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Parkinsonism & Related Disorders
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November 3, 2023
Looking beyond the brain: Insights into vascular parkinsonism with optical coherence tomography
Aakash Agrawal, Pooja Mailankody, Rajani Battu, et al.
Annals of Indian Academy of Neurology
|
June 5, 2024
OPA1 Mutation Presenting as Ethambutol-Induced Optic Neuropathy
Agam Jain, Saraswati Nashi, Pooja Mailankody, et al.
Annals of Indian Academy of Neurology
|
March 9, 2026
Multiphasic Infarcts in a Young Brain Secondary to Thrombotic Thrombocytopenic Purpura: Looking Beyond the Usual Suspects
N Javagal A Thejas, Arka P Chattopadhyay, Raghavendra Kenchiah, et al.
The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry
|
April 18, 2023
A systematic review and meta-analysis of optical coherence tomography studies in schizophrenia, bipolar disorder and major depressive disorder
Akash Prasannakumar, Vijay Kumar, Pooja Mailankody, et al.
Annals of Indian Academy of Neurology
|
April 1, 2022
Parkinsonism, Olivary Hypertrophy and Cerebellar Atrophy with <i>TTC19</i> Gene Mutation
Rohan R Mahale, Gautham Arunachal, Jyothi Gautam, et al.
Neurology India
|
March 5, 2020
Blink Reflex is Significantly Altered in Patients with Multisystem Atrophy Compared to Patients with Progressive Supranuclear Palsy, Alzheimer's Disease, and Frontotemporal Dementia ‑ A Pilot Study
Sadanandavalli R Chandra, Nitin C Ramanujam, Abhishek Gohel, et al.
Annals of Indian Academy of Neurology
|
June 13, 2022
Pseudo-neonatal Adrenoleukodystrophy: A Rare Peroxisomal Disorder
Cheshta Arora, Hansashree Padmanabha, Rita Christopher, et al.
Journal of Pediatric Neurosciences
|
January 12, 2022
Rapidly Progressive Spastic Paraplegia Due to Hyperhomocysteinemia in Child with <i>MTHFR</i> Gene Mutation and Mitochondrial Complex I Deficiency: A Rare Association
Rohan R Mahale, Jyothi Gautam, Gautam Arunachal, et al.
Acta Neurologica Belgica
|
July 3, 2021
Stroke-like episodes with cerebellar ataxia as presenting manifestation of adult-onset anti-N-methyl D-aspartate receptor encephalitis: an unusual presentation
Rohan Mahale, M K Farsana, Anitha Mahadevan, et al.
Neurology India
|
September 14, 2025
The Treatment Profile of Migraine in India: A Glimpse of the Real World Scenario
Avinash Kumar, Gs Shubha Bhat, Durai Murukan Gunasekaran, et al.
Page
of 11
Search research articles
Search
Showing results (61-70 of 103) with videos related to
Sort By:
Page
of 11
Parkinsonism & Related Disorders
|
November 3, 2023
Looking beyond the brain: Insights into vascular parkinsonism with optical coherence tomography
Aakash Agrawal, Pooja Mailankody, Rajani Battu, et al.
Annals of Indian Academy of Neurology
|
June 5, 2024
OPA1 Mutation Presenting as Ethambutol-Induced Optic Neuropathy
Agam Jain, Saraswati Nashi, Pooja Mailankody, et al.
Annals of Indian Academy of Neurology
|
March 9, 2026
Multiphasic Infarcts in a Young Brain Secondary to Thrombotic Thrombocytopenic Purpura: Looking Beyond the Usual Suspects
N Javagal A Thejas, Arka P Chattopadhyay, Raghavendra Kenchiah, et al.
The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry
|
April 18, 2023
A systematic review and meta-analysis of optical coherence tomography studies in schizophrenia, bipolar disorder and major depressive disorder
Akash Prasannakumar, Vijay Kumar, Pooja Mailankody, et al.
Annals of Indian Academy of Neurology
|
April 1, 2022
Parkinsonism, Olivary Hypertrophy and Cerebellar Atrophy with <i>TTC19</i> Gene Mutation
Rohan R Mahale, Gautham Arunachal, Jyothi Gautam, et al.
Neurology India
|
March 5, 2020
Blink Reflex is Significantly Altered in Patients with Multisystem Atrophy Compared to Patients with Progressive Supranuclear Palsy, Alzheimer's Disease, and Frontotemporal Dementia ‑ A Pilot Study
Sadanandavalli R Chandra, Nitin C Ramanujam, Abhishek Gohel, et al.
Annals of Indian Academy of Neurology
|
June 13, 2022
Pseudo-neonatal Adrenoleukodystrophy: A Rare Peroxisomal Disorder
Cheshta Arora, Hansashree Padmanabha, Rita Christopher, et al.
Journal of Pediatric Neurosciences
|
January 12, 2022
Rapidly Progressive Spastic Paraplegia Due to Hyperhomocysteinemia in Child with <i>MTHFR</i> Gene Mutation and Mitochondrial Complex I Deficiency: A Rare Association
Rohan R Mahale, Jyothi Gautam, Gautam Arunachal, et al.
Acta Neurologica Belgica
|
July 3, 2021
Stroke-like episodes with cerebellar ataxia as presenting manifestation of adult-onset anti-N-methyl D-aspartate receptor encephalitis: an unusual presentation
Rohan Mahale, M K Farsana, Anitha Mahadevan, et al.
Neurology India
|
September 14, 2025
The Treatment Profile of Migraine in India: A Glimpse of the Real World Scenario
Avinash Kumar, Gs Shubha Bhat, Durai Murukan Gunasekaran, et al.
Page
of 11