clinical and genetic characterization of six Indian patients and review of literature.

Journal: Seizure

Published: October 03, 2025

An interesting report of POPDC3 limb girdle muscular dystrophy R26 from India.

An interesting report of POPDC3 limb girdle muscular dystrophy R26 from India.

Journal: Journal of neuromuscular diseases

Published: September 30, 2025

SPTBN2- associated early-onset Parkinson's disease: A phenotypic expansion.

SPTBN2- associated early-onset Parkinson's disease: A phenotypic expansion.

Journal: Parkinsonism & related disorders

Published: July 22, 2025

An atypical case of FA2H-related HSP35 with subtle neuroimaging findings and a novel variant in a young adult with spastic paraparesis.

An atypical case of FA2H-related HSP35 with subtle neuroimaging findings and a novel variant in a young adult with spastic paraparesis.

Journal: Acta neurologica Belgica

Published: July 16, 2025

Novel muscle MRI features in Desmin related myasthenic myopathy.

Novel muscle MRI features in Desmin related myasthenic myopathy.

Journal: Neuromuscular disorders : NMD

Published: July 06, 2025

Myofibrillar Myopathy: Clinico-Genetic Spectrum From a Neuromuscular Center in South India.

Myofibrillar Myopathy: Clinico-Genetic Spectrum From a Neuromuscular Center in South India.

Journal: Journal of clinical neuromuscular disease

Published: June 13, 2025

Acute refractory chorea as a novel phenotype of NARS2 gene mutation-related mitochondrial disorder.

Acute refractory chorea as a novel phenotype of NARS2 gene mutation-related mitochondrial disorder.

Journal: Parkinsonism & related disorders

Published: May 30, 2025

Showing 1-12 of 110

Last Updated: 09/26/2026