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N North

Showing results (201-210 of 333) with videos related to

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Acta Neuropathologica|April 9, 2008
Changes in skeletal muscle expression of AQP1 and AQP4 in dystrophinopathy and dysferlinopathy patientsCarol G Au, Tanya L Butler, Jonathan R Egan, et al.
JAMA Network Open|December 6, 2021
Auditory Dysfunction Among Individuals With Neurofibromatosis Type 1Gary Rance, Julien Zanin, Alice Maier, et al.
Neurology|February 1, 1996
Cognitive dysfunction as the major presenting feature of Becker's muscular dystrophyK N North, G Miller, S T Iannaccone, et al.
Nature Communications|February 1, 2017
Evidence for ACTN3 as a genetic modifier of Duchenne muscular dystrophyMarshall W Hogarth, Peter J Houweling, Kristen C Thomas, et al.
Annals of Neurology|September 18, 2001
Nemaline myopathy: a clinical study of 143 casesM M Ryan, C Schnell, C D Strickland, et al.
Neuromuscular Disorders : NMD|September 1, 2004
Genotype-phenotype correlations in nemaline myopathy caused by mutations in the genes for nebulin and skeletal muscle alpha-actinCarina Wallgren-Pettersson, Katarina Pelin, Kristen J Nowak, et al.
Neuromuscular Disorders : NMD|August 6, 2003
Deficiency of the syntrophins and alpha-dystrobrevin in patients with inherited myopathyK J Jones, A G Compton, N Yang, et al.
Familial Cancer|July 26, 2012
Parent-of-origin in individuals with familial neurofibromatosis type 1 and optic pathway gliomasK J Johnson, M J Fisher, R L Listernick, et al.
Brain : a Journal of Neurology|May 26, 2012
Autosomal dominant congenital spinal muscular atrophy: a true form of spinal muscular atrophy caused by early loss of anterior horn cellsEmily C Oates, Stephen Reddel, Michael L Rodriguez, et al.
American Journal of Human Genetics|July 5, 2019
Australian Genomics: A Federated Model for Integrating Genomics into HealthcareZornitza Stark, Tiffany Boughtwood, Peta Phillips, et al.
Pageof 34

Showing results (201-210 of 333) with videos related to

Sort By:
Pageof 34
Acta Neuropathologica|April 9, 2008
Changes in skeletal muscle expression of AQP1 and AQP4 in dystrophinopathy and dysferlinopathy patientsCarol G Au, Tanya L Butler, Jonathan R Egan, et al.
JAMA Network Open|December 6, 2021
Auditory Dysfunction Among Individuals With Neurofibromatosis Type 1Gary Rance, Julien Zanin, Alice Maier, et al.
Neurology|February 1, 1996
Cognitive dysfunction as the major presenting feature of Becker's muscular dystrophyK N North, G Miller, S T Iannaccone, et al.
Nature Communications|February 1, 2017
Evidence for ACTN3 as a genetic modifier of Duchenne muscular dystrophyMarshall W Hogarth, Peter J Houweling, Kristen C Thomas, et al.
Annals of Neurology|September 18, 2001
Nemaline myopathy: a clinical study of 143 casesM M Ryan, C Schnell, C D Strickland, et al.
Neuromuscular Disorders : NMD|September 1, 2004
Genotype-phenotype correlations in nemaline myopathy caused by mutations in the genes for nebulin and skeletal muscle alpha-actinCarina Wallgren-Pettersson, Katarina Pelin, Kristen J Nowak, et al.
Neuromuscular Disorders : NMD|August 6, 2003
Deficiency of the syntrophins and alpha-dystrobrevin in patients with inherited myopathyK J Jones, A G Compton, N Yang, et al.
Familial Cancer|July 26, 2012
Parent-of-origin in individuals with familial neurofibromatosis type 1 and optic pathway gliomasK J Johnson, M J Fisher, R L Listernick, et al.
Brain : a Journal of Neurology|May 26, 2012
Autosomal dominant congenital spinal muscular atrophy: a true form of spinal muscular atrophy caused by early loss of anterior horn cellsEmily C Oates, Stephen Reddel, Michael L Rodriguez, et al.
American Journal of Human Genetics|July 5, 2019
Australian Genomics: A Federated Model for Integrating Genomics into HealthcareZornitza Stark, Tiffany Boughtwood, Peta Phillips, et al.
Pageof 34