Cortelli P - Search Results

1

Does the prion protein gene 129 codon polymorphism influence sleep? Evidence from a fatal familial insomnia kindred.

Plazzi G, Montagna P, Beelke M, Nobili L, De Carli F, Cortelli P, Vandi S, Avoni P, Tinuper P, Gambetti P, Lugaresi E, Ferrillo F. Plazzi G, et al. Among authors: cortelli p. Clin Neurophysiol. 2002 Dec;113(12):1948-53. doi: 10.1016/s1388-2457(02)00308-5. Clin Neurophysiol. 2002. PMID: 12464332

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

Isolated failure of noradrenergic transmission in a case with orthostatic hypotension and hyperactivity of gastro-colic reflex.

Cortelli P, Parchi P, Contin M, Sforza E, Lugaresi A, Pasquali R, Lugaresi E. Cortelli P, et al. Clin Auton Res. 1992 Jun;2(3):177-82. doi: 10.1007/BF01818959. Clin Auton Res. 1992. PMID: 1323364

4

Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene.

Medori R, Tritschler HJ, LeBlanc A, Villare F, Manetto V, Chen HY, Xue R, Leal S, Montagna P, Cortelli P, et al. Medori R, et al. Among authors: cortelli p. N Engl J Med. 1992 Feb 13;326(7):444-9. doi: 10.1056/NEJM199202133260704. N Engl J Med. 1992. PMID: 1346338 Free PMC article.

5

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

6

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.

7

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

8

Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism.

Goldfarb LG, Petersen RB, Tabaton M, Brown P, LeBlanc AC, Montagna P, Cortelli P, Julien J, Vital C, Pendelbury WW, et al. Goldfarb LG, et al. Among authors: cortelli p. Science. 1992 Oct 30;258(5083):806-8. doi: 10.1126/science.1439789. Science. 1992. PMID: 1439789

9

Brain energy metabolism studied by 31P-MR spectroscopy in a case of migraine with prolonged aura.

Sacquegna T, Lodi R, De Carolis P, Tinuper P, Cortelli P, Zaniol P, Funicello R, Montagna P, Barbiroli B. Sacquegna T, et al. Among authors: cortelli p. Acta Neurol Scand. 1992 Oct;86(4):376-80. doi: 10.1111/j.1600-0404.1992.tb05104.x. Acta Neurol Scand. 1992. PMID: 1455984

10

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

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