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Showing results (171-180 of 190) with videos related to

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Neuromuscular Disorders : NMD|January 2, 2018
Diagnosis and management of spinal muscular atrophy: Part 1: Recommendations for diagnosis, rehabilitation, orthopedic and nutritional careEugenio Mercuri, Richard S Finkel, Francesco Muntoni, et al.
Nature|April 21, 2022
Multi-qubit entanglement and algorithms on a neutral-atom quantum computerT M Graham, Y Song, J Scott, et al.
Neuromuscular Disorders : NMD|January 7, 2018
Diagnosis and management of spinal muscular atrophy: Part 2: Pulmonary and acute care; medications, supplements and immunizations; other organ systems; and ethicsRichard S Finkel, Eugenio Mercuri, Oscar H Meyer, et al.
The Journal of Clinical Investigation|October 8, 2019
Age-dependent SMN expression in disease-relevant tissue and implications for SMA treatmentDaniel M Ramos, Constantin d'Ydewalle, Vijayalakshmi Gabbeta, et al.
Brain : a Journal of Neurology|July 18, 2024
Combined clinical, structural and cellular studies discriminate pathogenic and benign TRPV4 variantsSarah H Berth, Linh Vo, Do Hoon Kwon, et al.
Human Mutation|September 11, 2014
Mosaicism for dominant collagen 6 mutations as a cause for intrafamilial phenotypic variabilitySandra Donkervoort, Ying Hu, Tanya Stojkovic, et al.
Plos One|April 9, 2013
SMA-MAP: a plasma protein panel for spinal muscular atrophyDione T Kobayashi, Jing Shi, Laurie Stephen, et al.
Muscle & Nerve|August 24, 2017
Clinical trial of L-Carnitine and valproic acid in spinal muscular atrophy type IKristin J Krosschell, John T Kissel, Elise L Townsend, et al.
Science Translational Medicine|January 28, 2021
Impaired prenatal motor axon development necessitates early therapeutic intervention in severe SMALingling Kong, David O Valdivia, Christian M Simon, et al.
Human Mutation|February 15, 2022
Intron mutations and early transcription termination in Duchenne and Becker muscular dystrophyMegan A Waldrop, Steven A Moore, Katherine D Mathews, et al.
Pageof 19

Showing results (171-180 of 190) with videos related to

Sort By:
Pageof 19
Neuromuscular Disorders : NMD|January 2, 2018
Diagnosis and management of spinal muscular atrophy: Part 1: Recommendations for diagnosis, rehabilitation, orthopedic and nutritional careEugenio Mercuri, Richard S Finkel, Francesco Muntoni, et al.
Nature|April 21, 2022
Multi-qubit entanglement and algorithms on a neutral-atom quantum computerT M Graham, Y Song, J Scott, et al.
Neuromuscular Disorders : NMD|January 7, 2018
Diagnosis and management of spinal muscular atrophy: Part 2: Pulmonary and acute care; medications, supplements and immunizations; other organ systems; and ethicsRichard S Finkel, Eugenio Mercuri, Oscar H Meyer, et al.
The Journal of Clinical Investigation|October 8, 2019
Age-dependent SMN expression in disease-relevant tissue and implications for SMA treatmentDaniel M Ramos, Constantin d'Ydewalle, Vijayalakshmi Gabbeta, et al.
Brain : a Journal of Neurology|July 18, 2024
Combined clinical, structural and cellular studies discriminate pathogenic and benign TRPV4 variantsSarah H Berth, Linh Vo, Do Hoon Kwon, et al.
Human Mutation|September 11, 2014
Mosaicism for dominant collagen 6 mutations as a cause for intrafamilial phenotypic variabilitySandra Donkervoort, Ying Hu, Tanya Stojkovic, et al.
Plos One|April 9, 2013
SMA-MAP: a plasma protein panel for spinal muscular atrophyDione T Kobayashi, Jing Shi, Laurie Stephen, et al.
Muscle & Nerve|August 24, 2017
Clinical trial of L-Carnitine and valproic acid in spinal muscular atrophy type IKristin J Krosschell, John T Kissel, Elise L Townsend, et al.
Science Translational Medicine|January 28, 2021
Impaired prenatal motor axon development necessitates early therapeutic intervention in severe SMALingling Kong, David O Valdivia, Christian M Simon, et al.
Human Mutation|February 15, 2022
Intron mutations and early transcription termination in Duchenne and Becker muscular dystrophyMegan A Waldrop, Steven A Moore, Katherine D Mathews, et al.
Pageof 19