Cortelli P - Search Results

1

Abnormal lactate after effort in healthy carriers of Leber's hereditary optic neuropathy.

Montagna P, Plazzi G, Cortelli P, Carelli V, Lugaresi E, Barboni P, Fiocchi M. Montagna P, et al. Among authors: cortelli p. J Neurol Neurosurg Psychiatry. 1995 May;58(5):640-1. doi: 10.1136/jnnp.58.5.640. J Neurol Neurosurg Psychiatry. 1995. PMID: 7745422 Free PMC article. No abstract available.

2

Idiopathic recurring stupor: a case with possible involvement of the gamma-aminobutyric acid (GABA)ergic system.

Tinuper P, Montagna P, Cortelli P, Avoni P, Lugaresi A, Schoch P, Bonetti EP, Gallassi R, Sforza E, Lugaresi E. Tinuper P, et al. Among authors: cortelli p. Ann Neurol. 1992 May;31(5):503-6. doi: 10.1002/ana.410310507. Ann Neurol. 1992. PMID: 1317696

3

Fatal familial insomnia: a second kindred with mutation of prion protein gene at codon 178.

Medori R, Montagna P, Tritschler HJ, LeBlanc A, Cortelli P, Tinuper P, Lugaresi E, Gambetti P. Medori R, et al. Among authors: cortelli p. Neurology. 1992 Mar;42(3 Pt 1):669-70. doi: 10.1212/wnl.42.3.669. Neurology. 1992. PMID: 1347910

4

Endogenous benzodiazepine receptor ligands in idiopathic recurring stupor.

Rothstein JD, Guidotti A, Tinuper P, Cortelli P, Avoni P, Plazzi G, Lugaresi E, Schoch P, Montagna P. Rothstein JD, et al. Among authors: cortelli p. Lancet. 1992 Oct 24;340(8826):1002-4. doi: 10.1016/0140-6736(92)93011-b. Lancet. 1992. PMID: 1357403 Free article.

5

Abnormal sympathetic skin responses in thalamic lesions.

Montagna P, Cortelli P, Avoni P, Marchello LP, Monari L, Tinuper P, Gambetti P, Lugaresi E. Montagna P, et al. Among authors: cortelli p. Electroencephalogr Clin Neurophysiol. 1992 Jun;85(3):225-7. doi: 10.1016/0168-5597(92)90137-z. Electroencephalogr Clin Neurophysiol. 1992. PMID: 1376682

6

Mitochondrial DNA analysis in Leber's hereditary optic neuropathy.

Barboni P, Mantovani V, Montagna P, Bragliani M, Cortelli P, Lugaresi E, Puddu P, Caramazza R. Barboni P, et al. Among authors: cortelli p. Ophthalmic Paediatr Genet. 1992 Dec;13(4):219-26. doi: 10.3109/13816819209105170. Ophthalmic Paediatr Genet. 1992. PMID: 1488222

7

Brain 31P-magnetic resonance spectroscopy in mitochondrial cytopathies.

Montagna P, Martinelli P, Cortelli P, Zaniol P, Lugaresi E, Barbiroli B. Montagna P, et al. Among authors: cortelli p. Ann Neurol. 1992 Apr;31(4):451-2. doi: 10.1002/ana.410310422. Ann Neurol. 1992. PMID: 1586148 No abstract available.

8

Abnormal brain and muscle energy metabolism shown by 31P magnetic resonance spectroscopy in patients affected by migraine with aura.

Barbiroli B, Montagna P, Cortelli P, Funicello R, Iotti S, Monari L, Pierangeli G, Zaniol P, Lugaresi E. Barbiroli B, et al. Among authors: cortelli p. Neurology. 1992 Jun;42(6):1209-14. doi: 10.1212/wnl.42.6.1209. Neurology. 1992. PMID: 1603349

9

Fatal familial insomnia: clinical and pathologic study of five new cases.

Manetto V, Medori R, Cortelli P, Montagna P, Tinuper P, Baruzzi A, Rancurel G, Hauw JJ, Vanderhaeghen JJ, Mailleux P, et al. Manetto V, et al. Among authors: cortelli p. Neurology. 1992 Feb;42(2):312-9. doi: 10.1212/wnl.42.2.312. Neurology. 1992. PMID: 1736158

10

Cardiovascular dysautonomia in fatal familial insomnia.

Cortelli P, Parchi P, Contin M, Pierangeli G, Avoni P, Tinuper P, Montagna P, Baruzzi A, Gambetti PL, Lugaresi E. Cortelli P, et al. Clin Auton Res. 1991 Mar;1(1):15-21. doi: 10.1007/BF01826053. Clin Auton Res. 1991. PMID: 1821660

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