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David N Herrmann

Showing results (101-110 of 128) with videos related to

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JAMA Neurology|April 5, 2016
Phenotypic Variability of Childhood Charcot-Marie-Tooth DiseaseKayla M D Cornett, Manoj P Menezes, Paula Bray, et al.
Journal of the Peripheral Nervous System : JPNS|April 6, 2024
A study concept of expeditious clinical enrollment for genetic modifier studies in Charcot-Marie-Tooth neuropathy 1AIsaac R L Xu, Matt C Danzi, Ariel Ruiz, et al.
Neurology|May 11, 2022
Randomized Phase 2 Study of ACE-083 in Patients With Charcot-Marie-Tooth DiseaseFlorian P Thomas, Thomas H Brannagan, Russell J Butterfield, et al.
Brain : a Journal of Neurology|August 28, 2015
Genotype-phenotype characteristics and baseline natural history of heritable neuropathies caused by mutations in the MPZ geneOranee Sanmaneechai, Shawna Feely, Steven S Scherer, et al.
Brain : a Journal of Neurology|January 17, 2019
Erratum to: Development and validation of the Charcot-Marie-Tooth Disease Infant ScaleMelissa R Mandarakas, Manoj P Menezes, Kristy J Rose, et al.
Brain : a Journal of Neurology|November 27, 2018
Development and validation of the Charcot-Marie-Tooth Disease Infant ScaleMelissa R Mandarakas, Manoj P Menezes, Kristy J Rose, et al.
Neurology|October 15, 2020
Idiopathic distal sensory polyneuropathy: ACTTION diagnostic criteriaRoy Freeman, Jennifer S Gewandter, Catharina G Faber, et al.
Journal of Clinical Neuromuscular Disease|December 17, 2008
Diagnosis and Treatment of Chronic Immune-mediated NeuropathiesNorman Latov, Kenneth C Gorson, Thomas H Brannagan, et al.
Neurology|September 8, 2021
Association Between Body Mass Index and Disability in Children With Charcot-Marie-Tooth DiseaseGabrielle A Donlevy, Sarah P Garnett, Kayla M D Cornett, et al.
American Journal of Human Genetics|May 14, 2013
Mutations in BICD2 cause dominant congenital spinal muscular atrophy and hereditary spastic paraplegiaEmily C Oates, Alexander M Rossor, Majid Hafezparast, et al.
Pageof 13

Showing results (101-110 of 128) with videos related to

Sort By:
Pageof 13
JAMA Neurology|April 5, 2016
Phenotypic Variability of Childhood Charcot-Marie-Tooth DiseaseKayla M D Cornett, Manoj P Menezes, Paula Bray, et al.
Journal of the Peripheral Nervous System : JPNS|April 6, 2024
A study concept of expeditious clinical enrollment for genetic modifier studies in Charcot-Marie-Tooth neuropathy 1AIsaac R L Xu, Matt C Danzi, Ariel Ruiz, et al.
Neurology|May 11, 2022
Randomized Phase 2 Study of ACE-083 in Patients With Charcot-Marie-Tooth DiseaseFlorian P Thomas, Thomas H Brannagan, Russell J Butterfield, et al.
Brain : a Journal of Neurology|August 28, 2015
Genotype-phenotype characteristics and baseline natural history of heritable neuropathies caused by mutations in the MPZ geneOranee Sanmaneechai, Shawna Feely, Steven S Scherer, et al.
Brain : a Journal of Neurology|January 17, 2019
Erratum to: Development and validation of the Charcot-Marie-Tooth Disease Infant ScaleMelissa R Mandarakas, Manoj P Menezes, Kristy J Rose, et al.
Brain : a Journal of Neurology|November 27, 2018
Development and validation of the Charcot-Marie-Tooth Disease Infant ScaleMelissa R Mandarakas, Manoj P Menezes, Kristy J Rose, et al.
Neurology|October 15, 2020
Idiopathic distal sensory polyneuropathy: ACTTION diagnostic criteriaRoy Freeman, Jennifer S Gewandter, Catharina G Faber, et al.
Journal of Clinical Neuromuscular Disease|December 17, 2008
Diagnosis and Treatment of Chronic Immune-mediated NeuropathiesNorman Latov, Kenneth C Gorson, Thomas H Brannagan, et al.
Neurology|September 8, 2021
Association Between Body Mass Index and Disability in Children With Charcot-Marie-Tooth DiseaseGabrielle A Donlevy, Sarah P Garnett, Kayla M D Cornett, et al.
American Journal of Human Genetics|May 14, 2013
Mutations in BICD2 cause dominant congenital spinal muscular atrophy and hereditary spastic paraplegiaEmily C Oates, Alexander M Rossor, Majid Hafezparast, et al.
Pageof 13