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SHUDDERING ATTACKS IN CHILDREN; AN EARLY CLINICAL MANIFESTATION OF ESSENTIAL TREMOR.VANASSE M; BEDARD P; ANDERMANN F et al.1976; NEUROLOGY; U.S.A.; DA. 1976; VOL. 26; NO 11; PP. 1027-1030; BIBL. 17 REF.Article

COMPLICATIONS NEUROLOGIQUES DES MENINGITES BACTERIENNES, EN PHASE AIGUE, CHEZ L'ENFANT: ETUDE CLINIQUE ET NEURO-RADIOLOGIQUEVANASSE M; DUBE J; DELAGE G et al.1982; UNION MEDICALE DU CANADA; ISSN 0041-6959; CAN; DA. 1982; VOL. 111; NO 11; PP. 963-968; ABS. ENG; BIBL. 21 REF.Article

DECREASE IN THE RATE OF PROTEIN SYNTHESIS BY POLYSOMES FROM CULTURED FIBROBLASTS OF PATIENTS AND CARRIERS WITH DUCHENNE MUSCULAR DYSTROPHYBOULE M; VANASSE M; BRAKIER GINGRAS L et al.1979; CANAD. J. NEUROL. SCI.; CAN; DA. 1979; VOL. 6; NO 3; PP. 355-358; ABS. FRE; BIBL. 16 REF.Article

SYNDROME D'ADIE ASSOCIE A UNE HYPOHIDROSE SEGMENTAIRE. ETUDE CLINIQUE ET NEUROPHYSIOLOGIQUEVANASSE M; MOLINA NEGRO P; SAINT HILAIRE JM et al.1974; REV. NEUROL.; FR.; DA. 1974; VOL. 130; NO 5-6; PP. 237-244; ABS. ANGL.; BIBL. 17 REF.Serial Issue

TUMEURS CEREBRALES DE L'ENFANT EN MILIEU CANADIEN-FRANCAISRENEVEY F; AMYOT Y; GEOFFROY G et al.1979; CANAD. J. NEUROL. SCI.; CAN; DA. 1979; VOL. 6; NO 3; PP. 329-335; ABS. ENG; BIBL. 35 REF.Article

Pain and the Guillain-Barré syndrome in children under 6 years oldDANG KHOA NGUYEN; AGENARIOTI-BELANGER, S; VANASSE, M et al.The Journal of pediatrics. 1999, Vol 134, Num 6, pp 773-776, issn 0022-3476Article

Neurologic crises in hereditary tyrosinemiaMITCHELL, G; LAROCHELLE, J; KHAZAL PARADIS et al.The New England journal of medicine. 1990, Vol 322, Num 7, pp 432-437, issn 0028-4793Article

Genetic recombination events which position the Friedreich ataxia locus proximal to the D9S15/D9S5 linkage group on chromosome 9qCHAMBERLAIN, S; FARRALL, M; FUJITA, R et al.American journal of human genetics. 1993, Vol 52, Num 1, pp 99-109, issn 0002-9297Article

Evoked potential studies in Friedreich's ataxia and progressive early onset cerebellar ataxiaVANASSE, M; GARCIA-LARREA, L; NEUSCHWANDER, P et al.Canadian journal of neurological sciences. 1988, Vol 15, Num 3, pp 292-298, issn 0317-1671Article

Intermittent treatment of febrile convulsions with nitrazepamVANASSE, M; MASSON, P; GEOFFROY, G et al.Canadian journal of neurological sciences. 1984, Vol 11, Num 3, pp 377-379, issn 0317-1671Article

Effects of hyperbaric oxygen therapy on children with spastic diplegic cerebral palsy : a pilot projectMONTGOMERY, D; GOLDBERG, J; AMAR, M et al.Undersea & hyperbaric medicine. 1999, Vol 26, Num 4, pp 235-242, issn 1066-2936Article

Linkage disequilibrium analysis of childhoot-onset spinal muscular atrophy (SMA) in the French-Canadian populationSIMARD, L. R; PRESCOTT, G; ROCHETTE, C et al.Human molecular genetics (Print). 1994, Vol 3, Num 3, pp 459-463, issn 0964-6906Article

Myoblast transfer in Duchenne muscular dystrophyKARPATI, G; AJDUKOVIC, D; WATTERS, G. V et al.Annals of neurology. 1993, Vol 34, Num 1, pp 8-17, issn 0364-5134Article

Somatosensory evoked potentials and auditory brain-stem responses in congenital hypothyroidism. I: A longitudinal study before and after treatment in six infants detected in the neonatal periodLAUREAU, E; VANASSE, M; HEBERT, R et al.Electroencephalography and clinical neurophysiology. 1986, Vol 64, Num 6, pp 501-510, issn 0013-4694Article

BETA-AMINO ACID TRANSPORT SYSTEM IN FRIEDREICH'S ATAXIAMELANCON SB; GRIGNON B; LEDRU E et al.1980; CAN. J. NEUROL. SCI.; ISSN 0317-1671; CAN; DA. 1980; VOL. 7; NO 4; PP. 441-446; ABS. FRE; BIBL. 31 REF.Article

EMG and needle muscle biopsy studies in arthrogryposis multiplex congenitaSTREHL, E; VANASSE, M; BROCHU, P et al.Neuropediatrics. 1985, Vol 16, Num 4, pp 225-227, issn 0174-304XArticle

The Andermann syndrome: agenesis of the corpus callosum associated with mental retardation and progressive sensorimotor neuronopathyLARBRISSEAU, A; VANASSE, M; BROCHU, P et al.Canadian journal of neurological sciences. 1984, Vol 11, Num 2, pp 257-261, issn 0317-1671Article

PREMIERE OBSERVATION CANADIENNE D'UNE FUCOSIDOSELARBRISSEAU A; BROCHU P; NG YING KIN NMK et al.1978; UN. MED. CANADA; CAN; DA. 1978; VOL. 107; NO 10; PP. 968-980; (9 P.); BIBL. 37 REF.Article

SMNT and NAIP mutations in Canadian families with spinal muscular atrophy (SMA) : Genotype/phenotype correlations with disease severitySIMARD, L. R; ROCHETTE, C; SEMIONOV, A et al.American journal of medical genetics. 1997, Vol 72, Num 1, pp 51-58, issn 0148-7299Article

Linkage study of chronic childhood-onset spinal muscular atrophy (SMA): confirmation of close linkage to D5S39 in French Canadian familiesSIMARD, L. R; VANASSE, M; ROCHETTE, C et al.Genomics (San Diego, Calif.). 1992, Vol 14, Num 1, pp 188-190, issn 0888-7543Article

Deletions in the dystrophin gene : analysis of Duchenne and Becker muscular dystrophy pateints in QuebecSIMARD, L. R; GINGAS, F; DELVOYE, N et al.Human genetics. 1992, Vol 89, Num 4, pp 419-424, issn 0340-6717Article

Hyperammonemia-hyperornithinemia-homocitrullinuria syndrome : neurologic, ophthalmologic, and neuropsychologic examination of six patientsLEMAY, J. F; LAMBERT, M. A; ORQUIN, J et al.The Journal of pediatrics. 1992, Vol 121, Num 5, pp 725-730, issn 0022-3476, 1Article

Normal brainstem auditory evoked potentials in adult hypothyroidismVANASSE, M; FISCHER, C; BERHTEZENE, F et al.The Laryngoscope. 1989, Vol 99, Num 3, pp 302-306, issn 0023-852XArticle

Auditory brainstem response audiometry in congenitally hypothyroid children under early replacement therapyHEBERT, R; LAUREAU, E; VANASSE, M et al.Pediatric research. 1986, Vol 20, Num 6, pp 570-573, issn 0031-3998Article

A new autosomal recessive spastic ataxia associated with frequent white matter changes maps to 2q33-34THIFLAULT, I; RIOUX, M. F; BOUCHARD, J. P et al.Brain. 2006, Vol 129, pp 2332-2340, issn 0006-8950, 9 p., 9Article

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