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Brain : a Journal of Neurology|November 10, 2001
Morvan's syndrome: peripheral and central nervous system and cardiac involvement with antibodies to voltage-gated potassium channelsR Liguori, A Vincent, L Clover, et al.
Annals of Neurology|March 11, 1999
Biochemical features of mtDNA 14484 (ND6/M64V) point mutation associated with Leber's hereditary optic neuropathyV Carelli, A Ghelli, L Bucchi, et al.
Cephalalgia : an International Journal of Headache|November 14, 1997
Endozepine stupor in childrenS Soriani, M Carrozzi, L De Carlo, et al.
Journal of the Neurological Sciences|May 1, 1997
Clinical and brain bioenergetics improvement with idebenone in a patient with Leber's hereditary optic neuropathy: a clinical and 31P-MRS studyP Cortelli, P Montagna, G Pierangeli, et al.
Neurology|January 26, 2005
Paroxysmal arousal in epilepsy associated with cingulate hyperperfusionR Vetrugno, M Mascalchi, A Vella, et al.
Neurology|June 1, 1997
Leber's hereditary optic neuropathy: biochemical effect of 11778/ND4 and 3460/ND1 mutations and correlation with the mitochondrial genotypeV Carelli, A Ghelli, M Ratta, et al.
Sleep|April 1, 1995
Daytime sleepiness and nasal continuous positive airway pressure therapy in obstructive sleep apnea syndrome patients: effects of chronic treatment and 1-night therapy withdrawalE Sforza, E Lugaresi
Epilepsia|January 1, 1991
Partial motor epilepsy with "negative myoclonus"F Cirignotta, E Lugaresi
Brain Pathology (Zurich, Switzerland)|July 21, 1998
Molecular pathology of fatal familial insomniaP Parchi, R B Petersen, S G Chen, 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.
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