Réformer l'expertise psychiatrique et l'expertise psychologique : un impératif pour la justiceBOUCHARD, Jean-Pierre.Concours médical (Paris). 2006, Vol 128, Num 2, pp 97-99, issn 0010-5309, 3 p.Article

La modélisation physique en hydrobiologie : conception des ouvrages de franchissement pour poissons migrateurs : Modèles physiques pour le XXI siècle = Scale modelling and hydrobiology: the design of fish passes : Physical modelling for XXI centuryBOUCHARD, Jean-Pierre.Houille blanche (Grenoble). 2004, Num 3, issn 0018-6368, 4, 57-64 [9 p.]Conference Paper

Paranoìa, schizophrénie, délires de persécution et dangerositéBOUCHARD, Jean-Pierre.Soins. Psychiatrie. 2010, Num 268, pp 38-42, issn 0241-6972, 5 p.Article

Intérêt curatif et préventif des thérapies cognitives et comportementales (TCC) dans le traitement de croyances délirantes schizophréniques criminogènes: TCC d'une conviction délirante ayant généré un double homicide à l'extérieur de la famille = The curative and preventative interest of cognitive behavioural therapy (CBT) in the treatment of delusional schizophrenic criminogenic beliefs: CBT of a delusional conviction that generated a double homicide outside the patient's familyBOUCHARD, Jean-Pierre.Annales médico-psychologiques. 2014, Vol 172, Num 9, pp 741-750, issn 0003-4487, 10 p.Article

Efficacy and Tolerability of a 20-mg Dose of Methylphenidate for the Treatment of Daytime Sleepiness in Adult Patients With Myotonic Dystrophy Type 1: A 2-Center, Randomized, Double-Blind, Placebo-Controlled, 3-Week Crossover TrialPUYMIRAT, Jack; BOUCHARD, Jean-Pierre; MATHIEU, Jean et al.Clinical therapeutics. 2012, Vol 34, Num 5, pp 1103-1111, issn 0149-2918, 9 p.Article

Hereditary ataxia, spastic paraparesis and neuropathy in the French-Canadian populationDUPRE, Nicolas; BOUCHARD, Jean-Pierre; BRAIS, Bernard et al.Canadian journal of neurological sciences. 2006, Vol 33, Num 2, pp 149-157, issn 0317-1671, 9 p.Article

Une nouvelle forme d'ataxie récessive causée par des mutations du gène SYNE-1 = Mutations in SYNE-I lead to a newly discovered form of autosomal recessive cerebellar ataxiaDUPRE, Nicolas; BOUCHARD, Jean-Pierre; GROS-LOUIS, Francois et al.MS. Médecine sciences. 2007, Vol 23, Num 3, pp 261-262, issn 0767-0974, 2 p.Article

Spectroscopic Calibration Correlation of Field and Lab-Sized Fluorescence LIDAR SystemsDERY, Bernard; BUTEAU, Sylvie; SIMARD, Jean-Robert et al.IEEE transactions on geoscience and remote sensing. 2010, Vol 48, Num 9, pp 3580-3586, issn 0196-2892, 7 p.Article

Autosomal dominant primary lateral sclerosisDUPRE, Nicolas; VALDMANIS, Paul N; BOUCHARD, Jean-Pierre et al.Neurology. 2007, Vol 68, Num 14, pp 1156-1157, issn 0028-3878, 2 p.Article

Mutation screening of the ALS2 gene in sporadic and familial amyotrophic lateral sclerosisHAND, Collette K; DEVON, Rebecca S; GROS-LOUIS, Francois et al.Archives of neurology (Chicago). 2003, Vol 60, Num 12, pp 1768-1771, issn 0003-9942, 4 p.Article

A founder mutation in french-canadian families with X-linked hereditary neuropathyDUPRE, Nicolas; COSSETTE, Louise; HAND, Collette K et al.Canadian journal of neurological sciences. 2001, Vol 28, Num 1, pp 51-55, issn 0317-1671Article

Current Status of the EarthCARE BBR Detectors DevelopmentALLARD, Martin; MARTIN, Louis; PROULX, Christian et al.Proceedings of SPIE, the International Society for Optical Engineering. 2011, Vol 8176, issn 0277-786X, isbn 978-0-8194-8803-9, 81761E.1-81761E.10Conference Paper

Mutations in SYNE1 lead to a newly discovered form of autosomal recessive cerebellar ataxiaGROS-LOUIS, Francois; DUPRE, Nicolas; DION, Patrick et al.Nature genetics. 2007, Vol 39, Num 1, pp 80-85, issn 1061-4036, 6 p.Article

Hereditary motor and sensory neuropathy with agenesis of the corpus callosumDUPRE, Nicolas; HOWARD, Heidi C; MATHIEU, Jean et al.Annals of neurology. 2003, Vol 54, Num 1, pp 9-18, issn 0364-5134, 10 p.Article

A Novel Duplication Confirms the Involvement of 5q23.2 in Autosomal Dominant LeukodystrophyMEIJER, Inge A; SIMOES-LOPES, Ana A; ROULEAU, Guy A et al.Archives of neurology (Chicago). 2008, Vol 65, Num 11, pp 1496-1501, issn 0003-9942, 6 p.Article

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosisKABASHI, Edor; VALDMANIS, Paul N; PRADAT, Pierre-Francois et al.Nature genetics. 2008, Vol 40, Num 5, pp 572-574, issn 1061-4036, 3 p.Article

Consensus conference on vCJD screening of blood donors: report of the panelMCCULLOUGH, Jeffrey; ANDERSON, David; REINHARZ, Daniel et al.Transfusion (Philadelphia, PA). 2004, Vol 44, Num 5, pp 675-683, issn 0041-1132, 9 p.Article

Genetic susceptibility to MS : a second stage analysis in Canadian MS familiesDYMENT, David A; WILLER, Cristen J; KASTRUKOFF, Lorne et al.Neurogenetics (Oxford. Print). 2001, Vol 3, Num 3, pp 145-151, issn 1364-6745Article

Clinical and genetic study of autosomal recessive cerebellar ataxia type 1DUPRE, Nicolas; GROS-LOUIS, Francois; CHRESTIAN, Nicolas et al.Annals of neurology. 2007, Vol 62, Num 1, pp 93-98, issn 0364-5134, 6 p.Article

Three families with amyotrophic lateral sclerosis and frontotemporal dementia with evidence of linkage to chromosome 9pVALDMANIS, Paul N; DUPRE, Nicolas; BOUCHARD, Jean-Pierre et al.Archives of neurology (Chicago). 2007, Vol 64, Num 2, pp 240-245, issn 0003-9942, 6 p.Article

Frequency domain, time-resolved and spectroscopic investigations of photosensitizers encapsulated in liposomal phantomsMERMUT, Ozzy; BOUCHARD, Jean-Pierre; CORMIER, Jean-Francois et al.Proceedings of SPIE, the International Society for Optical Engineering. 2007, pp 66320P.1-66320P.9, issn 0277-786X, isbn 978-0-8194-6776-8, 1VolConference Paper

Dystrophin expression in muscles of duchenne muscular dystrophy patients after high-density injections of normal myogenic cellsSKUK, Daniel; GOULET, Marlyne; SENAY, Hélène et al.Journal of neuropathology and experimental neurology. 2006, Vol 65, Num 4, pp 371-386, issn 0022-3069, 16 p.Article

Psychologie et justice : paroles d'expertsRIZET, Clément; VIAUX, Jean-Luc; BOUCHARD, Jean-Pierre et al.Le journal des psychologues. 2006, Num 238, pp 22-49, 28 p.Article