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Journal of Genetics|April 19, 2018
Genetic testing for clinically suspected spinocerebellar ataxias: report from a tertiary referral centre in IndiaSowmya Devatha Venkatesh, Mahesh Kandasamy, Nagaraj S Moily, et al.
European Journal of Human Genetics : EJHG|January 4, 2025
C19orf12 gene variants causing mitochondrial membrane protein-associated neurodegeneration (MPAN)Riyanka Kumari, Vikram V Holla, Neeharika Sriram, et al.
Journal of Family Medicine and Primary Care|November 10, 2022
CoRe study: COVID-19 and remdesivir: An insight into the current health planning and policyM M Samim, Debjyoti Dhar, Vikram Singh, et al.
Journal of Neuroendocrinology|July 25, 2022
Whole exome sequencing and transcript analysis discover a novel pathogenic splice site mutation in DCAF17 gene underlying Woodhouse-Sakati syndromeRiyanka Kumari, Vikram V Holla, Prashant Phulpagar, et al.
World Neurosurgery|December 7, 2020
Cervical Myeloradiculopathy and Atlantoaxial Instability in Cervical DystoniaKoti Neeraja, Shweta Prasad, Bharath Kumar Surisetti, et al.
Movement Disorders Clinical Practice|October 27, 2018
Role of Corpus Callosum Volumetry in Differentiating the Subtypes of Progressive Supranuclear Palsy and Early Parkinson's DiseaseAbhishek Lenka, Shaik Afsar Pasha, Sandhya Mangalore, et al.
Parkinsonism & Related Disorders|May 5, 2024
Definition, diagnosis and classification of infection-related movement disorders: Consensus proposalSoaham Desai, Norlinah Mohamed Ibrahim, Divyani Garg, et al.
Journal of Huntington'S Disease|December 20, 2015
Determinants of Onset of Huntington's Disease with Behavioral Symptoms: Insight from 92 PatientsAbhishek Lenka, Nitish L Kamble, V Sowmya, et al.
Scientific Reports|April 1, 2025
Source-specific fine particulates emission linked to prevalence of ophthalmic cases in IndiaSaroj Kumar Sahu, Ashirbad Mishra, Poonam Mangaraj, et al.
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