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Journal of Neurology, Neurosurgery, and Psychiatry|May 23, 1998
REM sleep behaviour disorder differentiates pure autonomic failure from multiple system atrophy with autonomic failureG Plazzi, P Cortelli, P Montagna, et al.
Brain : a Journal of Neurology|April 29, 1998
Endozepine stupor. Recurring stupor linked to endozepine-4 accumulationE Lugaresi, P Montagna, P Tinuper, et al.
Annals of the Rheumatic Diseases|October 28, 2008
Endothelin and sex hormones modulate the fibronectin synthesis by cultured human skin scleroderma fibroblastsS Soldano, P Montagna, B Villaggio, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 23, 2002
Phosphorus MR spectroscopy shows a tissue specific in vivo distribution of biochemical expression of the G3460A mutation in Leber's hereditary optic neuropathyR Lodi, V Carelli, P Cortelli, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 19, 2004
The role of cardiac diseases in the comorbidity between migraine and strokeG Pierangeli, S Cevoli, S Zanigni, et al.
European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association for Cardio-Thoracic Surgery|January 1, 1995
Technical aspects and late functional results of gastroepiploic bypass grafting (400 cases)O Jegaden, A Eker, P Montagna, et al.
Acta Neurologica Scandinavica|October 1, 1992
Brain energy metabolism studied by 31P-MR spectroscopy in a case of migraine with prolonged auraT Sacquegna, R Lodi, P De Carolis, et al.
Neurology|August 1, 1991
Leber's hereditary optic neuropathy: genetic, biochemical, and phosphorus magnetic resonance spectroscopy study in an Italian familyP Cortelli, P Montagna, P Avoni, et al.
Neuroendocrinology|June 1, 1995
Dissociated 24-hour patterns of somatotropin and prolactin in fatal familial insomniaF Portaluppi, P Cortelli, P Avoni, 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.
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