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P Cortelli

Showing results (221-230 of 248) with videos related to

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Diabetic Medicine : a Journal of the British Diabetic Association|December 20, 2016
Validation of the Composite Autonomic Symptom Score 31 (COMPASS 31) for the assessment of symptoms of autonomic neuropathy in people with diabetesC Greco, F Di Gennaro, C D'Amato, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 19, 2004
Spontaneous low cerebrospinal pressure: a mini reviewD Grimaldi, E Mea, L Chiapparini, et al.
Science (New York, N.Y.)|December 20, 1996
Evidence for the conformation of the pathologic isoform of the prion protein enciphering and propagating prion diversityG C Telling, P Parchi, S J DeArmond, et al.
Neurology|November 18, 1998
Fatal familial insomnia in a new Italian kindredA Padovani, M D'Alessandro, P Parchi, et al.
Science (New York, N.Y.)|October 30, 1992
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphismL G Goldfarb, R B Petersen, M Tabaton, et al.
Molecular Neurobiology|April 1, 1994
A novel mechanism of phenotypic heterogeneity demonstrated by the effect of a polymorphism on a pathogenic mutation in the PRNP (prion protein gene)R B Petersen, L G Goldfarb, M Tabaton, et al.
Italian Journal of Neurological Sciences|December 31, 1997
Searching for migraine genes: exclusion of 290 cM out of the whole human genomeL Monari, M Mochi, M L Valentino, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 28, 2010
Autonomic innervation in multiple system atrophy and pure autonomic failureV Donadio, P Cortelli, M Elam, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 19, 2004
Does headache represent a clinical marker in early diagnosis of cerebral venous thrombosis? A prospective multicentric studyS Iurlaro, E Beghi, N Massetto, et al.
Brain Pathology (Zurich, Switzerland)|July 21, 1998
Clinical features of fatal familial insomnia: phenotypic variability in relation to a polymorphism at codon 129 of the prion protein geneP Montagna, P Cortelli, P Avoni, et al.
Pageof 25

Showing results (221-230 of 248) with videos related to

Sort By:
Pageof 25
Diabetic Medicine : a Journal of the British Diabetic Association|December 20, 2016
Validation of the Composite Autonomic Symptom Score 31 (COMPASS 31) for the assessment of symptoms of autonomic neuropathy in people with diabetesC Greco, F Di Gennaro, C D'Amato, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 19, 2004
Spontaneous low cerebrospinal pressure: a mini reviewD Grimaldi, E Mea, L Chiapparini, et al.
Science (New York, N.Y.)|December 20, 1996
Evidence for the conformation of the pathologic isoform of the prion protein enciphering and propagating prion diversityG C Telling, P Parchi, S J DeArmond, et al.
Neurology|November 18, 1998
Fatal familial insomnia in a new Italian kindredA Padovani, M D'Alessandro, P Parchi, et al.
Science (New York, N.Y.)|October 30, 1992
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphismL G Goldfarb, R B Petersen, M Tabaton, et al.
Molecular Neurobiology|April 1, 1994
A novel mechanism of phenotypic heterogeneity demonstrated by the effect of a polymorphism on a pathogenic mutation in the PRNP (prion protein gene)R B Petersen, L G Goldfarb, M Tabaton, et al.
Italian Journal of Neurological Sciences|December 31, 1997
Searching for migraine genes: exclusion of 290 cM out of the whole human genomeL Monari, M Mochi, M L Valentino, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 28, 2010
Autonomic innervation in multiple system atrophy and pure autonomic failureV Donadio, P Cortelli, M Elam, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 19, 2004
Does headache represent a clinical marker in early diagnosis of cerebral venous thrombosis? A prospective multicentric studyS Iurlaro, E Beghi, N Massetto, et al.
Brain Pathology (Zurich, Switzerland)|July 21, 1998
Clinical features of fatal familial insomnia: phenotypic variability in relation to a polymorphism at codon 129 of the prion protein geneP Montagna, P Cortelli, P Avoni, et al.
Pageof 25