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Acta Neurologica Belgica
|
January 23, 2021
Isolated mitochondrial myopathy due to m.3243A > G mutation in MT-TL1 gene
Rohan R Mahale, Jyothi Gautham, Pooja Mailankody, et al.
Annals of Indian Academy of Neurology
|
March 7, 2015
Episodic neurological dysfunction in hereditary peripheral neuropathy
Girish Baburao Kulkarni, Pooja Mailankody, Pawanraj Palu Isnwara, et al.
Journal of the Neurological Sciences
|
June 12, 2016
Re-emergent tremor in Parkinson's disease: A clinical and electromyographic study
Pooja Mailankody, K Thennarasu, B C Nagaraju, et al.
Annals of Neurosciences
|
June 8, 2026
Retinal Architecture in Parkinson's Disease with Rapid Eye Movement Sleep Behaviour Disorder: Insights from a Scoping Review
Megha Shri Nanjundaswamy, Pooja Mailankody, Monojit Debnath, et al.
Parkinsonism & Related Disorders
|
August 23, 2015
Optical coherence tomography as a tool to evaluate retinal changes in Parkinson's disease
Pooja Mailankody, Rajani Battu, Anjani Khanna, et al.
Acta Neurologica Belgica
|
March 29, 2022
Anti-GAD antibodies associated autoimmunity presenting as isolated dementia: an expansion of GAD antibody-spectrum disorders
Rohan R Mahale, Srinath Rajeevan, S Sivaprakash, et al.
Journal of Paediatrics and Child Health
|
February 12, 2020
'All that waddles is not dystrophy'
Hansashree Padmanabha, Sadanandavalli R Chandra, Annapureddy Jagadish, et al.
Parkinsonism & Related Disorders
|
October 2, 2023
Cortical excitability changes in patients of vascular parkinsonism with cognitive impairment
Aakash Agrawal, Amitabh Bhattacharya, Nitish Kamble, et al.
Annals of Indian Academy of Neurology
|
August 8, 2022
Levodopa Non-Responsive Parkinsonism in Tuberculous Cerebral Arteritis: A Rare Occurrence
Rohan Mahale, Arun Gokul Pon, M Sandeep, et al.
Journal of Pediatric Neurosciences
|
February 3, 2021
A Rare Case of Ataxia-Telangiectasia-Like Disorder With <i>MRE11</i> Mutation
Rohan R Mahale, Nishanth Reddy, Pavagada Mathuranth, et al.
Page
of 11
Search research articles
Search
Showing results (31-40 of 103) with videos related to
Sort By:
Page
of 11
Acta Neurologica Belgica
|
January 23, 2021
Isolated mitochondrial myopathy due to m.3243A > G mutation in MT-TL1 gene
Rohan R Mahale, Jyothi Gautham, Pooja Mailankody, et al.
Annals of Indian Academy of Neurology
|
March 7, 2015
Episodic neurological dysfunction in hereditary peripheral neuropathy
Girish Baburao Kulkarni, Pooja Mailankody, Pawanraj Palu Isnwara, et al.
Journal of the Neurological Sciences
|
June 12, 2016
Re-emergent tremor in Parkinson's disease: A clinical and electromyographic study
Pooja Mailankody, K Thennarasu, B C Nagaraju, et al.
Annals of Neurosciences
|
June 8, 2026
Retinal Architecture in Parkinson's Disease with Rapid Eye Movement Sleep Behaviour Disorder: Insights from a Scoping Review
Megha Shri Nanjundaswamy, Pooja Mailankody, Monojit Debnath, et al.
Parkinsonism & Related Disorders
|
August 23, 2015
Optical coherence tomography as a tool to evaluate retinal changes in Parkinson's disease
Pooja Mailankody, Rajani Battu, Anjani Khanna, et al.
Acta Neurologica Belgica
|
March 29, 2022
Anti-GAD antibodies associated autoimmunity presenting as isolated dementia: an expansion of GAD antibody-spectrum disorders
Rohan R Mahale, Srinath Rajeevan, S Sivaprakash, et al.
Journal of Paediatrics and Child Health
|
February 12, 2020
'All that waddles is not dystrophy'
Hansashree Padmanabha, Sadanandavalli R Chandra, Annapureddy Jagadish, et al.
Parkinsonism & Related Disorders
|
October 2, 2023
Cortical excitability changes in patients of vascular parkinsonism with cognitive impairment
Aakash Agrawal, Amitabh Bhattacharya, Nitish Kamble, et al.
Annals of Indian Academy of Neurology
|
August 8, 2022
Levodopa Non-Responsive Parkinsonism in Tuberculous Cerebral Arteritis: A Rare Occurrence
Rohan Mahale, Arun Gokul Pon, M Sandeep, et al.
Journal of Pediatric Neurosciences
|
February 3, 2021
A Rare Case of Ataxia-Telangiectasia-Like Disorder With <i>MRE11</i> Mutation
Rohan R Mahale, Nishanth Reddy, Pavagada Mathuranth, et al.
Page
of 11