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L Monari

Showing results (11-20 of 22) with videos related to

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Italian Journal of Neurological Sciences|August 10, 2000
Cerebellar ataxia, hypogonadism and chorioretinopathy: molecular analysis of an Italian familyR Rizzi, V Carelli, L Monari, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|February 13, 2001
Equine muscular dystrophy with myotoniaP Montagna, R Liguori, L Monari, et al.
Brain & Development|October 24, 2000
Sneddon syndrome, arylsulfatase A pseudodeficiency and impairment of cerebral white matterA Parmeggiani, A Posar, L B De Giorgi, et al.
Journal of the Neurological Sciences|December 16, 1998
Leber's Hereditary Optic Neuropathy (LHON) with 14484/ND6 mutation in a North African patientV Carelli, P Barboni, A Zacchini, et al.
Neurology|July 1, 1995
Defective brain and muscle energy metabolism shown by in vivo 31P magnetic resonance spectroscopy in nonaffected carriers of 11778 mtDNA mutationB Barbiroli, P Montagna, P Cortelli, et al.
Neurology|April 1, 1994
31P-magnetic resonance spectroscopy in migraine without auraP Montagna, P Cortelli, L Monari, et al.
Epilepsia|March 1, 1994
Arylsulfatase A pseudodeficiency and Lafora bodies in a patient with progressive myoclonic epilepsyP Tinuper, G Plazzi, L Monari, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 29, 1994
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphismL Monari, S G Chen, P Brown, et al.
Brain Pathology (Zurich, Switzerland)|July 21, 1998
Molecular pathology of fatal familial insomniaP Parchi, R B Petersen, S G Chen, 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.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Italian Journal of Neurological Sciences|August 10, 2000
Cerebellar ataxia, hypogonadism and chorioretinopathy: molecular analysis of an Italian familyR Rizzi, V Carelli, L Monari, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|February 13, 2001
Equine muscular dystrophy with myotoniaP Montagna, R Liguori, L Monari, et al.
Brain & Development|October 24, 2000
Sneddon syndrome, arylsulfatase A pseudodeficiency and impairment of cerebral white matterA Parmeggiani, A Posar, L B De Giorgi, et al.
Journal of the Neurological Sciences|December 16, 1998
Leber's Hereditary Optic Neuropathy (LHON) with 14484/ND6 mutation in a North African patientV Carelli, P Barboni, A Zacchini, et al.
Neurology|July 1, 1995
Defective brain and muscle energy metabolism shown by in vivo 31P magnetic resonance spectroscopy in nonaffected carriers of 11778 mtDNA mutationB Barbiroli, P Montagna, P Cortelli, et al.
Neurology|April 1, 1994
31P-magnetic resonance spectroscopy in migraine without auraP Montagna, P Cortelli, L Monari, et al.
Epilepsia|March 1, 1994
Arylsulfatase A pseudodeficiency and Lafora bodies in a patient with progressive myoclonic epilepsyP Tinuper, G Plazzi, L Monari, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 29, 1994
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphismL Monari, S G Chen, P Brown, et al.
Brain Pathology (Zurich, Switzerland)|July 21, 1998
Molecular pathology of fatal familial insomniaP Parchi, R B Petersen, S G Chen, 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.
Pageof 3