Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Louis Viollet

Showing results (1-10 of 23) with videos related to

Pageof 3
Sort By:
Handbook of Clinical Neurology|April 30, 2013
Spinal muscular atrophiesLouis Viollet, Judith Melki
Journal of Child Neurology|July 31, 2003
Evoked potentials in spinal muscular atrophyFawzia Cheliout-Heraut, Annie Barois, Andoni Urtizberea, et al.
Journal of Cell Science|February 2, 2006
Distinct domains of the spinal muscular atrophy protein SMN are required for targeting to Cajal bodies in mammalian cellsBenoît Renvoisé, Kevinee Khoobarry, Marie-Claude Gendron, et al.
Human Molecular Genetics|January 9, 2009
The loss of the snoRNP chaperone Nopp140 from Cajal bodies of patient fibroblasts correlates with the severity of spinal muscular atrophyBenoît Renvoisé, Sabrina Colasse, Philippe Burlet, et al.
Human Molecular Genetics|April 30, 2002
A novel association of the SMN protein with two major non-ribosomal nucleolar proteins and its implication in spinal muscular atrophySuzie Lefebvre, Philippe Burlet, Louis Viollet, et al.
Scientific Reports|October 22, 2020
Reconstructing the hydraulics of the world's first industrial complex, the second century CE Barbegal watermills, FranceCees W Passchier, Marcel Bourgeois, Pierre-Louis Viollet, et al.
Brain : a Journal of Neurology|August 26, 2003
Dominant and recessive central core disease associated with RYR1 mutations and fetal akinesiaNorma Beatriz Romero, Nicole Monnier, Louis Viollet, et al.
British Journal of Clinical Pharmacology|February 3, 2011
Riluzole pharmacokinetics in young patients with spinal muscular atrophyChadi Abbara, Brigitte Estournet, Lucette Lacomblez, et al.
Journal of Neuromuscular Diseases|November 19, 2016
Orthopedic Management of Scoliosis by Garches Brace and Spinal Fusion in SMA Type 2 ChildrenMichela Catteruccia, Carole Vuillerot, Isabelle Vaugier, et al.
American Journal of Human Genetics|June 15, 2007
The nuclear factor kappaB-activator gene PLEKHG5 is mutated in a form of autosomal recessive lower motor neuron disease with childhood onsetIsabelle Maystadt, René Rezsöhazy, Martine Barkats, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Handbook of Clinical Neurology|April 30, 2013
Spinal muscular atrophiesLouis Viollet, Judith Melki
Journal of Child Neurology|July 31, 2003
Evoked potentials in spinal muscular atrophyFawzia Cheliout-Heraut, Annie Barois, Andoni Urtizberea, et al.
Journal of Cell Science|February 2, 2006
Distinct domains of the spinal muscular atrophy protein SMN are required for targeting to Cajal bodies in mammalian cellsBenoît Renvoisé, Kevinee Khoobarry, Marie-Claude Gendron, et al.
Human Molecular Genetics|January 9, 2009
The loss of the snoRNP chaperone Nopp140 from Cajal bodies of patient fibroblasts correlates with the severity of spinal muscular atrophyBenoît Renvoisé, Sabrina Colasse, Philippe Burlet, et al.
Human Molecular Genetics|April 30, 2002
A novel association of the SMN protein with two major non-ribosomal nucleolar proteins and its implication in spinal muscular atrophySuzie Lefebvre, Philippe Burlet, Louis Viollet, et al.
Scientific Reports|October 22, 2020
Reconstructing the hydraulics of the world's first industrial complex, the second century CE Barbegal watermills, FranceCees W Passchier, Marcel Bourgeois, Pierre-Louis Viollet, et al.
Brain : a Journal of Neurology|August 26, 2003
Dominant and recessive central core disease associated with RYR1 mutations and fetal akinesiaNorma Beatriz Romero, Nicole Monnier, Louis Viollet, et al.
British Journal of Clinical Pharmacology|February 3, 2011
Riluzole pharmacokinetics in young patients with spinal muscular atrophyChadi Abbara, Brigitte Estournet, Lucette Lacomblez, et al.
Journal of Neuromuscular Diseases|November 19, 2016
Orthopedic Management of Scoliosis by Garches Brace and Spinal Fusion in SMA Type 2 ChildrenMichela Catteruccia, Carole Vuillerot, Isabelle Vaugier, et al.
American Journal of Human Genetics|June 15, 2007
The nuclear factor kappaB-activator gene PLEKHG5 is mutated in a form of autosomal recessive lower motor neuron disease with childhood onsetIsabelle Maystadt, René Rezsöhazy, Martine Barkats, et al.
Pageof 3