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Annals of Indian Academy of Neurology
|
March 18, 2024
Association of Insulin-like Growth Factor-1 and Neurofilament Light Chain in Patients with Progressive Supranuclear Palsy
Saikat Dey, Ramachadra Yelamanchi, Thrinath Mullapudi, et al.
Plos One
|
September 12, 2025
Virulence gene profile and antimicrobial resistance patterns of Aeromonas hydrophila in farmed catfishes (Heteropneustes fossilis and Pangasianodon hypophthalmus) for the first time in Bangladesh
Farjana Ferdousi, Bushra Benta Rahman Prapti, Alamgir Hasan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 5, 2024
Novel Insights into the Genetic Basis of Progressive Supranuclear Palsy in Asian-Indian Population
Saikat Dey, Monojit Debnath, Ramchandra Yelamanchi, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
January 12, 2024
Morphometric alterations of the mesocorticolimbic network in Parkinson's disease with impulse control disorders
Mohammed Farhan Ansari, Shweta Prasad, Sujas Bhardwaj, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 8, 2025
Movement Disorders after Dengue Virus Infection: A Scoping Review
Elena Cecilia Rosca, Divyani Garg, Santiago Perez-Lloret, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
June 23, 2025
Allelic Diversity, De Novo CAG Expansions and Intergenerational Instability at the HTT Locus in a Sample from India
Nikhil Ratna, Sowmya Devatha Venkatesh, Swathi Pasupulati, et al.
Journal of Genetics
|
April 19, 2018
Genetic testing for clinically suspected spinocerebellar ataxias: report from a tertiary referral centre in India
Sowmya 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.
Metabolites
|
July 26, 2024
Non-Alcoholic Fatty Liver Disease Induced by Feeding Medium-Chain Fatty Acids Upregulates Cholesterol and Lipid Homeostatic Genes in Skeletal Muscle of Neonatal Pigs
Samuel D Gerrard, Fernando H Biase, Joseph A Yonke, 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 syndrome
Riyanka Kumari, Vikram V Holla, Prashant Phulpagar, et al.
Page
of 43
Search research articles
Search
Showing results (341-350 of 430) with videos related to
Sort By:
Page
of 43
Annals of Indian Academy of Neurology
|
March 18, 2024
Association of Insulin-like Growth Factor-1 and Neurofilament Light Chain in Patients with Progressive Supranuclear Palsy
Saikat Dey, Ramachadra Yelamanchi, Thrinath Mullapudi, et al.
Plos One
|
September 12, 2025
Virulence gene profile and antimicrobial resistance patterns of Aeromonas hydrophila in farmed catfishes (Heteropneustes fossilis and Pangasianodon hypophthalmus) for the first time in Bangladesh
Farjana Ferdousi, Bushra Benta Rahman Prapti, Alamgir Hasan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 5, 2024
Novel Insights into the Genetic Basis of Progressive Supranuclear Palsy in Asian-Indian Population
Saikat Dey, Monojit Debnath, Ramchandra Yelamanchi, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
January 12, 2024
Morphometric alterations of the mesocorticolimbic network in Parkinson's disease with impulse control disorders
Mohammed Farhan Ansari, Shweta Prasad, Sujas Bhardwaj, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 8, 2025
Movement Disorders after Dengue Virus Infection: A Scoping Review
Elena Cecilia Rosca, Divyani Garg, Santiago Perez-Lloret, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
June 23, 2025
Allelic Diversity, De Novo CAG Expansions and Intergenerational Instability at the HTT Locus in a Sample from India
Nikhil Ratna, Sowmya Devatha Venkatesh, Swathi Pasupulati, et al.
Journal of Genetics
|
April 19, 2018
Genetic testing for clinically suspected spinocerebellar ataxias: report from a tertiary referral centre in India
Sowmya 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.
Metabolites
|
July 26, 2024
Non-Alcoholic Fatty Liver Disease Induced by Feeding Medium-Chain Fatty Acids Upregulates Cholesterol and Lipid Homeostatic Genes in Skeletal Muscle of Neonatal Pigs
Samuel D Gerrard, Fernando H Biase, Joseph A Yonke, 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 syndrome
Riyanka Kumari, Vikram V Holla, Prashant Phulpagar, et al.
Page
of 43