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Natalie Keller

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

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Health & Justice|February 19, 2026
Healthcare in a system of punishment: how clinicians experience care work within carceral settingsNatalie Keller, Andrew Sudler, Leslie Riddle, et al.
European Journal of Medical Genetics|January 2, 2021
De novo DNM1L variant presenting with severe muscular atrophy, dystonia and sensory neuropathyNatalie Keller, Cem Paketci, Pinar Edem, et al.
Movement Disorders Clinical Practice|July 26, 2021
VPS13D: One Family, Same Mutations, Two PhenotypesJan Niklas Petry-Schmelzer, Natalie Keller, Mert Karakaya, et al.
Neuromuscular Disorders : NMD|June 12, 2020
Hereditary polyneuropathy with optic atrophy due to PDXK variant leading to impaired Vitamin B6 metabolismNatalie Keller, Natalia Mendoza-Ferreira, Reza Maroofian, et al.
Human Mutation|February 18, 2021
Genomic variants causing mitochondrial dysfunction are common in hereditary lower motor neuron diseaseNatalie Keller, Cem Paketci, Janine Altmueller, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|April 15, 2026
Behavioral Incentives for Exercise and Intra-Articular Corticosteroids for Knee Osteoarthritis: Results from a Factorially Designed Pragmatic Randomized Clinical TrialJoshua F Baker, Katherine D Wysham, Mercedes Quinones, et al.
Pageof 1

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

Sort By:
Pageof 1
Health & Justice|February 19, 2026
Healthcare in a system of punishment: how clinicians experience care work within carceral settingsNatalie Keller, Andrew Sudler, Leslie Riddle, et al.
European Journal of Medical Genetics|January 2, 2021
De novo DNM1L variant presenting with severe muscular atrophy, dystonia and sensory neuropathyNatalie Keller, Cem Paketci, Pinar Edem, et al.
Movement Disorders Clinical Practice|July 26, 2021
VPS13D: One Family, Same Mutations, Two PhenotypesJan Niklas Petry-Schmelzer, Natalie Keller, Mert Karakaya, et al.
Neuromuscular Disorders : NMD|June 12, 2020
Hereditary polyneuropathy with optic atrophy due to PDXK variant leading to impaired Vitamin B6 metabolismNatalie Keller, Natalia Mendoza-Ferreira, Reza Maroofian, et al.
Human Mutation|February 18, 2021
Genomic variants causing mitochondrial dysfunction are common in hereditary lower motor neuron diseaseNatalie Keller, Cem Paketci, Janine Altmueller, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|April 15, 2026
Behavioral Incentives for Exercise and Intra-Articular Corticosteroids for Knee Osteoarthritis: Results from a Factorially Designed Pragmatic Randomized Clinical TrialJoshua F Baker, Katherine D Wysham, Mercedes Quinones, et al.
Pageof 1