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P P Pramstaller

Showing results (11-20 of 49) with videos related to

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Brain : a Journal of Neurology|January 1, 1997
Apraxia in Parkinson's disease, progressive supranuclear palsy, multiple system atrophy and neuroleptic-induced parkinsonismR C Leiguarda, P P Pramstaller, M Merello, et al.
European Journal of Neurology|August 22, 2008
Adapted Finnish Migraine-Specific Questionnaire for family studies (FMSQ(FS)): a validation study in two languagesM F Facheris, F D Vogl, S Hollmann, et al.
Annals of Neurology|September 28, 1998
Clinical and genetic evaluation of a family with a mixed dystonia phenotype from South TyrolC Klein, P P Pramstaller, C C Castellan, et al.
Der Nervenarzt|August 5, 2000
[Genetics of dystonia]C Klein, M Kann, B Kis, et al.
Neurology|June 27, 2002
Novel three-stage ascertainment method: prevalence of PD and parkinsonism in South Tyrol, ItalyB Kis, A Schrag, Y Ben-Shlomo, et al.
Neurology|March 13, 2002
Parkin mutations in a patient with hemiparkinsonism-hemiatrophy: a clinical-genetic and PET studyP P Pramstaller, G Künig, K Leenders, et al.
European Journal of Neurology|August 3, 2013
Association between restless legs syndrome and hypertension: a preliminary population-based study in South Tyrol, ItalyG Giannini, S Zanigni, R Melotti, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 1, 1995
Nerve conduction studies, skeletal muscle EMG, and sphincter EMG in multiple system atrophyP P Pramstaller, G K Wenning, S J Smith, et al.
Annals of Neurology|July 14, 2000
Neuronal loss in Onuf's nucleus in three patients with progressive supranuclear palsyT Scaravilli, P P Pramstaller, A Salerno, et al.
Neurology|November 21, 2007
Sensorimotor integration is abnormal in asymptomatic Parkin mutation carriers: a TMS studyT Bäumer, P P Pramstaller, H R Siebner, et al.
Pageof 5

Showing results (11-20 of 49) with videos related to

Sort By:
Pageof 5
Brain : a Journal of Neurology|January 1, 1997
Apraxia in Parkinson's disease, progressive supranuclear palsy, multiple system atrophy and neuroleptic-induced parkinsonismR C Leiguarda, P P Pramstaller, M Merello, et al.
European Journal of Neurology|August 22, 2008
Adapted Finnish Migraine-Specific Questionnaire for family studies (FMSQ(FS)): a validation study in two languagesM F Facheris, F D Vogl, S Hollmann, et al.
Annals of Neurology|September 28, 1998
Clinical and genetic evaluation of a family with a mixed dystonia phenotype from South TyrolC Klein, P P Pramstaller, C C Castellan, et al.
Der Nervenarzt|August 5, 2000
[Genetics of dystonia]C Klein, M Kann, B Kis, et al.
Neurology|June 27, 2002
Novel three-stage ascertainment method: prevalence of PD and parkinsonism in South Tyrol, ItalyB Kis, A Schrag, Y Ben-Shlomo, et al.
Neurology|March 13, 2002
Parkin mutations in a patient with hemiparkinsonism-hemiatrophy: a clinical-genetic and PET studyP P Pramstaller, G Künig, K Leenders, et al.
European Journal of Neurology|August 3, 2013
Association between restless legs syndrome and hypertension: a preliminary population-based study in South Tyrol, ItalyG Giannini, S Zanigni, R Melotti, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 1, 1995
Nerve conduction studies, skeletal muscle EMG, and sphincter EMG in multiple system atrophyP P Pramstaller, G K Wenning, S J Smith, et al.
Annals of Neurology|July 14, 2000
Neuronal loss in Onuf's nucleus in three patients with progressive supranuclear palsyT Scaravilli, P P Pramstaller, A Salerno, et al.
Neurology|November 21, 2007
Sensorimotor integration is abnormal in asymptomatic Parkin mutation carriers: a TMS studyT Bäumer, P P Pramstaller, H R Siebner, et al.
Pageof 5