Rossella Medori - Publications

Università di Bologna, Bologna, Italy 

20 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
1996 Barbiroli B, Medori R, Tritschler HJ, Iotti S, Lodi R, Zaniol P. Thioctic acid stimulates muscle ATP production in patients with type 2-diabetes and diabetic polyneuropathy. An in vivo phosphorus magnetic resonance spectroscopy study Diabetes Und Stoffwechsel. 5: 71-76.  0.492
1995 Collinge J, Palmer MS, Sidle KC, Gowland I, Medori R, Ironside J, Lantos P. Transmission of fatal familial insomnia to laboratory animals. Lancet. 346: 569-70. PMID 7658786 DOI: 10.1016/S0140-6736(95)91405-6  0.313
1995 Barbiroli B, Medori R, Tritschler HJ, Klopstock T, Seibel P, Reichmann H, Iotti S, Lodi R, Zaniol P. Lipoic (thioctic) acid increases brain energy availability and skeletal muscle performance as shown by in vivo 31P-MRS in a patient with mitochondrial cytopathy. Journal of Neurology. 242: 472-7. PMID 7595680 DOI: 10.1007/BF00873552  0.51
1994 Tritschler HJ, Packer L, Medori R. Oxidative stress and mitochondrial dysfunction in neurodegeneration. Biochemistry and Molecular Biology International. 34: 169-81. PMID 7849618  0.547
1993 Tritschler HJ, Medori R. Mitochondrial DNA alterations as a source of human disorders. Neurology. 43: 280-8. PMID 8437690 DOI: 10.1212/Wnl.43.2.280  0.583
1993 Medori R, Tritschler HJ. Prion protein gene analysis in three kindreds with fatal familial insomnia (FFI): codon 178 mutation and codon 129 polymorphism. American Journal of Human Genetics. 53: 822-7. PMID 8105681  0.675
1992 Manetto V, Medori R, Cortelli P, Montagna P, Tinuper P, Baruzzi A, Rancurel G, Hauw JJ, Vanderhaeghen JJ, Mailleux P. Fatal familial insomnia: clinical and pathologic study of five new cases. Neurology. 42: 312-9. PMID 1736158 DOI: 10.1212/Wnl.42.2.312  0.701
1992 Medori R, Tritschler HJ, Gambetti P. Production of single-stranded DNA for sequencing: an alternative approach. Biotechniques. 12: 346-50. PMID 1349213  0.496
1992 Medori R, Montagna P, Tritschler HJ, LeBlanc A, Cortelli P, Tinuper P, Lugaresi E, Gambetti P. Fatal familial insomnia: a second kindred with mutation of prion protein gene at codon 178. Neurology. 42: 669-70. PMID 1347910 DOI: 10.1212/Wnl.42.3.669  0.732
1992 Medori R, Tritschler HJ, LeBlanc A, Villare F, Manetto V, Chen HY, Xue R, Leal S, Montagna P, Cortelli P. Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene. The New England Journal of Medicine. 326: 444-9. PMID 1346338 DOI: 10.1056/Nejm199202133260704  0.559
1989 Medori R, Brooke MH, Waterston RH. Two dissimilar brothers with Becker's dystrophy have an identical genetic defect. Neurology. 39: 1493-6. PMID 2682349 DOI: 10.1212/WNL.39.11.1493  0.319
1989 Tinuper P, Montagna P, Medori R, Cortelli P, Zucconi M, Baruzzi A, Lugaresi E. The thalamus participates in the regulation of the sleep-waking cycle. A clinico-pathological study in fatal familial thalamic degeneration. Electroencephalography and Clinical Neurophysiology. 73: 117-23. PMID 2473878 DOI: 10.1016/0013-4694(89)90190-9  0.52
1988 Montagna P, Gallassi R, Medori R, Govoni E, Zeviani M, Di Mauro S, Lugaresi E, Andermann F. MELAS syndrome: characteristic migrainous and epileptic features and maternal transmission. Neurology. 38: 751-4. PMID 3362373 DOI: 10.1212/Wnl.38.5.751  0.49
1988 Medori R, Autilio-Gambetti L, Jenich H, Gambetti P. Changes in axon size and slow axonal transport are related in experimental diabetic neuropathy. Neurology. 38: 597-601. PMID 2451191 DOI: 10.1212/Wnl.38.4.597  0.477
1988 Medori R, Jenich H, Autilio-Gambetti L, Gambetti P. Experimental diabetic neuropathy: similar changes of slow axonal transport and axonal size in different animal models. The Journal of Neuroscience. 8: 1814-1821. DOI: 10.1523/Jneurosci.08-05-01814.1988  0.484
1987 Lugaresi A, Baruzzi A, Cacciari E, Cortelli P, Medori R, Montagna P, Tinuper P, Zucconi M, Roiter I, Lugaresi E. Lack of vegetative and endocrine circadian rhythms in fatal familial thalamic degeneration. Clinical Endocrinology. 26: 573-80. PMID 3665119 DOI: 10.1111/J.1365-2265.1987.Tb00812.X  0.575
1986 Lugaresi E, Montagna P, Baruzzi A, Cortelli P, Tinuper P, Zucconi M, Gambetti PL, Medori R. [Familial insomnia with a malignant course: a new thalamic disease]. Revue Neurologique. 142: 791-2. PMID 3823713  0.582
1986 Lugaresi E, Medori R, Montagna P, Baruzzi A, Cortelli P, Lugaresi A, Tinuper P, Zucconi M, Gambetti P. Fatal familial insomnia and dysautonomia with selective degeneration of thalamic nuclei. The New England Journal of Medicine. 315: 997-1003. PMID 3762620 DOI: 10.1056/Nejm198610163151605  0.666
1985 Medori R, Autilio-Gambetti L, Monaco S, Gambetti P. Experimental diabetic neuropathy: impairment of slow transport with changes in axon cross-sectional area. Proceedings of the National Academy of Sciences of the United States of America. 82: 7716-20. PMID 2415969 DOI: 10.1073/Pnas.82.22.7716  0.44
1984 Coccagna C, Cirignotta F, Zucconi M, Gerardi R, Medori R, Lugaresi E. A polygraphic study of one case of primary alveolar hypoventilation (Ondine's curse). Bulletin Europã©En De Physiopathologie Respiratoire. 20: 157-61. PMID 6722366  0.412
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