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Sumit Parikh

Showing results (11-20 of 97) with videos related to

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Handbook of Clinical Neurology|February 22, 2023
Currently available therapies in mitochondrial diseaseCornelia Kornblum, Costanza Lamperti, Sumit Parikh
British Journal of Haematology|April 4, 2019
Complication rates of central venous access devices in patients with inherited bleeding disorders in AustraliaSally Campbell, Sumit Parikh, Huyen A Tran
Pediatric Neurology|May 13, 2009
Vitamins, not surgery: spinal fluid testing in hemispheric epilepsySumit Parikh, Keith Hyland, Deepak K Lachhwani
Molecular Genetics and Metabolism|December 4, 2021
Pediatric single large-scale mtDNA deletion syndromes: The power of patient reported outcomesElizabeth Reynolds, Matthew Byrne, Rebecca Ganetzky, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 4, 2020
The Australian experience with switching to extended half-life factor VIII and IX concentrates: On behalf of the Australian Haemophilia Centre Directors' OrganisationYvonne Brennan, Sumit Parikh, Simon McRae, et al.
Ophthalmic Genetics|April 1, 2016
Ophthalmological findings in 74 patients with mitochondrial diseaseCheng-Cheng Zhu, Elias I Traboulsi, Sumit Parikh
Ophthalmic Genetics|July 22, 2016
Authors' response to Finsterer and Zarrouk-Mahjoub's commentsSumit Parikh, Cheng-Cheng Zhu, Elias I Traboulsi
Survey of Ophthalmology|February 21, 2021
Mitochondrial DNA A3243G variant-associated retinopathy: Current perspectives and clinical implicationsRazek Georges Coussa, Sumit Parikh, Elias I Traboulsi
European Heart Journal. Case Reports|August 12, 2024
Case report: severe hypertrophic cardiomyopathy in a female neonate caused by <i>de novo</i> variant in <i>NDUFB11</i>Javeria Tariq, Madeleine Townsend, Sumit Parikh, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|June 9, 2023
Epilepsy with eyelid myoclonia in the setting of de novo pathogenic variant in ATP1A3Maksim Parfyonov, Alina Ivaniuk, Sumit Parikh, et al.
Pageof 10

Showing results (11-20 of 97) with videos related to

Sort By:
Pageof 10
Handbook of Clinical Neurology|February 22, 2023
Currently available therapies in mitochondrial diseaseCornelia Kornblum, Costanza Lamperti, Sumit Parikh
British Journal of Haematology|April 4, 2019
Complication rates of central venous access devices in patients with inherited bleeding disorders in AustraliaSally Campbell, Sumit Parikh, Huyen A Tran
Pediatric Neurology|May 13, 2009
Vitamins, not surgery: spinal fluid testing in hemispheric epilepsySumit Parikh, Keith Hyland, Deepak K Lachhwani
Molecular Genetics and Metabolism|December 4, 2021
Pediatric single large-scale mtDNA deletion syndromes: The power of patient reported outcomesElizabeth Reynolds, Matthew Byrne, Rebecca Ganetzky, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 4, 2020
The Australian experience with switching to extended half-life factor VIII and IX concentrates: On behalf of the Australian Haemophilia Centre Directors' OrganisationYvonne Brennan, Sumit Parikh, Simon McRae, et al.
Ophthalmic Genetics|April 1, 2016
Ophthalmological findings in 74 patients with mitochondrial diseaseCheng-Cheng Zhu, Elias I Traboulsi, Sumit Parikh
Ophthalmic Genetics|July 22, 2016
Authors' response to Finsterer and Zarrouk-Mahjoub's commentsSumit Parikh, Cheng-Cheng Zhu, Elias I Traboulsi
Survey of Ophthalmology|February 21, 2021
Mitochondrial DNA A3243G variant-associated retinopathy: Current perspectives and clinical implicationsRazek Georges Coussa, Sumit Parikh, Elias I Traboulsi
European Heart Journal. Case Reports|August 12, 2024
Case report: severe hypertrophic cardiomyopathy in a female neonate caused by <i>de novo</i> variant in <i>NDUFB11</i>Javeria Tariq, Madeleine Townsend, Sumit Parikh, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|June 9, 2023
Epilepsy with eyelid myoclonia in the setting of de novo pathogenic variant in ATP1A3Maksim Parfyonov, Alina Ivaniuk, Sumit Parikh, et al.
Pageof 10