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Acta Neuropathologica
|
April 9, 2008
Changes in skeletal muscle expression of AQP1 and AQP4 in dystrophinopathy and dysferlinopathy patients
Carol G Au, Tanya L Butler, Jonathan R Egan, et al.
JAMA Network Open
|
December 6, 2021
Auditory Dysfunction Among Individuals With Neurofibromatosis Type 1
Gary Rance, Julien Zanin, Alice Maier, et al.
Neurology
|
February 1, 1996
Cognitive dysfunction as the major presenting feature of Becker's muscular dystrophy
K N North, G Miller, S T Iannaccone, et al.
Nature Communications
|
February 1, 2017
Evidence for ACTN3 as a genetic modifier of Duchenne muscular dystrophy
Marshall W Hogarth, Peter J Houweling, Kristen C Thomas, et al.
Annals of Neurology
|
September 18, 2001
Nemaline myopathy: a clinical study of 143 cases
M 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-actin
Carina 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 myopathy
K 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 gliomas
K 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 cells
Emily 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 Healthcare
Zornitza Stark, Tiffany Boughtwood, Peta Phillips, et al.
Page
of 34
Search research articles
Search
Showing results (201-210 of 333) with videos related to
Sort By:
Page
of 34
Acta Neuropathologica
|
April 9, 2008
Changes in skeletal muscle expression of AQP1 and AQP4 in dystrophinopathy and dysferlinopathy patients
Carol G Au, Tanya L Butler, Jonathan R Egan, et al.
JAMA Network Open
|
December 6, 2021
Auditory Dysfunction Among Individuals With Neurofibromatosis Type 1
Gary Rance, Julien Zanin, Alice Maier, et al.
Neurology
|
February 1, 1996
Cognitive dysfunction as the major presenting feature of Becker's muscular dystrophy
K N North, G Miller, S T Iannaccone, et al.
Nature Communications
|
February 1, 2017
Evidence for ACTN3 as a genetic modifier of Duchenne muscular dystrophy
Marshall W Hogarth, Peter J Houweling, Kristen C Thomas, et al.
Annals of Neurology
|
September 18, 2001
Nemaline myopathy: a clinical study of 143 cases
M 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-actin
Carina 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 myopathy
K 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 gliomas
K 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 cells
Emily 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 Healthcare
Zornitza Stark, Tiffany Boughtwood, Peta Phillips, et al.
Page
of 34