Montagna P - Search Results

1

Ocular findings in mitochondrial neurogastrointestinal encephalomyopathy: a case report.

Barboni P, Savini G, Plazzi G, Bellan M, Valentino ML, Zanini M, Montagna P, Hirano M, Carelli V. Barboni P, et al. Among authors: montagna p. Graefes Arch Clin Exp Ophthalmol. 2004 Oct;242(10):878-80. doi: 10.1007/s00417-004-0914-y. Epub 2004 Mar 24. Graefes Arch Clin Exp Ophthalmol. 2004. PMID: 15042378

2

Retinal nerve fiber layer evaluation by optical coherence tomography in Leber's hereditary optic neuropathy.

Barboni P, Savini G, Valentino ML, Montagna P, Cortelli P, De Negri AM, Sadun F, Bianchi S, Longanesi L, Zanini M, de Vivo A, Carelli V. Barboni P, et al. Among authors: montagna p. Ophthalmology. 2005 Jan;112(1):120-6. doi: 10.1016/j.ophtha.2004.06.034. Ophthalmology. 2005. PMID: 15629831

3

Retinal nerve fiber layer evaluation by optical coherence tomography in unaffected carriers with Leber's hereditary optic neuropathy mutations.

Savini G, Barboni P, Valentino ML, Montagna P, Cortelli P, De Negri AM, Sadun F, Bianchi S, Longanesi L, Zanini M, Carelli V. Savini G, et al. Among authors: montagna p. Ophthalmology. 2005 Jan;112(1):127-31. doi: 10.1016/j.ophtha.2004.09.033. Ophthalmology. 2005. PMID: 15629832

4

Mitochondrial neurogastrointestinal encephalomyopathy: evidence of mitochondrial DNA depletion in the small intestine.

Giordano C, Sebastiani M, Plazzi G, Travaglini C, Sale P, Pinti M, Tancredi A, Liguori R, Montagna P, Bellan M, Valentino ML, Cossarizza A, Hirano M, d'Amati G, Carelli V. Giordano C, et al. Among authors: montagna p. Gastroenterology. 2006 Mar;130(3):893-901. doi: 10.1053/j.gastro.2006.01.004. Gastroenterology. 2006. PMID: 16530527

5

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: montagna p. Cephalalgia. 2010 Aug;30(8):919-27. doi: 10.1177/0333102409354654. Epub 2010 Mar 12. Cephalalgia. 2010. PMID: 20656703

6

Melanopsin retinal ganglion cells are resistant to neurodegeneration in mitochondrial optic neuropathies.

La Morgia C, Ross-Cisneros FN, Sadun AA, Hannibal J, Munarini A, Mantovani V, Barboni P, Cantalupo G, Tozer KR, Sancisi E, Salomao SR, Moraes MN, Moraes-Filho MN, Heegaard S, Milea D, Kjer P, Montagna P, Carelli V. La Morgia C, et al. Among authors: montagna p. Brain. 2010 Aug;133(Pt 8):2426-38. doi: 10.1093/brain/awq155. Epub 2010 Jul 21. Brain. 2010. PMID: 20659957 Free PMC article.

7

Association of optic disc size with development and prognosis of Leber's hereditary optic neuropathy.

Ramos Cdo V, Bellusci C, Savini G, Carbonelli M, Berezovsky A, Tamaki C, Cinoto R, Sacai PY, Moraes-Filho MN, Miura HM, Valentino ML, Iommarini L, De Negri AM, Sadun F, Cortelli P, Montagna P, Salomao SR, Sadun AA, Carelli V, Barboni P. Ramos Cdo V, et al. Among authors: montagna p. Invest Ophthalmol Vis Sci. 2009 Apr;50(4):1666-74. doi: 10.1167/iovs.08-2695. Epub 2008 Dec 20. Invest Ophthalmol Vis Sci. 2009. PMID: 19098324

8

The 13042G --> A/ND5 mutation in mtDNA is pathogenic and can be associated also with a prevalent ocular phenotype.

Valentino ML, Barboni P, Rengo C, Achilli A, Torroni A, Lodi R, Tonon C, Barbiroli B, Fortuna F, Montagna P, Baruzzi A, Carelli V. Valentino ML, et al. Among authors: montagna p. J Med Genet. 2006 Jul;43(7):e38. doi: 10.1136/jmg.2005.037507. J Med Genet. 2006. PMID: 16816025 Free PMC article.

9

Congenital encephalomyopathy with epilepsy, chorioretinitis, basal ganglia involvement, and muscle minicores.

Avoni P, Monari L, Carelli V, Carcangiu R, Barboni P, Donati C, Badiali L, Baruzzi A, Montagna P. Avoni P, et al. Among authors: montagna p. Ann Neurol. 2000 Mar;47(3):395-9. Ann Neurol. 2000. PMID: 10716265

10

A clinically complex form of dominant optic atrophy (OPA8) maps on chromosome 16.

Carelli V, Schimpf S, Fuhrmann N, Valentino ML, Zanna C, Iommarini L, Papke M, Schaich S, Tippmann S, Baumann B, Barboni P, Longanesi L, Rugolo M, Ghelli A, Alavi MV, Youle RJ, Bucchi L, Carroccia R, Giannoccaro MP, Tonon C, Lodi R, Cenacchi G, Montagna P, Liguori R, Wissinger B. Carelli V, et al. Among authors: montagna p. Hum Mol Genet. 2011 May 15;20(10):1893-905. doi: 10.1093/hmg/ddr071. Epub 2011 Feb 24. Hum Mol Genet. 2011. PMID: 21349918

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