Subhajit Roy

Hosur Road
Bengaluru, KA 560029, India

Last Updated: 09/26/2026

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Found 10 publications

FBXO7- associated parkinsonism: clinical, genetic, and radiological insights from a case report and literature review.

FBXO7- associated parkinsonism: clinical, genetic, and radiological insights from a case report and literature review.

Journal: Journal of neural transmission (Vienna, Austria : 1996)

Published: May 28, 2026

Clinical, imaging and genetic profile of KMT2B-related dystonia: a review of published cases.

Clinical, imaging and genetic profile of KMT2B-related dystonia: a review of published cases.

Journal: Journal of neural transmission (Vienna, Austria : 1996)

Published: February 24, 2026

Alternating hemispheric focal status epilepticus : An atypical presentation of genetically confirmed case of MERRF syndrome.

Alternating hemispheric focal status epilepticus : An atypical presentation of genetically confirmed case of MERRF syndrome.

Journal: Seizure

Published: February 10, 2026

Adult-onset DNAJB4-related limb-girdle myopathy-expanding the phenotypic spectrum.

Adult-onset DNAJB4-related limb-girdle myopathy-expanding the phenotypic spectrum.

Journal: Acta neurologica Belgica

Published: January 01, 2026

Clinical, Radiological, and Genetic Profiles of Eight Patients with Combined Dystonic Manifestation of Type-III GM1 Gangliosidosis: A Video Case Series from India.

Clinical, Radiological, and Genetic Profiles of Eight Patients with Combined Dystonic Manifestation of Type-III GM1 Gangliosidosis: A Video Case Series from India.

Journal: Tremor and other hyperkinetic movements (New York, N.Y.)

Published: December 08, 2025

CLCN2-Related Leukoencephalopathy Presenting as Isolated Paroxysmal Non-Kinesigenic Dyskinesia: Clinical, Imaging, and Genetic Correlations.

CLCN2-Related Leukoencephalopathy Presenting as Isolated Paroxysmal Non-Kinesigenic Dyskinesia: Clinical, Imaging, and Genetic Correlations.

Journal: Journal of movement disorders

Published: October 05, 2025

The herculean illusion: congenital hypothyroidism masquerading as muscular dystrophy.

The herculean illusion: congenital hypothyroidism masquerading as muscular dystrophy.

Journal: Acta neurologica Belgica

Published: October 02, 2025

Kufor-Rakeb syndrome: a cohort-based clinical, imaging and genetic profile.

Kufor-Rakeb syndrome: a cohort-based clinical, imaging and genetic profile.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: August 27, 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

Clinico-investigational profile, relapse predictors and outcomes of pediatric patients with anti-myelin oligodendrocyte associated disorders: An experience from tertiary centre.

Clinico-investigational profile, relapse predictors and outcomes of pediatric patients with anti-myelin oligodendrocyte associated disorders: An experience from tertiary centre.

Journal: Multiple sclerosis and related disorders

Published: September 30, 2024

Showing 1-10 of 10

Last Updated: 09/26/2026