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A Quattrone

Showing results (121-130 of 273) with videos related to

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Clinical Neuropharmacology|February 1, 1996
Functional preservation of benzodiazepine receptors of the primary somatosensory cortex in Creutzfeldt-Jakob disease: a pharmacologic-evoked potential studyU Aguglia, R L Oliveri, A Gambardella, et al.
Annals of Neurology|August 1, 1997
Long-duration response to levodopa influences the pharmacodynamics of short-duration response in Parkinson's diseaseM Zappia, R Colao, R Montesanti, et al.
Archives of Gerontology and Geriatrics|July 20, 2001
Plasma levels of vitamin E in Parkinson's diseaseG Nicoletti, L Crescibene, M Scornaienchi, et al.
AJNR. American Journal of Neuroradiology|December 31, 2016
A Fully Automated, Atlas-Based Approach for Superior Cerebellar Peduncle Evaluation in Progressive Supranuclear Palsy PhenotypesG Nicoletti, M E Caligiuri, A Cherubini, et al.
European Journal of Clinical Pharmacology|January 1, 1989
Computer analysis of saccadic eye movements: assessment of two different carbamazepine formulationsG Tedeschi, G Casucci, S Allocca, et al.
European Journal of Neurology|July 27, 2004
A novel mutation (Thr116Ile) in the presenilin 1 gene in a patient with early-onset Alzheimer's diseaseV La Bella, M Liguori, R Cittadella, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 18, 2007
A novel founder mutation in the MFN2 gene associated with variable Charcot-Marie-Tooth type 2 phenotype in two families from Southern ItalyM Muglia, G Vazza, A Patitucci, et al.
Biochemical and Biophysical Research Communications|December 14, 1990
Transformation by ras oncogene induces nuclear shift of protein kinase CV Chiarugi, L Magnelli, F Pasquali, et al.
Neurophysiologie Clinique = Clinical Neurophysiology|November 14, 1997
Disappearance of periodic sharp wave complexes in Creutzfeldt-Jakob diseaseU Aguglia, A Gambardella, E Le Piane, et al.
Epilepsia|September 16, 1999
Emotion-induced myoclonic absence-like seizures in a patient with inv-dup(15) syndrome: a clinical, EEG, and molecular genetic studyU Aguglia, E Le Piane, A Gambardella, et al.
Pageof 28

Showing results (121-130 of 273) with videos related to

Sort By:
Pageof 28
Clinical Neuropharmacology|February 1, 1996
Functional preservation of benzodiazepine receptors of the primary somatosensory cortex in Creutzfeldt-Jakob disease: a pharmacologic-evoked potential studyU Aguglia, R L Oliveri, A Gambardella, et al.
Annals of Neurology|August 1, 1997
Long-duration response to levodopa influences the pharmacodynamics of short-duration response in Parkinson's diseaseM Zappia, R Colao, R Montesanti, et al.
Archives of Gerontology and Geriatrics|July 20, 2001
Plasma levels of vitamin E in Parkinson's diseaseG Nicoletti, L Crescibene, M Scornaienchi, et al.
AJNR. American Journal of Neuroradiology|December 31, 2016
A Fully Automated, Atlas-Based Approach for Superior Cerebellar Peduncle Evaluation in Progressive Supranuclear Palsy PhenotypesG Nicoletti, M E Caligiuri, A Cherubini, et al.
European Journal of Clinical Pharmacology|January 1, 1989
Computer analysis of saccadic eye movements: assessment of two different carbamazepine formulationsG Tedeschi, G Casucci, S Allocca, et al.
European Journal of Neurology|July 27, 2004
A novel mutation (Thr116Ile) in the presenilin 1 gene in a patient with early-onset Alzheimer's diseaseV La Bella, M Liguori, R Cittadella, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 18, 2007
A novel founder mutation in the MFN2 gene associated with variable Charcot-Marie-Tooth type 2 phenotype in two families from Southern ItalyM Muglia, G Vazza, A Patitucci, et al.
Biochemical and Biophysical Research Communications|December 14, 1990
Transformation by ras oncogene induces nuclear shift of protein kinase CV Chiarugi, L Magnelli, F Pasquali, et al.
Neurophysiologie Clinique = Clinical Neurophysiology|November 14, 1997
Disappearance of periodic sharp wave complexes in Creutzfeldt-Jakob diseaseU Aguglia, A Gambardella, E Le Piane, et al.
Epilepsia|September 16, 1999
Emotion-induced myoclonic absence-like seizures in a patient with inv-dup(15) syndrome: a clinical, EEG, and molecular genetic studyU Aguglia, E Le Piane, A Gambardella, et al.
Pageof 28