BELLAN, MARZIO
BELLAN, MARZIO
DIP. DI SCIENZE NEUROLOGICHE
"Plus" features of Leber's Hereditary Optic Neuropathy in nineteen Italian families.
2006 La Morgia C.; Valentino M.L.; Barboni P.; Bellan M.; Carroccia R.; Liguori R.; Avoni P.; Cortelli P.; Montagna P.; Baruzzi A.; Carelli V.
A new case of Sando syndrome and retinitis pigmentosa with novel combination of compound heterozygous POLG mutations.
2006 Bellan M.; Avoni P.; Liguori R.; Carroccia R.; Valentino M.L.; Villanova M.; La Morgia C.; Fulitano D.; Baruzzi A.; Lodi R.; Tonon C.; Lamantea E.; Zeviani M.; Carelli V.
Extraocular Clinical Features in Leber's Hereditary Optic Neuropathy (LHON) Italian Families.
2006 La Morgia C.; Valentino M.L.; Barboni P.; Bellan M.; Carroccia R.; Liguori R.; Avoni P.; Cortelli P.; Montagna P.; Baruzzi A.; Carelli V.
Extreme variability in genotype/phenotype correlation in an Italian family carrying the mtDNA A3243G/tRNALeu(UUR) MELAS mutation.
2005 Amadori M.; Liguori R.; Cantalupo G.; Rizzo G.; La Morgia C.; Avoni P.; Fortuna F.; Bellan M.; Carroccia R.; Montagna P.; Baruzzi A.; Carelli V.
Mitochondrial neurogastrointestinal encephalomyopathy: evidence of mitochondrial DNA depletion in the small intestine.
2006 Giordano C.; Sebastiani M.; Plazzi G.; Travaglini C.; Sale P.; Pinti M.; Tancredi A.; Liguori R.; Montagna P.; Bellan M.; Valentino M.L.; Cossarizza A.; Hirano M.; d'Amati G.; Carelli V.
Mitochondrial optic neuropathies: how two genomes may kill the same cell type?
2007 Carelli V.; La Morgia C.; Iommarini L.; Carroccia R.; Mattiazzi M.; Sangiorgi S.; Farné S.; Maresca A.; Foscarini B.; Lanzi L.; Amadori M.; Bellan M.; Valentino M.L.
Myelin, mitochondria, and autoimmunity: what's the connection?
2008 Carelli V.; Bellan M.
Myopathy and retinopathy are novel features in a patient with Mohr-Tranebjaerg syndrome.
2006 Bellan M.; La Morgia C.; Liguori R.; Villanova M.; Carroccia R.; Avoni P.; Lodi R.; Tonon C.; Baruzzi A.; Carelli V.
Ocular findings in mitochondrial neurogastrointestinal encephalomyopathy: a case report.
2004 BARBONI P; SAVINI G; PLAZZI G.; BELLAN M; VALENTINO ML; ZANINI M; MONTAGNA P; HIRANO M; CARELLI V.
OPA1 Gene Screening in Italian Dominant Optic Neuropathy (DOA) Patients Reveals New Mutations and Genetic Heterogeneity.
2006 Carelli V.; Schimpf S.; Valentino M.L.; Barboni P.; De Negri A.M.; Sadun F.; La Morgia C.; Bellan M.; Amadori M.; Schaich S.; Wissinger B.
POLG mutations causing ophthalmoplegia, sensorimotor polyneuropathy, ataxia, and deafness.
2004 MANCUSO M; FILOSTO M; BELLAN M; LIGUORI R; MONTAGNA P; BARUZZI A.; DIMAURO S; CARELLI V.
Polyneuropathy in patients with mitochondrial disorders: clinical, electrophysiological and genetic evaluations.
2006 Di Stasi V.; Avoni P.; Carelli V.; Donadio V.; Valentino L.; Bellan M.; Baruzzi A.; Montagna P.; Liguori R.
| Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
|---|---|---|---|---|---|---|
| "Plus" features of Leber's Hereditary Optic Neuropathy in nineteen Italian families. | La Morgia C.; Valentino M.L.; Barboni P.; Bellan M.; Carroccia R.; Liguori R.; Avoni P.; Cortelli... P.; Montagna P.; Baruzzi A.; Carelli V. | 2006-01-01 | NEUROLOGICAL SCIENCES | - | 4.02 Riassunto (Abstract) | - |
| A new case of Sando syndrome and retinitis pigmentosa with novel combination of compound heterozygous POLG mutations. | Bellan M.; Avoni P.; Liguori R.; Carroccia R.; Valentino M.L.; Villanova M.; La Morgia C.; Fulita...no D.; Baruzzi A.; Lodi R.; Tonon C.; Lamantea E.; Zeviani M.; Carelli V. | 2006-01-01 | NEUROLOGICAL SCIENCES | - | 4.02 Riassunto (Abstract) | - |
| Extraocular Clinical Features in Leber's Hereditary Optic Neuropathy (LHON) Italian Families. | La Morgia C.; Valentino M.L.; Barboni P.; Bellan M.; Carroccia R.; Liguori R.; Avoni P.; Cortelli... P.; Montagna P.; Baruzzi A.; Carelli V. | 2006-01-01 | NEUROLOGY | - | 4.02 Riassunto (Abstract) | - |
| Extreme variability in genotype/phenotype correlation in an Italian family carrying the mtDNA A3243G/tRNALeu(UUR) MELAS mutation. | Amadori M.; Liguori R.; Cantalupo G.; Rizzo G.; La Morgia C.; Avoni P.; Fortuna F.; Bellan M.; Ca...rroccia R.; Montagna P.; Baruzzi A.; Carelli V. | 2005-01-01 | NEUROLOGICAL SCIENCES | - | 4.02 Riassunto (Abstract) | - |
| 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 M.L.; Cossarizza A.; Hirano M.; d'Amati G.; Carelli V. | 2006-01-01 | GASTROENTEROLOGY | - | 1.01 Articolo in rivista | - |
| Mitochondrial optic neuropathies: how two genomes may kill the same cell type? | Carelli V.; La Morgia C.; Iommarini L.; Carroccia R.; Mattiazzi M.; Sangiorgi S.; Farné S.; Mares...ca A.; Foscarini B.; Lanzi L.; Amadori M.; Bellan M.; Valentino M.L. | 2007-01-01 | BIOSCIENCE REPORTS | - | 1.01 Articolo in rivista | - |
| Myelin, mitochondria, and autoimmunity: what's the connection? | Carelli V.; Bellan M. | 2008-01-01 | NEUROLOGY | - | 1.04 Replica / breve intervento (e simili) | - |
| Myopathy and retinopathy are novel features in a patient with Mohr-Tranebjaerg syndrome. | Bellan M.; La Morgia C.; Liguori R.; Villanova M.; Carroccia R.; Avoni P.; Lodi R.; Tonon C.; Bar...uzzi A.; Carelli V. | 2006-01-01 | NEUROLOGICAL SCIENCES | - | 4.02 Riassunto (Abstract) | - |
| 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. | 2004-01-01 | GRAEFE'S ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY | - | 1.01 Articolo in rivista | - |
| OPA1 Gene Screening in Italian Dominant Optic Neuropathy (DOA) Patients Reveals New Mutations and Genetic Heterogeneity. | Carelli V.; Schimpf S.; Valentino M.L.; Barboni P.; De Negri A.M.; Sadun F.; La Morgia C.; Bellan... M.; Amadori M.; Schaich S.; Wissinger B. | 2006-01-01 | NEUROLOGY | - | 4.02 Riassunto (Abstract) | - |
| POLG mutations causing ophthalmoplegia, sensorimotor polyneuropathy, ataxia, and deafness. | MANCUSO M; FILOSTO M; BELLAN M; LIGUORI R; MONTAGNA P; BARUZZI A.; DIMAURO S; CARELLI V. | 2004-01-01 | NEUROLOGY | - | 1.01 Articolo in rivista | - |
| Polyneuropathy in patients with mitochondrial disorders: clinical, electrophysiological and genetic evaluations. | Di Stasi V.; Avoni P.; Carelli V.; Donadio V.; Valentino L.; Bellan M.; Baruzzi A.; Montagna P.; ...Liguori R. | 2006-01-01 | NEUROLOGICAL SCIENCES | - | 4.02 Riassunto (Abstract) | - |