Jack Puymirat
- Formation
- à venir
Aucune offre active
Autres opportunités de carrière
- Axe principal
- Neurosciences
- Adresse
- 2705, boulevard Laurier, RC-9300
Québec (Québec)
CANADA G1V 4G2 - Téléphone
- +1 418-525-4444, poste 42186
- Télécopieur
- +1 418-654-2753
- Courriel
- Jack.Puymirat@crchul.ulaval.ca
Publications récentes (voir toutes les publications de ce chercheur)
Beaulieu D, Thebault P, Pelletier R, Chapdelaine P, Tarnopolsky M, Furling D, Puymirat J. Abnormal prostaglandin E2 production blocks myogenic differentiation in myotonic dystrophy. Neurobiology of disease,
2012. 45: 122-9
Hiba B, Richard N, Hebert LJ, Cote C, Nejjari M, Vial C, Bouhour F, Puymirat J, Janier M. Quantitative assessment of skeletal muscle degeneration in patients with myotonic dystrophy type 1 using MRI. Journal of magnetic resonance imaging : JMRI,
2011. Epub
Cote C, Hiba B, Hebert LJ, Vial C, Remec JF, Janier M, Puymirat J. MRI of tibialis anterior skeletal muscle in myotonic dystrophy type 1. The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques,
2011. 38: 112-8
Levesque E, Leclerc D, Puymirat J, Knoppers BM. Developing registries of volunteers: key principles to manage issues regarding personal information protection. Journal of medical ethics,
2010. 36: 712-4
Vignaud A, Ferry A, Huguet A, Baraibar M, Trollet C, Hyzewicz J, Butler-Browne G, Puymirat J, Gourdon G, Furling D. Progressive skeletal muscle weakness in transgenic mice expressing CTG expansions is associated with the activation of the ubiquitin-proteasome pathway. Neuromuscular disorders : NMD,
2010. 20: 319-25
Hebert LJ, Remec JF, Saulnier J, Vial C, Puymirat J. The use of muscle strength assessed with handheld dynamometers as a non-invasive biological marker in myotonic dystrophy type 1 patients: a multicenter study. BMC musculoskeletal disorders,
2010. 11: 72
Beffy P, Del Carratore R, Masini M, Furling D, Puymirat J, Masiello P, Simili M. Altered signal transduction pathways and induction of autophagy in human myotonic dystrophy type 1 myoblasts. The international journal of biochemistry & cell biology,
2010. 42: 1973-83
Pelletier R, Hamel F, Beaulieu D, Patry L, Haineault C, Tarnopolsky M, Schoser B, Puymirat J. Absence of a differentiation defect in muscle satellite cells from DM2 patients. Neurobiology of disease,
2009. 36: 181-90
Dupre N, Chrestian N, Bouchard JP, Rossignol E, Brunet D, Sternberg D, Brais B, Mathieu J, Puymirat J. Clinical, electrophysiologic, and genetic study of non-dystrophic myotonia in French-Canadians. Neuromuscular disorders : NMD,
2009. 19: 330-4
Puymirat J, Giguere Y, Mathieu J, Bouchard JP. Intergenerational contraction of the ctg repeats in 2 families with myotonic dystrophy type 1. Neurology,
2009. 73: 2126-7
