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Sangeetha Yoganathan

Showing results (71-80 of 89) with videos related to

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Neurology India|November 15, 2016
Biotin thiamine responsive basal ganglia disease-A potentially treatable inborn error of metabolismKarthik Muthusamy, Alka V Ekbote, Maya M Thomas, et al.
European Journal of Medical Genetics|April 19, 2023
Exploration of clinical and genetic findings in Ataxia-Telangiectasia (AT) patients from the Indian subcontinentSweta Das, Maya Thomas, Sangeetha Yoganathan, et al.
Movement Disorders Clinical Practice|July 4, 2025
Deep Brain Stimulation in a Child with Aicardi-Goutières Syndrome-7 (AGS7): A Case Report and Literature ReviewSangeetha Yoganathan, Siddharth Seth, Sunita Venkateswaran, et al.
American Journal of Medical Genetics. Part A|May 3, 2025
A Novel Presentation and Variable Phenotypic Spectrum of Homozygous Start-Loss Variant in LYRM7-Associated Mitochondrial Complex III DeficiencyNoel Deep Luke, Aditya Vijayakrishnan Nair, Ajith Sivadasan, et al.
Pediatric Neurology|July 6, 2023
Childhood Neurological Disorders With Hyperhomocystinemia: A Case-Based ReviewSangeetha Yoganathan, Himani Bhasin, Divyani Garg, et al.
Movement Disorders Clinical Practice|April 6, 2026
Phenotypic Clues in Infantile-Onset Parkinsonism-Dystonia-2: A Treatable Neurotransmitter DisorderSangeetha Yoganathan, Haya S AlFaris, Lindsey Vogt, et al.
European Journal of Medical Genetics|July 25, 2021
Phenotypic variability of a TREX1 variant in Aicardi-Goutieres type 1 patients from the Indian subcontinentSuneetha Susan Cleave Abraham, Sangeetha Yoganathan, Beena Koshy, et al.
Neurochemistry International|December 30, 2019
Phosphoproteomic analysis reveals Akt isoform-specific regulation of cytoskeleton proteins in human temporal lobe epilepsy with hippocampal sclerosisRajesh Ramanna Valmiki, Subhashini Venkatesalu, Ari George Chacko, et al.
Movement Disorders Clinical Practice|May 11, 2026
GLUT1 Deficiency Syndrome with Coexistent Movement Disorder and AnemiaSangeetha Yoganathan, Haya S AlFaris, Anika Menetrey, et al.
Movement Disorders Clinical Practice|September 1, 2025
Early Onset Dystonia, Parkinsonism, and Spasticity in Siblings with VAC14-Associated Neurodegeneration: A Case Report and Literature ReviewRebecca Lindsay, Sangeetha Yoganathan, Wei Kang Lim, et al.
Pageof 9

Showing results (71-80 of 89) with videos related to

Sort By:
Pageof 9
Neurology India|November 15, 2016
Biotin thiamine responsive basal ganglia disease-A potentially treatable inborn error of metabolismKarthik Muthusamy, Alka V Ekbote, Maya M Thomas, et al.
European Journal of Medical Genetics|April 19, 2023
Exploration of clinical and genetic findings in Ataxia-Telangiectasia (AT) patients from the Indian subcontinentSweta Das, Maya Thomas, Sangeetha Yoganathan, et al.
Movement Disorders Clinical Practice|July 4, 2025
Deep Brain Stimulation in a Child with Aicardi-Goutières Syndrome-7 (AGS7): A Case Report and Literature ReviewSangeetha Yoganathan, Siddharth Seth, Sunita Venkateswaran, et al.
American Journal of Medical Genetics. Part A|May 3, 2025
A Novel Presentation and Variable Phenotypic Spectrum of Homozygous Start-Loss Variant in LYRM7-Associated Mitochondrial Complex III DeficiencyNoel Deep Luke, Aditya Vijayakrishnan Nair, Ajith Sivadasan, et al.
Pediatric Neurology|July 6, 2023
Childhood Neurological Disorders With Hyperhomocystinemia: A Case-Based ReviewSangeetha Yoganathan, Himani Bhasin, Divyani Garg, et al.
Movement Disorders Clinical Practice|April 6, 2026
Phenotypic Clues in Infantile-Onset Parkinsonism-Dystonia-2: A Treatable Neurotransmitter DisorderSangeetha Yoganathan, Haya S AlFaris, Lindsey Vogt, et al.
European Journal of Medical Genetics|July 25, 2021
Phenotypic variability of a TREX1 variant in Aicardi-Goutieres type 1 patients from the Indian subcontinentSuneetha Susan Cleave Abraham, Sangeetha Yoganathan, Beena Koshy, et al.
Neurochemistry International|December 30, 2019
Phosphoproteomic analysis reveals Akt isoform-specific regulation of cytoskeleton proteins in human temporal lobe epilepsy with hippocampal sclerosisRajesh Ramanna Valmiki, Subhashini Venkatesalu, Ari George Chacko, et al.
Movement Disorders Clinical Practice|May 11, 2026
GLUT1 Deficiency Syndrome with Coexistent Movement Disorder and AnemiaSangeetha Yoganathan, Haya S AlFaris, Anika Menetrey, et al.
Movement Disorders Clinical Practice|September 1, 2025
Early Onset Dystonia, Parkinsonism, and Spasticity in Siblings with VAC14-Associated Neurodegeneration: A Case Report and Literature ReviewRebecca Lindsay, Sangeetha Yoganathan, Wei Kang Lim, et al.
Pageof 9