Cortelli P - Search Results

1

High frequency of migraine-only patients negative for the 3243 A>G tRNALeu mtDNA mutation in two MELAS families.

Cevoli S, Pallotti F, La Morgia C, Valentino ML, Pierangeli G, Cortelli P, Baruzzi A, Montagna P, Carelli V. Cevoli S, et al. Among authors: cortelli p. Cephalalgia. 2010 Aug;30(8):919-27. doi: 10.1177/0333102409354654. Epub 2010 Mar 12. Cephalalgia. 2010. PMID: 20656703

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

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

4

Autonomic nervous system function in myotonic dystrophy.

Pierangeli G, Lugaresi A, Contin M, Martinelli P, Montagna P, Parchi P, Verlicchi A, Cortelli P. Pierangeli G, et al. Among authors: cortelli p. Ital J Neurol Sci. 1992 Oct;13(7):589-92. doi: 10.1007/BF02233402. Ital J Neurol Sci. 1992. PMID: 1428793

5

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

6

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

7

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

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

Autonomic nervous system function in migraine without aura.

Cortelli P, Pierangeli G, Parchi P, Contin M, Baruzzi A, Lugaresi E. Cortelli P, et al. Headache. 1991 Jul;31(7):457-62. doi: 10.1111/j.1526-4610.1991.hed3107457.x. Headache. 1991. PMID: 1774161 Review.

10

Circadian hormonal rhythms in two new cases of fatal familial insomnia.

Avoni P, Cortelli P, Montagna P, Tinuper P, Sforza E, Contin M, Parchi P, Pierangeli G, Maltoni P, Pavani A, et al. Avoni P, et al. Among authors: cortelli p. Acta Neurol (Napoli). 1991 Dec;13(6):574-6. Acta Neurol (Napoli). 1991. PMID: 1805556

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

654 results

Search Page

Filters