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La ricerca find articoli where authors phrase all words ' Bouchard, JP' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 52 riferimenti
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    1. Yoshino, H; Lemaitre, A; Bouchard, JP
      Multiple domain growth and memory in the droplet model for spin-glasses

      EUROPEAN PHYSICAL JOURNAL B
    2. Dupre, N; Cossette, L; Hand, CK; Bouchard, JP; Rouleau, GA; Puymirat, J
      A founder mutation in French-Canadian families with X-linked hereditary neuropathy

      CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES
    3. Jonason, K; Nordblad, P; Vincent, E; Hammann, J; Bouchard, JP
      Memory interference effects in spin glasses

      EUROPEAN PHYSICAL JOURNAL B
    4. Engert, JC; Berube, P; Mercier, J; Dore, C; Lepage, P; Ge, B; Bouchard, JP; Mathieu, J; Melancon, SB; Schalling, M; Lander, ES; Morgan, K; Hudson, TJ; Richter, A
      ARSACS, a spastic ataxia common in northeastern Quebec, is caused by mutations in a new gene encoding an 11.5-kb ORF

      NATURE GENETICS
    5. Blumen, SC; Korczyn, AD; Lavoie, H; Medynski, S; Chapman, J; Asherov, A; Nisipeanu, P; Inzelberg, R; Carasso, RL; Bouchard, JP; Tome, FMS; Rouleau, GA; Brais, B
      Oculopharyngeal MD among Bukhara Jews is due to a founder (GCG)9 mutation in the PABP2 gene

      NEUROLOGY
    6. Bouchard, JP; Tetu, M; Janz, S; Xu, DX; Wasilewski, ZR; Piva, P; Akano, UG; Mitchell, IV
      Quasi-phase matched second-harmonic generation in an AlxGa1-xAs asymmetricquantum-well waveguide using ion-implantation-enhanced intermixing

      APPLIED PHYSICS LETTERS
    7. Blumen, SC; Brais, B; Korczyn, AD; Medinsky, S; Chapman, J; Asherov, A; Nisipeanu, P; Codere, F; Bouchard, JP; Fardeau, M; Tome, FMS; Rouleau, GA
      Homozygotes for oculopharyngeal muscular dystrophy have a severe form of the disease

      ANNALS OF NEUROLOGY
    8. Dupre, N; Bouchard, JP; Cossette, L; Brunet, D; Vanasse, M; Lemieux, B; Mathon, G; Puymirat, J
      Clinical and electrophysiological study in French-Canadian population withCharcot-Marie-Tooth disease type 1A associated with 17p11.2 duplication

      CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES
    9. Brais, B; Rouleau, GA; Bouchard, JP; Fardeau, M; Tome, FMS
      Oculopharyngeal muscular dystrophy

      SEMINARS IN NEUROLOGY
    10. Ebers, G; Lee, D; Rice, G; Lesaux, J; Kennedy, K; Sanders, EACM; Versteylen, RJ; van Andel, JD; Story, JP; de Milliano, M; O'Connor, P; Cheung, G; Houston, P; Hall, J; Comi, G; Filippi, M; Martinelli, V; Santuccio, G; Poggi, A; Gironi, M; Moiola, L; Duquette, P; Bourgouin, P; Pepin, G; Poirer, J; Bernier, G; Dubois, R; Metz, L; Diamond, RT; Bell, R; McGowan, D; Demchuk, A; Harris, E; Yeung, M; Murphy, A; Murray, TJ; Vandorpe, R; Bhan, V; Maxner, C; Weldon, P; Armstrong, L; Bouchard, JP; Grondin, P; Gosselin, F; Thibaut, M; Kirouac, L; Morin, A; Abramsky, O; Gomori, JM; Karussis, D; Karni, A; Mor, M; Freedman, MS; Avruch, L; Nelson, R; Christie, S; Rabinovitch, H; Freedman, C; Benavente, M; Pelletier, J; Levrier, O; Bensa, P; Dalesky, A; Paty, D; Li, D; Rhodes, B; Riddehough, A; Zhao, G; Wang, X; Chang, Y; Abdul-Ahad, A; Ammoury, N; Dupont, F; Francis, G; Furcha, R; Galazka, A; Hyde, R; Olson, M; Pernin, MO; Shah, S; Freedman, M; Ebers, G; Murray, J; O'Connor, P; Paty, D; Rice, G; Francis, G
      Evidence of interferon beta-1a dose response in relapsing-remitting MS - The OWIMS study

      NEUROLOGY
    11. Arnason, BGW; Jacobs, G; Hanlon, M; Clay, BH; Noronha, ABC; Auty, A; Davis, B; Nath, A; Bouchard, JP; Belanger, C; Gosselin, F; Thibault, M; Duquette, P; Bourgoin, P; DuBois, R; Girard, M; Ebers, GC; Rice, GPA; Vandervoort, MK; Francis, GS; Duncan, L; Lapierre, Y; Freedman, MS; Christie, SN; Rabinovitch, HE; Patry, D; Murphy, WF; Peters, S; McGuiness, SD; Murray, TJ; Bhan, V; Maxner, CE; Van Dorpe, R; Oger, JJ; Nelson, J; Morrison, W; Bogle, N; Beall, S; Vorobeychick, G; Hiltbrunner, AV; Bock, J; Habil; Lesslauer, W; Li, DKB; Paty, DW; Zhao, GJ
      TNF neutralization in MS - Results of a randomized, placebo-controlled multicenter study

      NEUROLOGY
    12. Skuk, D; Furling, D; Bouchard, JP; Goulet, M; Roy, B; Lacroix, Y; Vilquin, JT; Tremblay, JP; Puymirat, J
      Transplantation of human myoblasts in SCID mice as a potential muscular model for myotonic dystrophy

      JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
    13. Richter, A; Rioux, JD; Bouchard, JP; Mercier, J; Mathieu, J; Ge, B; Poirier, J; Julien, D; Gyapay, G; Weissenbach, J; Hudson, TJ; Melancon, SB; Morgan, K
      Location score and haplotype analyses of the locus for autosomal recessivespastic ataxia of Charlevoix-Saguenay, in chromosome region 13q11

      AMERICAN JOURNAL OF HUMAN GENETICS
    14. BRAIS B; BOUCHARD JP; XIE YG; ROCHEFORT DL; CHRETIEN N; TOME FMS; LAFRENIERE RG; ROMMENS JM; UYAMA E; NOHIRA O; BLUMEN S; KORCYN AD; HEUTINK P; MATHIEU J; DURANCEAU A; CODERE F; FARDEAU M; ROULEAU GA
      SHORT GCG EXPANSIONS IN THE PABP2 GENE CAUSE OCULOPHARYNGEAL MUSCULAR-DYSTROPHY

      Nature genetics
    15. HOWARD HC; DUBE MP; PREVOST C; LOPESCENDES I; CASAUBON LK; MELANSON M; ANDERMANN E; ANDERMANN F; BOUCHARD JP; MATHIEU J; ROULEAU GA
      THE CANDIDATE INTERVAL FOR PERIPHERAL NEUROPATHY WITH OR WITHOUT AGENESIS OF THE CORPUS-CALLOSUM MAPS TO A 1 CM REGION ON CHROMOSOME 15Q

      European journal of human genetics
    16. BOUCHARD JP; RICHTER A; MATHIEU J; BRUNET D; HUDSON TJ; MORGAN K; MELANCON SB
      AUTOSOMAL RECESSIVE SPASTIC ATAXIA OF CHARLEVOIX-SAGUENAY

      Neuromuscular disorders
    17. BRAIS B; BOUCHARD JP; TOME FMS; FARDEAU M; CODERE F; DURANCEAU A; ROULEAU GA
      GENETIC-EVIDENCE FOR THE INVOLVEMENT OF OTHER GENES IN MODULATING THESEVERITY OF OCULOPHARYNGEAL MUSCULAR-DYSTROPHY

      Annals of neurology
    18. FURLING D; BOUCHARD JP; PUYMIRAT J
      DECREASED LEVELS IN MYOTONIN PROTEIN-KINASE IS ASSOCIATED WITH A DELAY IN HUMAN MYOTONIC-DYSTROPHY MYOBLAST DIFFERENTIATION

      Annals of neurology
    19. AUTY A; BELANGER C; BOUCHARD JP; BRUNET DG; DUQUETTE P; FRANCIS GS; FREEDMAN MS; HADER WJ; MARSHALL SC; MAXNER CE; METZ L; MURRAY TJ; OCONNOR P; OGER J; PAULSETH JE; PRYSEPHILLIPS WE; RICE GPA; ALCOCK G; AMAOUTELIS R; LEWIS P; ARMSTRONG L; BOUCHER D; DAVIS B; EDGER C; HISER D; LESAUX J; VANDERVOORT P; HADER M; MCGUINESS S; MORRISON W; NELSON J; PACK D; NEUFELD B; HAYNES JA; PERERA M; POIRIER J; STEVENSON K; RIVIERE M; TRETIAK R; BELANGER M; LAPLANTE S; GRENIER JF
      BURDEN OF ILLNESS OF MULTIPLE-SCLEROSIS - PART I - COST OF ILLNESS

      Canadian journal of neurological sciences
    20. AUTY A; BELANGER C; BOUCHARD JP; BRUNET DG; DUQUETTE P; FRANCIS GS; FREEDMAN MS; HADER WJ; MARSHALL SC; MAXNER CE; METZ L; MURRAY TJ; OCONNOR P; OGER J; PAULSETH JE; PRYSEPHILLIPS WE; RICE GPA; RITVO P; ALCOCK G; ARNAOUTELIS R; LEWIS P; ARMSTRONG L; BOUCHER D; DAVIS B; EDGAR C; HISER D; LESAUX J; VANDERVOORT P; HADER M; MCGUINESS S; MORRISON W; NELSON J; PACK D; NEUFELD B; HAYNES JA; PERERA M; POIRIER J; STEVENSON K; RIVIERE M; BRETON MC; BELANGER M; LAPLANTE S; GRENIER JF
      BURDEN OF ILLNESS OF MULTIPLE-SCLEROSIS - PART II - QUALITY-OF-LIFE

      Canadian journal of neurological sciences
    21. ETONGUEMAYER P; FAURE R; BOUCHARD JP; PUYMIRAT J
      CHARACTERIZATION OF A 54-KILODALTON HUMAN PROTEIN-KINASE RECOGNIZED BY AN ANTISERUM RAISED AGAINST THE MYOTONIN KINASE

      Muscle & nerve
    22. DOYON J; LAFORCE R; BOUCHARD G; GAUDREAU D; ROY J; POIRIER M; BEDARD PJ; BEDARD F; BOUCHARD JP
      ROLE OF THE STRIATUM, CEREBELLUM AND FRONTAL LOBES IN THE AUTOMATIZATION OF A REPEATED VISUOMOTOR SEQUENCE OF MOVEMENTS

      Neuropsychologia
    23. BOUCHARD JP
      DISCOVERY OF MULTIPLE-SCLEROSIS - NOSOGRAPHIC REASONING - FRENCH - YANACOPAULO,BA

      Canadian journal of public health
    24. BOUCHARD JP
      REPORT ON THE FIRST INTERNATIONAL-SYMPOSIUM ON OCULOPHARYNGEAL MUSCULAR-DYSTROPHY

      Neuromuscular disorders
    25. BOUCHARD JP
      BARBEAU,ANDRE AND THE OCULOPHARYNGEAL MUSCULAR-DYSTROPHY IN FRENCH-CANADA AND NORTH-AMERICA

      Neuromuscular disorders
    26. BOUCHARD JP; BRAIS B; BRUNET D; GOULD PV; ROULEAU GA
      RECENT STUDIES ON OCULOPHARYNGEAL MUSCULAR-DYSTROPHY IN QUEBEC

      Neuromuscular disorders
    27. MEOLA G; SANSONE V; ROTONDO G; TOME FMS; BOUCHARD JP
      OCULOPHARYNGEAL MUSCULAR-DYSTROPHY IN ITALY

      Neuromuscular disorders
    28. BRAIS B; BOUCHARD JP; GOSSELIN F; XIE YG; FARDEAU M; TOME FMS; ROULEAU GA
      USING THE FULL POWER OF LINKAGE ANALYSIS IN 11 FRENCH-CANADIAN FAMILIES TO FINE MAP THE OCULOPHARYNGEAL MUSCULAR-DYSTROPHY GENE

      Neuromuscular disorders
    29. FRADET G; POULIOT D; ROBICHAUD R; STPIERRE S; BOUCHARD JP
      UPPER ESOPHAGEAL SPHINCTER MYOTOMY IN OCULOPHARYNGEAL MUSCULAR-DYSTROPHY - LONG-TERM CLINICAL-RESULTS

      Neuromuscular disorders
    30. MATHIEU J; LAPOINTE G; BRASSARD A; TREMBLAY C; BRAIS B; ROULEAU GA; BOUCHARD JP
      A PILOT-STUDY ON UPPER ESOPHAGEAL SPHINCTER DILATATION FOR THE TREATMENT OF DYSPHAGIA IN PATIENTS WITH OCULOPHARYNGEAL MUSCULAR-DYSTROPHY

      Neuromuscular disorders
    31. MONTERMINI L; RICHTER A; MORGAN K; JUSTICE CM; JULIEN D; CASTELLOTTI B; MERCIER J; POIRIER J; CAPOZZOLI F; BOUCHARD JP; LEMIEUX B; MATHIEU J; VANASSE M; SENI MH; GRAHAM G; ANDERMANN F; ANDERMANN E; MELANCON SB; KEATS BJB; DIDONATO S; PANDOLFO M
      PHENOTYPIC VARIABILITY IN FRIEDREICH-ATAXIA - ROLE OF THE ASSOCIATED GAA TRIPLET REPEAT EXPANSION

      Annals of neurology
    32. DOYON J; GAUDREAU D; LAFORCE R; CASTONGUAY M; BEDARD PJ; BEDARD F; BOUCHARD JP
      ROLE OF THE STRIATUM, CEREBELLUM, AND FRONTAL LOBES IN THE LEARNING OF A VISUOMOTOR SEQUENCE

      Brain and cognition
    33. EBERS GC; KUKAY K; BULMAN DE; SADOVNICK AD; RICE G; ANDERSON C; ARMSTRONG H; COUSIN K; BELL RB; HADER W; PATY DW; HASHIMOTO S; OGER J; DUQUETTE P; WARREN S; GRAY T; OCONNOR P; NATH A; AUTY A; METZ L; FRANCIS G; PAULSETH JE; MURRAY TJ; PRYSEPHILLIPS W; NELSON R; FREEDMAN M; BRUNET D; BOUCHARD JP; HINDS D; RISCH N
      A FULL GENOME SEARCH IN MULTIPLE-SCLEROSIS

      Nature genetics
    34. RICHTER A; POIRIER J; MERCIER J; JULIEN D; MORGAN K; ROY M; GOSSELIN F; BOUCHARD JP; MELANCON SB
      FRIEDREICH ATAXIA IN ACADIAN FAMILIES FROM EASTERN CANADA - CLINICAL DIVERSITY WITH CONSERVED HAPLOTYPES

      American journal of medical genetics
    35. LACOMBLEZ L; BENSIMON G; LEIGH PN; GUILLET P; POWE L; DURRLEMAN S; DELUMEAU JC; MEININGER V; PUECH AJ; WHITEHEAD J; ASSELAIN B; CESARO P; LARREY D; ROSSOR M; ZIMMERMAN HJ; SALZMAN P; DOPPLER V; LLOYD CM; MALOTEAUX JM; DELWAIDE C; LATERRE EC; BOUCHARD JP; DUQUETTE P; GIRARD M; MASSE C; EISEN A; BLIN O; AZULAY JP; BILLETURC F; POUGET J; BOUCHE P; CAMU M; CARLANDER B; BILLIARD M; CLANET M; ANGIBAUD G; ARNEBES MC; BENAZET M; COURATIER P; VALLAT JM; DESNUELLE C; LAGUENY A; ELLIE E; DIB M; ROZIER A; SALACHAS F; VIADER F; DELAUNAY D; DENGLER R; KUTHER G; TROGER M; LUDOLPH A; BACHUS R; GERICKE C; PRZUNTEK H; LANGKAFEL M; SCHIMRIGK K; JOST WH; OSTERHAGE J; PRUDLO J; MORA J; CHAVERRI D; SAENZ E; JEFFERSON D; ORPE V; LANE RJM; ORRELL RW; BARBIE T; MITCHELL JD; KILSHAW J; PALL HS; GOODWIN M; SCHADY W; DUNCAN S; MOORE C; RICHARDS C; SHAW PJ; CHARI G; PICKERING B; SWASH M; HARATI Y; GOOCH CL; ECHOLS CW; MILLER RG; GELINAS DF; QUIEN A; MUNSTAT TL; THORNELL B; ROTHSTEIN JD; CLAWSON L; SUFIT R; CASEY P; DELUMEAU J; TRUFFINET P; DEBOVE C; ENFRIN P; HAMPTON G; MULLER F; NGUYEN T; ROTHFUSS D; SENECHAL A; SHU C; LESWELL P; WHITWORTH P; DEBOE M; DEBRUYCKERE M; FISHER W; KONIG M; VERDUGO L; DELOSTERREROS MS; DEAKIN D; GIGUERE M; ADAIR K; FRANCO M; SKARINSKY D; WEXLER M; PIZZATO M; LEDOUX L; CAMPAGNES E; HARTNETT M; BASTIEN P; BEJUIT R; KIM Y; LELANN L; LEROY F; PAPILLON C; ORVOENFRIJA E
      A CONFIRMATORY DOSE-RANGING STUDY OF RILUZOLE IN ALS

      Neurology
    36. MILLER RG; BOUCHARD JP; DUQUETTE P; EISEN A; GELINAS DF; HARATI Y; MUNSAT TL; POWE L; ROTHSTEIN J; SALZMAN P; SUFIT RL; GUILLET P; BENSIMON G; DELUMEAU JC; DURRLEMAN S; LACOMBLEZ L; LEIGH PN; MEININGER V; MALOTEAUX JM; DELWAIDE C; GIRARD M; MASSE C; BLIN O; AZULAY JP; BILLETURC F; POUGET J; BOUCHE P; CAMU W; CARLANDER B; CLANET M; ANGIBAUD G; ARNEBES MC; BENAZET M; COURATIER P; DESNUELLE C; LAGUENY A; ELLIE E; DIB M; ROZIER A; SALACHAS F; VIADER F; DELAUNAY D; DENGLER R; GUTHER G; TROGER M; LUDOLPH A; BACHUS R; GERICKE C; PRZUNTEK H; LANGKAFEL M; SCHIMRIGK K; JOST WH; OSTERHAGE J; PRUDLO J; MORA J; CHAVERRI D; SAENZ E; JEFFERSON D; ORPE V; LANE RJM; ORRELL RW; LLOYD CM; BARBIE T; MITCHELL JD; KILSHAW J; PALL HS; GOODWIN M; SCHADY W; DUNCAN S; MOORE C; RICKARDS C; SHAW PJ; PICKERING CB; SWASH M; GOOCH CL; ECHOLS CW; QUIEN A; THORNELL B; ROTHSTEIN JD; CLAWSON L; SUFIT R; CASEY P
      CLINICAL-TRIALS OF RILUZOLE IN PATIENTS WITH ALS

      Neurology
    37. BRAIS B; TOME FMS; FARDEAU M; XIE YG; ROULEAU GA; BOUCHARD JP
      THE NATURAL-HISTORY OF OCULOPHARYNGEAL MUSCULAR-DYSTROPHY BASED ON THE STUDY OF A LARGE COHORT OF FRENCH-CANADIAN MUTATION CARRIERS

      Neurology
    38. MELANSON M; CASAUBON L; LOPESCENDES I; MARINEAU C; ANDERMANN E; ANDERMANN F; WEISSENBACH J; MATHIEU J; BOUCHARD JP; PREVOST C; ROULEAU GA
      THE GENE RESPONSIBLE FOR ANDERMANN SYNDROME MAPS TO CHROMOSOME 15Q

      Neurology
    39. CASAUBON LK; MELANSON M; LOPESCENDES I; MARINEAU C; ANDERMANN E; ANDERMANN F; WEISSENBACH J; PREVOST C; BOUCHARD JP; MATHIEU J; ROULEAU GA
      THE GENE RESPONSIBLE FOR A SEVERE FORM OF PERIPHERAL NEUROPATHY AND AGENESIS OF THE CORPUS-CALLOSUM MAPS TO CHROMOSOME 15Q

      American journal of human genetics
    40. BRAIS B; XIE YG; SANSON M; MORGAN K; WEISSENBACH J; KORCZYN AD; BLUMEN SC; FARDEAU M; TOME FMS; BOUCHARD JP; ROULEAU GA
      THE OCULOPHARYNGEAL MUSCULAR-DYSTROPHY LOCUS MAPS TO THE REGION OF THE CARDIAC ALPHA-MYOSIN AND BETA-MYOSIN HEAVY-CHAIN GENES ON CHROMOSOME14Q11.2-Q13

      Human molecular genetics
    41. RIVEST D; BRUNET D; DESBIENS R; BOUCHARD JP
      C-5 RADICULOPATHY AS A MANIFESTATION OF GIANT-CELL ARTERITIS

      Neurology
    42. BRAIS B; BOUCHARD JP; XIE YG; TOME FMS; FARDEAU M; ROULEAU GA
      A MORE SEVERE FORM OF OCULOPHARYNGEAL MUSCULAR-DYSTROPHY (OPMD) IS DOCUMENTED IN A GENETICALLY PROVEN HOMOZYGOUS PATIENT

      Neurology
    43. PUYMIRAT J; ETONGUEMAYER P; CHAHINE M; TREMBLAY J; BOUCHARD JP
      IMMORTALIZATION OF HUMAN MUSCLE-CELLS - A MODEL SYSTEM FOR THE DERIVATION OF DYSTROPHIC HUMAN MUSCLE-CELLS

      American journal of human genetics
    44. BRAIS B; MORGAN K; XIE Y; TOME FMS; FARDEAU M; BOUCHARD JP; ROULEAU GA
      STRONG LINKAGE DISEQUILIBRIUM SUGGEST ONE FOUNDER MUTATION IS RESPONSIBLE FOR ALL CASES OF OCULOPHARYNGEAL MUSCULAR-DYSTROPHY (OPMD) IN THEFRENCH-CANADIAN POPULATION

      American journal of human genetics
    45. RICHTER A; BOUCHARD JP; MELANCON SB
      GENOTYPE-PHENOTYPE CORRELATION IN ACADIAN FRIEDREICHS ATAXIA (FRDA-ACAD)

      American journal of human genetics
    46. PUYMIRAT J; COSSETTE L; GOSSELIN F; BOUCHARD JP
      RED-BLOOD-CELL CU ZN SUPEROXIDE-DISMUTASE ACTIVITY IN SPORADIC AMYOTROPHIC-LATERAL-SCLEROSIS/

      Journal of the neurological sciences
    47. ETONGUEMAYER P; FAURE R; BOUCHARD JP; THIBAULT MC; PUYMIRAT J
      THE MYOTONIN-PROTEIN KINASE PHOSPHORYLATES TYROSINE RESIDUES IN NORMAL HUMAN SKELETAL-MUSCLE

      Biochemical and biophysical research communications
    48. BELLESISLES M; ROY R; DANSEREAU G; GOULET M; ROY B; BOUCHARD JP; TREMBLAY JP
      RAPID SELECTION OF DONOR MYOBLAST CLONES FOR MUSCULAR-DYSTROPHY THERAPY USING CELL-SURFACE EXPRESSION OF NCAM

      European journal of histochemistry
    49. TREMBLAY JP; MALOUIN F; ROY R; HUARD J; BOUCHARD JP; SATOH A; RICHARDS CL
      RESULTS OF A TRIPLE BLIND CLINICAL-STUDY OF MYOBLAST TRANSPLANTATIONSWITHOUT IMMUNOSUPPRESSIVE TREATMENT IN YOUNG BOYS WITH DUCHENNE MUSCULAR-DYSTROPHY

      Cell transplantation
    50. BRAIS B; ROULEAU GA; SANSON M; GOSSELIN F; BOUCHARD JP
      OCULOPHARYNGEAL MUSCULAR-DYSTROPHY REVISITED - DIAGNOSTIC-CRITERIA AND VARIABILITY IN PHENOTYPE

      Neurology
    51. BOUCHARD JP; DOYON J; MORIN G; BARUCH P
      COGNITIVE DEFICITS ASSOCIATED WITH MYASTHENIA-GRAVIS

      Neurology
    52. RICHARDS CL; MALOUIN F; WOODDAUPHINEE S; WILLIAMS JI; BOUCHARD JP; BRUNET D
      TASK-SPECIFIC PHYSICAL THERAPY FOR OPTIMIZATION OF GAIT RECOVERY IN ACUTE STROKE PATIENTS

      Archives of physical medicine and rehabilitation


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Documento generato il 04/08/20 alle ore 05:18:18