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Sharika Raga

Showing results (1-10 of 6) with videos related to

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Epileptic Disorders : International Epilepsy Journal with Videotape|June 9, 2021
Electroclinical markers to differentiate between focal and generalized epilepsiesSharika Raga, Sylvain Rheims, Nicola Specchio, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|February 26, 2021
Developmental and epileptic encephalopathies: recognition and approaches to careSharika Raga, Nicola Specchio, Sylvain Rheims, et al.
The Cochrane Database of Systematic Reviews|December 10, 2024
Treatments for RYR1-related disordersSharika Raga, Nicol Voermans, Ivan Perez-Neri, et al.
Molecular Genetics and Metabolism Reports|April 4, 2024
A novel mitochondrial DNA variant in <i>MT-ND6:</i> m.14430A>C p.(Trp82Gly) identified in a patient with Leigh syndrome and complex I deficiencySurita Meldau, Sally Ackermann, Gillian Riordan, et al.
Frontiers in Neurology|September 15, 2023
The mutational profile in a South African cohort with inherited neuropathies and spastic paraplegiaAmokelani C Mahungu, Elizabeth Steyn, Niki Floudiotis, et al.
Brain : a Journal of Neurology|July 30, 2023
Neuromuscular disease genetics in under-represented populations: increasing data diversityLindsay A Wilson, William L Macken, Luke D Perry, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Epileptic Disorders : International Epilepsy Journal with Videotape|June 9, 2021
Electroclinical markers to differentiate between focal and generalized epilepsiesSharika Raga, Sylvain Rheims, Nicola Specchio, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|February 26, 2021
Developmental and epileptic encephalopathies: recognition and approaches to careSharika Raga, Nicola Specchio, Sylvain Rheims, et al.
The Cochrane Database of Systematic Reviews|December 10, 2024
Treatments for RYR1-related disordersSharika Raga, Nicol Voermans, Ivan Perez-Neri, et al.
Molecular Genetics and Metabolism Reports|April 4, 2024
A novel mitochondrial DNA variant in <i>MT-ND6:</i> m.14430A>C p.(Trp82Gly) identified in a patient with Leigh syndrome and complex I deficiencySurita Meldau, Sally Ackermann, Gillian Riordan, et al.
Frontiers in Neurology|September 15, 2023
The mutational profile in a South African cohort with inherited neuropathies and spastic paraplegiaAmokelani C Mahungu, Elizabeth Steyn, Niki Floudiotis, et al.
Brain : a Journal of Neurology|July 30, 2023
Neuromuscular disease genetics in under-represented populations: increasing data diversityLindsay A Wilson, William L Macken, Luke D Perry, et al.
Pageof 1