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Pooja Mailankody

Showing results (11-20 of 102) with videos related to

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Acta Neurologica Belgica|November 17, 2023
Late-onset spastic-ataxia due to KIF1C mutation: broadening the SPG 58 phenotypeRohan Mahale, Hansashree Padmanabha, Pooja Mailankody, et al.
Parkinsonism & Related Disorders|September 28, 2025
SPTBN2- associated early-onset Parkinson's disease: A phenotypic expansionRohan Mahale, Gautham Arunachal, Hansashree Padmanabha, et al.
Parkinsonism & Related Disorders|October 9, 2024
Adult-onset cranio-cervical segmental dystonia due to ADAR1 gene mutation: A novel phenotypeRohan Mahale, Gautham Arunachal, Hansashree Padmanabha, et al.
Annals of Indian Academy of Neurology|January 10, 2022
Kennedy's Disease: A Second Genetically Confirmed Report from IndiaRutul Shah, Rohan Mahale, Hansashree Padmanabha, et al.
Neurology India|November 8, 2021
The Rationale of Yoga in Parkinson's Disease: A Critical ReviewPooja Mailankody, Shivarama Varambally, K Thennarasu, et al.
Neurology India|June 16, 2023
Yoga in Parkinson's Disease: Movement from Disorder to OrderPooja Mailankody, Shivarama Varambally, K Thennarasu, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 1, 2026
Hypogonadotrophic hypogonadism in GBA2 associated spastic paraplegia type 46 (SPG46): a phenotypic expansionRohan R Mahale, Pramod Khanda, Sushmita Upadhyay, et al.
Annals of Indian Academy of Neurology|August 8, 2022
Vascular Parkinsonism with Dystonia in Moyamoya Disease: An Expansion of Movement Disorder PhenomenologyRohan R Mahale, Rohin Dubbal, Hansashree Padmanabha, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|April 2, 2026
Clinical, imaging and genetic profile of KMT2B-related dystonia: a review of published casesRohan R Mahale, Pramod Khanda, Subhajit Roy, et al.
Parkinsonism & Related Disorders|June 27, 2021
DNAJC6 mutation causing cranial-onset dystonia with tremor dominant levodopa non-responsive parkinsonism: A novel phenotypeSomdattaa Ray, Hansashree Padmanabha, Rohan Mahale, et al.
Pageof 11

Showing results (11-20 of 102) with videos related to

Sort By:
Pageof 11
Acta Neurologica Belgica|November 17, 2023
Late-onset spastic-ataxia due to KIF1C mutation: broadening the SPG 58 phenotypeRohan Mahale, Hansashree Padmanabha, Pooja Mailankody, et al.
Parkinsonism & Related Disorders|September 28, 2025
SPTBN2- associated early-onset Parkinson's disease: A phenotypic expansionRohan Mahale, Gautham Arunachal, Hansashree Padmanabha, et al.
Parkinsonism & Related Disorders|October 9, 2024
Adult-onset cranio-cervical segmental dystonia due to ADAR1 gene mutation: A novel phenotypeRohan Mahale, Gautham Arunachal, Hansashree Padmanabha, et al.
Annals of Indian Academy of Neurology|January 10, 2022
Kennedy's Disease: A Second Genetically Confirmed Report from IndiaRutul Shah, Rohan Mahale, Hansashree Padmanabha, et al.
Neurology India|November 8, 2021
The Rationale of Yoga in Parkinson's Disease: A Critical ReviewPooja Mailankody, Shivarama Varambally, K Thennarasu, et al.
Neurology India|June 16, 2023
Yoga in Parkinson's Disease: Movement from Disorder to OrderPooja Mailankody, Shivarama Varambally, K Thennarasu, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 1, 2026
Hypogonadotrophic hypogonadism in GBA2 associated spastic paraplegia type 46 (SPG46): a phenotypic expansionRohan R Mahale, Pramod Khanda, Sushmita Upadhyay, et al.
Annals of Indian Academy of Neurology|August 8, 2022
Vascular Parkinsonism with Dystonia in Moyamoya Disease: An Expansion of Movement Disorder PhenomenologyRohan R Mahale, Rohin Dubbal, Hansashree Padmanabha, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|April 2, 2026
Clinical, imaging and genetic profile of KMT2B-related dystonia: a review of published casesRohan R Mahale, Pramod Khanda, Subhajit Roy, et al.
Parkinsonism & Related Disorders|June 27, 2021
DNAJC6 mutation causing cranial-onset dystonia with tremor dominant levodopa non-responsive parkinsonism: A novel phenotypeSomdattaa Ray, Hansashree Padmanabha, Rohan Mahale, et al.
Pageof 11