Barbiroli B - Search Results

1

'Secondary' 4216/ND1 and 13708/ND5 Leber's hereditary optic neuropathy mitochondrial DNA mutations do not further impair in vivo mitochondrial oxidative metabolism when associated with the 11778/ND4 mitochondrial DNA mutation.

Lodi R, Montagna P, Cortelli P, Iotti S, Cevoli S, Carelli V, Barbiroli B. Lodi R, et al. Among authors: barbiroli b. Brain. 2000 Sep;123 ( Pt 9):1896-902. doi: 10.1093/brain/123.9.1896. Brain. 2000. PMID: 10960053

2

Defective mitochondrial adenosine triphosphate production in skeletal muscle from patients with dominant optic atrophy due to OPA1 mutations.

Lodi R, Tonon C, Valentino ML, Manners D, Testa C, Malucelli E, La Morgia C, Barboni P, Carbonelli M, Schimpf S, Wissinger B, Zeviani M, Baruzzi A, Liguori R, Barbiroli B, Carelli V. Lodi R, et al. Among authors: barbiroli b. Arch Neurol. 2011 Jan;68(1):67-73. doi: 10.1001/archneurol.2010.228. Epub 2010 Sep 13. Arch Neurol. 2011. PMID: 20837821

3

The ND1 gene of complex I is a mutational hot spot for Leber's hereditary optic neuropathy.

Valentino ML, Barboni P, Ghelli A, Bucchi L, Rengo C, Achilli A, Torroni A, Lugaresi A, Lodi R, Barbiroli B, Dotti M, Federico A, Baruzzi A, Carelli V. Valentino ML, et al. Among authors: barbiroli b. Ann Neurol. 2004 Nov;56(5):631-41. doi: 10.1002/ana.20236. Ann Neurol. 2004. PMID: 15505787

4

Deficit of in vivo mitochondrial ATP production in OPA1-related dominant optic atrophy.

Lodi R, Tonon C, Valentino ML, Iotti S, Clementi V, Malucelli E, Barboni P, Longanesi L, Schimpf S, Wissinger B, Baruzzi A, Barbiroli B, Carelli V. Lodi R, et al. Among authors: barbiroli b. Ann Neurol. 2004 Nov;56(5):719-23. doi: 10.1002/ana.20278. Ann Neurol. 2004. PMID: 15505825

5

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. Neurology. 1992 Jun;42(6):1209-14. doi: 10.1212/wnl.42.6.1209. Neurology. 1992. PMID: 1603349

6

Leber's hereditary optic neuropathy: genetic, biochemical, and phosphorus magnetic resonance spectroscopy study in an Italian family.

Cortelli P, Montagna P, Avoni P, Sangiorgi S, Bresolin N, Moggio M, Zaniol P, Mantovani V, Barboni P, Barbiroli B, et al. Cortelli P, et al. Among authors: barbiroli b. Neurology. 1991 Aug;41(8):1211-5. doi: 10.1212/wnl.41.8.1211. Neurology. 1991. PMID: 1866007

7

Lipoic (thioctic) acid increases brain energy availability and skeletal muscle performance as shown by in vivo 31P-MRS in a patient with mitochondrial cytopathy.

Barbiroli B, Medori R, Tritschler HJ, Klopstock T, Seibel P, Reichmann H, Iotti S, Lodi R, Zaniol P. Barbiroli B, et al. J Neurol. 1995 Jul;242(7):472-7. doi: 10.1007/BF00873552. J Neurol. 1995. PMID: 7595680

8

Defective brain and muscle energy metabolism shown by in vivo 31P magnetic resonance spectroscopy in nonaffected carriers of 11778 mtDNA mutation.

Barbiroli B, Montagna P, Cortelli P, Iotti S, Lodi R, Barboni P, Monari L, Lugaresi E, Frassineti C, Zaniol P. Barbiroli B, et al. Neurology. 1995 Jul;45(7):1364-9. doi: 10.1212/wnl.45.7.1364. Neurology. 1995. PMID: 7617199

9

Brain and muscle energy metabolism studied in vivo by 31P-magnetic resonance spectroscopy in NARP syndrome.

Lodi R, Montagna P, Iotti S, Zaniol P, Barboni P, Puddu P, Barbiroli B. Lodi R, et al. Among authors: barbiroli b. J Neurol Neurosurg Psychiatry. 1994 Dec;57(12):1492-6. doi: 10.1136/jnnp.57.12.1492. J Neurol Neurosurg Psychiatry. 1994. PMID: 7798979 Free PMC article. Clinical Trial.

10

Defective brain energy metabolism shown by in vivo 31P MR spectroscopy in 28 patients with mitochondrial cytopathies.

Barbiroli B, Montagna P, Martinelli P, Lodi R, Iotti S, Cortelli P, Funicello R, Zaniol P. Barbiroli B, et al. J Cereb Blood Flow Metab. 1993 May;13(3):469-74. doi: 10.1038/jcbfm.1993.61. J Cereb Blood Flow Metab. 1993. PMID: 8478405

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