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La ricerca find articoli where authors phrase all words ' Gwinn-Hardy, K' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 17 riferimenti
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    1. Farrer, M; Chan, P; Chen, R; Tan, L; Lincoln, S; Hernandez, D; Forno, L; Gwinn-Hardy, K; Petrucelli, L; Hussey, J; Singleton, A; Tanner, C; Hardy, J; Langston, JW
      Lewy bodies and parkinsonism in families with parkin mutations

      ANNALS OF NEUROLOGY
    2. Morris, HR; Al-Sarraj, S; Schwab, C; Gwinn-Hardy, K; Perez-Tur, J; Wood, NW; Hardy, J; Lees, AJ; McGeer, PL; Daniel, SE; Steele, JC
      A clinical and pathological study of motor neurone disease on Guam

      BRAIN
    3. Gwinn-Hardy, K; Singleton, A; O'Suilleabhain, P; Boss, M; Nicholl, D; Adam, A; Hussey, J; Critchley, P; Hardy, J; Farrer, M
      Spinocerebellar ataxia type 3 phenotypically resembling Parkinson disease in a black family

      ARCHIVES OF NEUROLOGY
    4. Lewis, J; McGowan, E; Rockwood, J; Melrose, H; Nacharaju, P; Van Slegtenhorst, M; Gwinn-Hardy, K; Murphy, MP; Baker, M; Yu, X; Duff, K; Hardy, J; Corral, A; Lin, WL; Yen, SH; Dickson, DW; Davies, P; Hutton, M
      Neurofibrillary tangles, amyotrophy and progressive motor disturbance in mice expressing mutant (P301L) tau protein

      NATURE GENETICS
    5. Evidente, VGH; Adler, CH; Caviness, JN; Hentz, JG; Gwinn-Hardy, K
      Amantadine is beneficial in restless legs syndrome

      MOVEMENT DISORDERS
    6. Caviness, JN; Gwinn-Hardy, K; Adler, CH; Muenter, MD
      Electrophysical observations in hereditary parkinsonism-dementia with Lewybody pathology

      MOVEMENT DISORDERS
    7. Gwinn-Hardy, K; Chen, JY; Liu, HC; Liu, TY; Boss, M; Seltzer, W; Adam, A; Singleton, A; Koroshetz, W; Waters, C; Hardy, J; Farrer, M
      Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese

      NEUROLOGY
    8. Gwinn-Hardy, K; Mehta, ND; Farrer, M; Maraganore, D; Muenter, M; Yen, SH; Hardy, J; Dickson, DW
      Distinctive neuropathology revealed by alpha-synuclein antibodies in hereditary parkinsonism and dementia linked to chromosome 4p

      ACTA NEUROPATHOLOGICA
    9. Hardy, J; Gwinn-Hardy, K
      Neurodegenerative disease: a different view of diagnosis

      MOLECULAR MEDICINE TODAY
    10. Farrer, M; Gwinn-Hardy, K; Hutton, M; Hardy, J
      The genetics of disorders with synuclein pathology and parkinsonism

      HUMAN MOLECULAR GENETICS
    11. Farrer, M; Gwinn-Hardy, K; Muenter, M; DeVrieze, FW; Crook, R; Perez-Tur, J; Lincoln, S; Maraganore, D; Adler, C; Newman, S; MacElwee, K; McCarthy, P; Miller, C; Waters, C; Hardy, J
      A chromosome 4p haplotype segregating with Parkinson's disease and postural tremor

      HUMAN MOLECULAR GENETICS
    12. Lincoln, S; Vaughan, J; Wood, N; Baker, M; Adamson, J; Gwinn-Hardy, K; Lynch, T; Hardy, J; Farrer, M
      Low frequency of pathogenic mutations in the ubiquitin carboxyterminal hydrolase gene in familial Parkinson's disease

      NEUROREPORT
    13. Evidente, VGH; Gwinn-Hardy, K; Caviness, JN; Adler, CH
      Risperidone is effective in severe hemichorea/hemiballismus

      MOVEMENT DISORDERS
    14. Evidente, VGH; Adler, CH; Caviness, JN; Gwinn-Hardy, K
      A pilot study on the motor effects of rimantadine in Parkinson's disease

      CLINICAL NEUROPHARMACOLOGY
    15. Lincoln, S; Crook, R; Chartier-Harlin, MC; Gwinn-Hardy, K; Baker, M; Mouroux, V; Richard, F; Becquet, E; Amouyel, P; Destee, A; Hardy, J; Farrer, M
      No pathogenic mutations in the beta-synuclein gene in Parkinson's disease

      NEUROSCIENCE LETTERS
    16. Lincoln, S; Gwinn-Hardy, K; Goudreau, J; Chartier-Harlin, MC; Baker, M; Mouroux, V; Richard, F; Destee, A; Becquet, E; Amouyel, P; Lynch, T; Hardy, J; Farrer, M
      No pathogenic mutations in the persyn gene in Parkinson's disease

      NEUROSCIENCE LETTERS
    17. Gwinn-Hardy, K; Evidente, VGH; Waters, C; Muenter, MD; Hardy, J
      L-dopa slows the progression of familial parkinsonism

      LANCET


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 28/01/21 alle ore 07:00:28