Rohan R. Mahale-Rohan

Hosur Road
Bengaluru, KA 560029, India

Last Updated: 09/26/2026

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Found 35 publications

THG1L- associated early childhood-onset cerebellar ataxia with atrophy and developmental delay.

THG1L- associated early childhood-onset cerebellar ataxia with atrophy and developmental delay.

Journal: Neurogenetics
Published: June 24, 2026

FAT2-associated early-onset cerebellar ataxia: report of novel phenotype and variant.

FAT2-associated early-onset cerebellar ataxia: report of novel phenotype and variant.

Journal: Acta neurologica Belgica
Published: June 02, 2026

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

Hypogonadotrophic hypogonadism in GBA2 associated spastic paraplegia type 46 (SPG46): a phenotypic expansion.

Hypogonadotrophic hypogonadism in GBA2 associated spastic paraplegia type 46 (SPG46): a phenotypic expansion.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: February 11, 2026

Deep brain stimulation beyond Motor control: A systematic review and meta-analysis of sleep outcomes in Parkinson's disease.

Deep brain stimulation beyond Motor control: A systematic review and meta-analysis of sleep outcomes in Parkinson's disease.

Journal: Parkinsonism & related disorders
Published: December 18, 2025

Late-onset cerebellar ataxia associated with XRCC1: Expanding the phenotypic spectrum.

Late-onset cerebellar ataxia associated with XRCC1: Expanding the phenotypic spectrum.

Journal: Parkinsonism & related disorders
Published: November 18, 2025

Clinical and Genetic Profile of Gordon-Holmes Syndrome: A Review of Published Cases : Original Article.

Clinical and Genetic Profile of Gordon-Holmes Syndrome: A Review of Published Cases : Original Article.

Journal: Cerebellum (London, England)
Published: October 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

CSF1R-related disorder: A clinical, imaging and genetic profile review.

CSF1R-related disorder: A clinical, imaging and genetic profile review.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: January 24, 2025

Non-motor fluctuations in Parkinson's disease: frequency and clinical correlate.

Non-motor fluctuations in Parkinson's disease: frequency and clinical correlate.

Journal: Journal of neural transmission (Vienna, Austria : 1996)
Published: January 15, 2025

Cerebral abscesses due to Pseudallescheria boydii mycoses: a diagnostic and therapeutic conundrum.

Cerebral abscesses due to Pseudallescheria boydii mycoses: a diagnostic and therapeutic conundrum.

Journal: Acta neurologica Belgica
Published: September 16, 2024
Showing 1-12 of 35

Last Updated: 09/26/2026