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O Crawford

Showing results (121-130 of 190) with videos related to

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Muscle & Nerve|January 27, 2021
Safety and efficacy of nusinersen in spinal muscular atrophy: The EMBRACE studyGyula Acsadi, Thomas O Crawford, Wolfgang Müller-Felber, et al.
Nature Genetics|January 1, 1995
A novel cDNA detects homozygous microdeletions in greater than 50% of type I spinal muscular atrophy patientsT G Thompson, C J DiDonato, L R Simard, et al.
The American Journal of Geriatric Psychiatry. Open Science, Education, and Practice|December 17, 2025
Older Adult Volunteers' Experiences Delivering a Lay-Led Behavioral Activation Program for Depression Among Community-Dwelling Older Adults: A Mixed Methods StudyNicole O Crawford, Lesley Steinman, Isabel Rollandi, et al.
Muscle & Nerve|October 6, 2017
Charcot-Marie-Tooth Disease type 4C: Novel mutations, clinical presentations, and diagnostic challengesNivedita U Jerath, Ami Mankodi, Thomas O Crawford, et al.
Journal of Child Neurology|September 1, 2007
Consensus statement for standard of care in spinal muscular atrophyChing H Wang, Richard S Finkel, Enrico S Bertini, et al.
Annals of Clinical and Translational Neurology|February 16, 2022
TRPV4 mutations causing mixed neuropathy and skeletal phenotypes result in severe gain of functionArens Taga, Margo A Peyton, Benedikt Goretzki, et al.
Journal of Child Neurology|April 1, 2014
High-dose glucocorticoid therapy in the management of seizures in neonatal incontinentia pigmenti: a case reportDavid S Wolf, W Christopher Golden, Julie Hoover-Fong, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 2, 2003
Human embryonic germ cell derivatives facilitate motor recovery of rats with diffuse motor neuron injuryDouglas A Kerr, Jerònia Lladó, Michael J Shamblott, et al.
Spine|July 7, 2011
Growing rods for scoliosis in spinal muscular atrophy: structural effects, complications, and hospital staysMark J McElroy, Adam C Shaner, Thomas O Crawford, et al.
Human Molecular Genetics|January 8, 2008
Neuronal SMN expression corrects spinal muscular atrophy in severe SMA mice while muscle-specific SMN expression has no phenotypic effectTatiana O Gavrilina, Vicki L McGovern, Eileen Workman, et al.
Pageof 19

Showing results (121-130 of 190) with videos related to

Sort By:
Pageof 19
Muscle & Nerve|January 27, 2021
Safety and efficacy of nusinersen in spinal muscular atrophy: The EMBRACE studyGyula Acsadi, Thomas O Crawford, Wolfgang Müller-Felber, et al.
Nature Genetics|January 1, 1995
A novel cDNA detects homozygous microdeletions in greater than 50% of type I spinal muscular atrophy patientsT G Thompson, C J DiDonato, L R Simard, et al.
The American Journal of Geriatric Psychiatry. Open Science, Education, and Practice|December 17, 2025
Older Adult Volunteers' Experiences Delivering a Lay-Led Behavioral Activation Program for Depression Among Community-Dwelling Older Adults: A Mixed Methods StudyNicole O Crawford, Lesley Steinman, Isabel Rollandi, et al.
Muscle & Nerve|October 6, 2017
Charcot-Marie-Tooth Disease type 4C: Novel mutations, clinical presentations, and diagnostic challengesNivedita U Jerath, Ami Mankodi, Thomas O Crawford, et al.
Journal of Child Neurology|September 1, 2007
Consensus statement for standard of care in spinal muscular atrophyChing H Wang, Richard S Finkel, Enrico S Bertini, et al.
Annals of Clinical and Translational Neurology|February 16, 2022
TRPV4 mutations causing mixed neuropathy and skeletal phenotypes result in severe gain of functionArens Taga, Margo A Peyton, Benedikt Goretzki, et al.
Journal of Child Neurology|April 1, 2014
High-dose glucocorticoid therapy in the management of seizures in neonatal incontinentia pigmenti: a case reportDavid S Wolf, W Christopher Golden, Julie Hoover-Fong, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 2, 2003
Human embryonic germ cell derivatives facilitate motor recovery of rats with diffuse motor neuron injuryDouglas A Kerr, Jerònia Lladó, Michael J Shamblott, et al.
Spine|July 7, 2011
Growing rods for scoliosis in spinal muscular atrophy: structural effects, complications, and hospital staysMark J McElroy, Adam C Shaner, Thomas O Crawford, et al.
Human Molecular Genetics|January 8, 2008
Neuronal SMN expression corrects spinal muscular atrophy in severe SMA mice while muscle-specific SMN expression has no phenotypic effectTatiana O Gavrilina, Vicki L McGovern, Eileen Workman, et al.
Pageof 19