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Showing results (401-410 of 415) with videos related to

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Parkinsonism & Related Disorders|November 16, 2019
Whole genome sequencing for the genetic diagnosis of heterogenous dystonia phenotypesKishore R Kumar, Ryan L Davis, Michel C Tchan, et al.
Disease Models & Mechanisms|August 12, 2010
Disease-specific, neurosphere-derived cells as models for brain disordersNicholas Matigian, Greger Abrahamsen, Ratneswary Sutharsan, et al.
Lancet (London, England)|December 24, 2016
Home use of a bihormonal bionic pancreas versus insulin pump therapy in adults with type 1 diabetes: a multicentre randomised crossover trialFiras H El-Khatib, Courtney Balliro, Mallory A Hillard, et al.
Brain : a Journal of Neurology|August 13, 2015
Allogeneic haematopoietic stem cell transplantation for mitochondrial neurogastrointestinal encephalomyopathyJoerg P Halter, W Michael, M Schüpbach, et al.
ALTEX|October 12, 2013
Lessons learned, challenges, and opportunities: the U.S. Endocrine Disruptor Screening ProgramDaland R Juberg, Susan J Borghoff, Richard A Becker, et al.
Parkinsonism & Related Disorders|May 21, 2024
Genome sequencing reanalysis increases the diagnostic yield in dystoniaAvi Fellner, Gurusidheshwar M Wali, Neil Mahant, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 28, 2017
Patient care standards for primary mitochondrial disease: a consensus statement from the Mitochondrial Medicine SocietySumit Parikh, Amy Goldstein, Amel Karaa, et al.
Nature Communications|July 4, 2026
Targeted long-read sequencing enables comprehensive analysis of the genetic and epigenetic landscape of inherited myopathiesDennis Yeow, Andre L M Reis, Igor Stevanovski, et al.
ALTEX|April 16, 2025
Developmental neurotoxicity (DNT): A call for implementation of new approach methodologies for regulatory purposes: Summary of the 5th International Conference on DNT TestingIvana Celardo, Michael Aschner, Randolph S Ashton, et al.
Annals of Neurology|August 19, 2020
Loss-of-Function Variants in HOPS Complex Genes VPS16 and VPS41 Cause Early Onset Dystonia Associated with Lysosomal AbnormalitiesDora Steel, Michael Zech, Chen Zhao, et al.
Pageof 42

Showing results (401-410 of 415) with videos related to

Sort By:
Pageof 42
Parkinsonism & Related Disorders|November 16, 2019
Whole genome sequencing for the genetic diagnosis of heterogenous dystonia phenotypesKishore R Kumar, Ryan L Davis, Michel C Tchan, et al.
Disease Models & Mechanisms|August 12, 2010
Disease-specific, neurosphere-derived cells as models for brain disordersNicholas Matigian, Greger Abrahamsen, Ratneswary Sutharsan, et al.
Lancet (London, England)|December 24, 2016
Home use of a bihormonal bionic pancreas versus insulin pump therapy in adults with type 1 diabetes: a multicentre randomised crossover trialFiras H El-Khatib, Courtney Balliro, Mallory A Hillard, et al.
Brain : a Journal of Neurology|August 13, 2015
Allogeneic haematopoietic stem cell transplantation for mitochondrial neurogastrointestinal encephalomyopathyJoerg P Halter, W Michael, M Schüpbach, et al.
ALTEX|October 12, 2013
Lessons learned, challenges, and opportunities: the U.S. Endocrine Disruptor Screening ProgramDaland R Juberg, Susan J Borghoff, Richard A Becker, et al.
Parkinsonism & Related Disorders|May 21, 2024
Genome sequencing reanalysis increases the diagnostic yield in dystoniaAvi Fellner, Gurusidheshwar M Wali, Neil Mahant, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 28, 2017
Patient care standards for primary mitochondrial disease: a consensus statement from the Mitochondrial Medicine SocietySumit Parikh, Amy Goldstein, Amel Karaa, et al.
Nature Communications|July 4, 2026
Targeted long-read sequencing enables comprehensive analysis of the genetic and epigenetic landscape of inherited myopathiesDennis Yeow, Andre L M Reis, Igor Stevanovski, et al.
ALTEX|April 16, 2025
Developmental neurotoxicity (DNT): A call for implementation of new approach methodologies for regulatory purposes: Summary of the 5th International Conference on DNT TestingIvana Celardo, Michael Aschner, Randolph S Ashton, et al.
Annals of Neurology|August 19, 2020
Loss-of-Function Variants in HOPS Complex Genes VPS16 and VPS41 Cause Early Onset Dystonia Associated with Lysosomal AbnormalitiesDora Steel, Michael Zech, Chen Zhao, et al.
Pageof 42