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Sleep|December 24, 1997
Motor overactivity and loss of motor circadian rhythm in fatal familial insomnia: an actigraphic studyG Plazzi, Y Schutz, P Cortelli, 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.Clinical Endocrinology|May 1, 1987
Lack of vegetative and endocrine circadian rhythms in fatal familial thalamic degenerationA Lugaresi, A Baruzzi, E Cacciari, et al.Annals of Neurology|May 1, 1992
Idiopathic recurring stupor: a case with possible involvement of the gamma-aminobutyric acid (GABA)ergic systemP Tinuper, P Montagna, P Cortelli, et al.Neurology|December 1, 1993
[18F]FDG PET in fatal familial insomnia: the functional effects of thalamic lesionsD Perani, P Cortelli, G Lucignani, et al.Journal of the Neurological Sciences|August 1, 1991
Muscle mitochondrial DNA deletion and 31P-NMR spectroscopy alterations in a migraine patientN Bresolin, P Martinelli, B Barbiroli, et al.Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society|March 1, 1991
Cardiovascular dysautonomia in fatal familial insomniaP Cortelli, P Parchi, M Contin, et al.FEBS Letters|October 3, 1994
Functional alterations of the mitochondrially encoded ND4 subunit associated with Leber's hereditary optic neuropathyM Degli Esposti, V Carelli, A Ghelli, et al.Pageof 61