Zobrazeno 1 - 10
of 95
pro vyhledávání: '"J.P. Bouchard"'
Publikováno v:
Cell Transplantation, Vol 2 (1993)
The effects of myoblast transplantations without an immunosuppressive treatment on muscle strength, and the formation of dystrophin-positive fibers was studied in five young boys with Duchenne muscular dystrophy (DMD) using a triple blind design. Inj
Externí odkaz:
https://doaj.org/article/7d08c7b013c94583a8d75d115e1ff87c
Autor:
Peter S. McPherson, Claude Prévost, J.P. Bouchard, Nicolas Dupré, Jean Mathieu, Antoine Duquette, J. Demers-Lamarche, I. Thiffault, Marie-Josée Dicaire, Geneviève Bernard, Laura Montermini, Martine Tétreault, A. Montpetit, Bernard Brais, Roxanne Larivière, Andrea Richter, Kalle Gehring, Jocelyne Mercier, K.N. Huang, Grant A. Mitchell
Publikováno v:
Europe PubMed Central
Background:The growing number of spastic ataxia of Charlevoix-Saguenay (SACS) gene mutations reported worldwide has broadened the clinical phenotype of autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS). The identification of Quebec A
This study compares the residual stress profiles generated by two different welding techniques (multi-pass and single pass welding) in 80 mm thick ferritic steel welds. As residual stresses in such thick welded steel specimens that are representative
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e26e846f8e52ae41423035393096a0f
http://oro.open.ac.uk/60380/1/1-s2.0-S0020768315004175-main.pdf
http://oro.open.ac.uk/60380/1/1-s2.0-S0020768315004175-main.pdf
A novel autosomal recessive limb-girdle muscular dystrophy with quadriceps atrophy maps to 11p13-p12
Autor:
Yves Robitaille, V. Khoury, J.P. Bouchard, Isabelle Thiffault, Jonathan Jarry, M. F. Rioux, Bernard Brais, L. Loisel, Martine Tétreault, V. Bolduc
Publikováno v:
Brain. 130:368-380
Limb-girdle muscular dystrophies (LGMD) are a heterogeneous group of pathologies. We have identified a cohort of 14 French-Canadian patients from eight different families displaying a novel form of LGMD with an autosomal recessive inheritance. These
Autor:
Florentina Moatar, Benoît Camenen, A. Latapie, André Paquier, Stéphane Rodrigues, J.P. Bouchard
Publikováno v:
CATENA
CATENA, Elsevier, 2014, 121, pp.1--12. ⟨10.1016/j.catena.2014.04.017⟩
CATENA, Elsevier, 2014, 121, pp.1--12. ⟨10.1016/j.catena.2014.04.017⟩
International audience; This paper describes an approach to assess channel changes of a long anthropogenised river (the Middle Loire River) over decadal timescales. Channel changes are evaluated along geomorphically homogeneous river reaches. The cla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1278c075fd0c1231a66ac9fc1ef23be1
https://hal.archives-ouvertes.fr/hal-02377297
https://hal.archives-ouvertes.fr/hal-02377297
Autor:
Kenneth Morgan, J.P. Bouchard, D Julien, J Poirier, M. Roy, Andrea Richter, Jocelyne Mercier, F Gosselin, Serge B. Melançon
Publikováno v:
American Journal of Medical Genetics. 64:594-601
The gene for Friedreich ataxia (FRDA), an autosomal-recessive neurodegenerative disease, remains elusive. The current candidate region of about 150 kb lies between loci FR2 and F8101 near the D9S15/D9S5 linkage group at 9q13-21.1. Linkage homogeneity
Autor:
J.P. Bouchard, Marie-Pierre Dubé, J. Mathieu, Erin K. O'Ferrall, Marie-Josée Dicaire, N. Al-Bustani, Nigel G. Laing, V. Bolduc, Bernard Brais, Talita C. Conte, B. Beland, Sylvie Provost, Phillipa J. Lamont, Martine Tétreault, R.T. Hepple, G. Ravenscroft, Myriam Srour
Publikováno v:
Neuromuscular Disorders. 24:875-876
Muscle mass and strength are variable traits in humans. Many French Canadians (FC) became international celebrities because of their exceptional strength. Though muscle hypertrophy has been associated in many mammals with myostatin mutations, to date
Autor:
Marie-France Rioux, Jonathan Jarry, Josée Poirier, Isabelle Thiffault, L. Loiselle, Martine Tétreault, J. Lesage, Guy A. Rouleau, Bernard Brais, Michel Vanasse, J.P. Bouchard, Jean Mathieu, F. Gros-Louis
Publikováno v:
Brain : a journal of neurology. 129(Pt 9)
Recessive ataxias are a heterogeneous group of diseases. We identified a group of 23 French–Canadian cases belonging to 17 families affected by an autosomal recessive spastic ataxia associated with frequent white matter changes. The fact that 59% o
Publikováno v:
Journal of Hydraulic Engineering
Journal of Hydraulic Engineering, American Society of Civil Engineers, 2005, 131 (7), pp.586-595. ⟨10.1061/(ASCE)0733-9429(2005)131:7(586)⟩
Journal of Hydraulic Engineering, American Society of Civil Engineers, 2005, 131 (7), pp.586-595. ⟨10.1061/(ASCE)0733-9429(2005)131:7(586)⟩
International audience; Within inshore or fluvial environments, submerged fine matter mud banks are characterized by a high water content, a great spatial variability, and a strong deformability. The study of their instabilities induced by the variat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93f6bf53830eaedbf817e4d781be2a61
https://hal.archives-ouvertes.fr/hal-01007253
https://hal.archives-ouvertes.fr/hal-01007253
Publikováno v:
Neuromuscular Disorders. 21:717-718