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Nanoscale
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July 21, 2017
Spin-reversal energy barriers of 305 K for Fe<sup>2+</sup> d<sup>6</sup> ions with linear ligand coordination
Lei Xu, Ziba Zangeneh, Ravi Yadav, et al.
Journal of Movement Disorders
|
March 27, 2024
Knowledge, Attitudes and Perceptions of Genetic Testing Among Patients With Movement Disorders, Their Caregivers and Health Care Professionals
Sneha D Kamath, Vikram V Holla, Nitish Kamble, et al.
Journal of Movement Disorders
|
February 22, 2026
Potassium calcium-activated Channel subfamily M Alpha1 (KCNMA1) Channelopathy: First case report from India
M K Farsana, Vikram V Holla, Mit Ankur Raval, et al.
Parkinsonism & Related Disorders
|
January 14, 2024
Clinical and genetic profile of patients with dystonia: An experience from a tertiary neurology center from India
Debjyoti Dhar, Vikram V Holla, Riyanka Kumari, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
August 20, 2016
Is pruritus an indicator of aquaporin-positive neuromyelitis optica?
Manjunath Netravathi, Jitender Saini, Anita Mahadevan, et al.
Scientific Reports
|
December 1, 2016
Kitaev exchange and field-induced quantum spin-liquid states in honeycomb α-RuCl<sub>3</sub>
Ravi Yadav, Nikolay A Bogdanov, Vamshi M Katukuri, et al.
Chemical Communications (Cambridge, England)
|
December 17, 2021
Triple-decker complexes incorporating three distinct deck architectures
Xiaofei Sun, Akhil Kumar Singh, Ravi Yadav, et al.
Journal of Geriatric Psychiatry and Neurology
|
May 17, 2022
Prevalence and Correlates of Psychiatric Comorbidity and Multimorbidity in Parkinson's Disease and Atypical Parkinsonian Syndromes
Vinit Patel, Jaisoorya Ts, Nitish Kamble, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
January 10, 2024
Sexual dysfunction in men with young onset Parkinson's disease
M Sandeep, Shyam Sundar, Vikram V Holla, et al.
Journal of Human Genetics
|
September 26, 2023
Novel CWF19L1 mutations in patients with spinocerebellar ataxia, autosomal recessive 17
Prashant Phulpagar, Vikram V Holla, Deepti Tomar, et al.
Page
of 43
Search research articles
Search
Showing results (201-210 of 430) with videos related to
Sort By:
Page
of 43
Nanoscale
|
July 21, 2017
Spin-reversal energy barriers of 305 K for Fe<sup>2+</sup> d<sup>6</sup> ions with linear ligand coordination
Lei Xu, Ziba Zangeneh, Ravi Yadav, et al.
Journal of Movement Disorders
|
March 27, 2024
Knowledge, Attitudes and Perceptions of Genetic Testing Among Patients With Movement Disorders, Their Caregivers and Health Care Professionals
Sneha D Kamath, Vikram V Holla, Nitish Kamble, et al.
Journal of Movement Disorders
|
February 22, 2026
Potassium calcium-activated Channel subfamily M Alpha1 (KCNMA1) Channelopathy: First case report from India
M K Farsana, Vikram V Holla, Mit Ankur Raval, et al.
Parkinsonism & Related Disorders
|
January 14, 2024
Clinical and genetic profile of patients with dystonia: An experience from a tertiary neurology center from India
Debjyoti Dhar, Vikram V Holla, Riyanka Kumari, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
August 20, 2016
Is pruritus an indicator of aquaporin-positive neuromyelitis optica?
Manjunath Netravathi, Jitender Saini, Anita Mahadevan, et al.
Scientific Reports
|
December 1, 2016
Kitaev exchange and field-induced quantum spin-liquid states in honeycomb α-RuCl<sub>3</sub>
Ravi Yadav, Nikolay A Bogdanov, Vamshi M Katukuri, et al.
Chemical Communications (Cambridge, England)
|
December 17, 2021
Triple-decker complexes incorporating three distinct deck architectures
Xiaofei Sun, Akhil Kumar Singh, Ravi Yadav, et al.
Journal of Geriatric Psychiatry and Neurology
|
May 17, 2022
Prevalence and Correlates of Psychiatric Comorbidity and Multimorbidity in Parkinson's Disease and Atypical Parkinsonian Syndromes
Vinit Patel, Jaisoorya Ts, Nitish Kamble, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
January 10, 2024
Sexual dysfunction in men with young onset Parkinson's disease
M Sandeep, Shyam Sundar, Vikram V Holla, et al.
Journal of Human Genetics
|
September 26, 2023
Novel CWF19L1 mutations in patients with spinocerebellar ataxia, autosomal recessive 17
Prashant Phulpagar, Vikram V Holla, Deepti Tomar, et al.
Page
of 43