Barbiroli B - Search Results

1

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

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

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

5

Phosphorus magnetic resonance spectroscopy in cluster headache.

Montagna P, Lodi R, Cortelli P, Pierangeli G, Iotti S, Cevoli S, Zaniol P, Barbiroli B. Montagna P, et al. Among authors: barbiroli b. Neurology. 1997 Jan;48(1):113-8. doi: 10.1212/wnl.48.1.113. Neurology. 1997. PMID: 9008505

6

Improved brain and muscle mitochondrial respiration with CoQ. An in vivo study by 31P-MR spectroscopy in patients with mitochondrial cytopathies.

Barbiroli B, Iotti S, Lodi R. Barbiroli B, et al. Biofactors. 1999;9(2-4):253-60. doi: 10.1002/biof.5520090221. Biofactors. 1999. PMID: 10416038

7

'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

8

Phosphorus MR spectroscopy shows a tissue specific in vivo distribution of biochemical expression of the G3460A mutation in Leber's hereditary optic neuropathy.

Lodi R, Carelli V, Cortelli P, Iotti S, Valentino ML, Barboni P, Pallotti F, Montagna P, Barbiroli B. Lodi R, et al. Among authors: barbiroli b. J Neurol Neurosurg Psychiatry. 2002 Jun;72(6):805-7. doi: 10.1136/jnnp.72.6.805. J Neurol Neurosurg Psychiatry. 2002. PMID: 12023431 Free PMC article.

9

In vivo evidence of neuronal loss in the hypothalamus of narcoleptic patients.

Lodi R, Tonon C, Vignatelli L, Iotti S, Montagna P, Barbiroli B, Plazzi G. Lodi R, et al. Among authors: barbiroli b. Neurology. 2004 Oct 26;63(8):1513-5. doi: 10.1212/01.wnl.0000142259.94107.4c. Neurology. 2004. PMID: 15505179

10

Free Mg2+ concentration in the calf muscle of glycogen phosphorylase and phosphofructokinase deficiency patients assessed in different metabolic conditions by 31P MRS.

Malucelli E, Lodi R, Martinuzzi A, Tonon C, Barbiroli B, Iotti S. Malucelli E, et al. Among authors: barbiroli b. Dyn Med. 2005 Jun 6;4:7. doi: 10.1186/1476-5918-4-7. Dyn Med. 2005. PMID: 15938748 Free PMC article.

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