Sfoglia per Autore LA MORGIA, CHIARA
Busulfan neurotoxicity and EEG abnormalities: a case report.
2004 LA MORGIA C; MONDINI S; GUARINO M; BONIFAZI F; CIRIGNOTTA F.
Effects of bilateral subthalamic deep brain stimulation (DBS) on orthostatic hypotension in Parkinson's disease: a case report.
2005 Antonelli F.; La Morgia C.; Pierangeli G.; Barletta G.; Antonini A.; Pezzoli A.; Cortelli P.
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.
Leber’s hereditary optuc neuropathy (LHON) “plus”: maternal clustering of extraocular features in two italian families.
2005 C. La Morgia; B. Mostacci; M. Stanzani; M. Amadori; C. Tonon; R. Lodi; R. Liguori; M.L. Valentino; P. Barboni; P. Montagna; V. Carelli
"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.
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.
Stati di male convulsivi ricorrenti nell'adulto: modalità di presentazione della encefalopatia di Hashimoto?
2006 ALESSANDRIA M.; RONDELLI F.; VEDOVELLO M.; LA MORGIA C.; RIGUZZI P.; RUBBOLI G.; VOLPI L.; TASSINARI CA.; MICHELUCCI R.
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.
Sleep Quality , school performances and driving habits in adolescents
2006 Cirignotta F; Mondini S; Baldi Antognini A; Cardini S; Contardi S; La Morgia C
Sleep Quality , school performances and driving habits in adolescents
2006 Cirignotta F; Mondini S; Baldi-Antognini A ; Nardini S; Contardi S; La Morgia C.
Leber's Hereditary Optic Neuropathy with childhood onset.
2006 Barboni P.; Savini G.; Valentino M.L.; La Morgia C.; Bellusci C.; De Negri A.M.; Sadun F.; Carta A.; Carbonelli M.; Sadun A.A.; 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.
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.
Grand rounds: could occupational exposure to n-hexane and other solvents precipitate visual failure in leber hereditary optic neuropathy?
2007 Valerio Carelli, Flavia Franceschini, Silvia Venturi, Piero Barboni, Giacomo Savini, Giuseppe Barbieri, Ettore Pirro, Chiara La Morgia, Maria L. Valentino, Francesca Zanardi, Francesco S. Violante, Stefano Mattioli
Rare mtDNA Variants in Leber's Hereditary Optic Neuropathy Families with Recurrence of Myoclonus
2007 C. La Morgia; A. Achilli; L. Iommarini; M. L. Valentino; P. Barboni; M. Pala; A. Olivieri; C. Tonon; R. Lodi; R. Vetrugno; B. Mostacci; R. Liguori; R. Carroccia; M. Amadori; P. Montagna; A. Torroni; V. Carelli
Augmentation of restless legs syndrome with long-term tramadol treatment.
2007 Vetrugno R.; La Morgia C.; D'Angelo R.; Loi D.; Provini F.; Plazzi G.; Montagna P.
Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background.
2007 Hudson G.; Carelli V.; Spruijt L.; Gerards M.; Mowbray C.; Achilli A.; Pyle A.; Elson J.; Howell N.; La Morgia C.; Valentino M.L.; Huoponen K.; Savontaus M.L.; Nikoskelainen E.; Sadun A.A.; Salomao S.R.; Belfort R. Jr; Griffiths P.; Man P.Y.; de Coo R.F.; Horvath R.; Zeviani M.; Smeets H.J.; Torroni A.; Chinnery P.F.
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.
OPA 1 mutations induce mitochondrial DNA instability and optic atrophy "plus" phenotypes
2008 Amati-Bonneau P.; Valentino M.L.; Reynier P.; Gallardo M.E.; Bornstein B.; Boissiere A.; Campos Y; Rivera H; de la Aleja J.G.; Carroccia R.; Iommarini L.; Labauge P.; Figarella-Branger D.; Marcorelles P.; Furby A.; Beauvais K.; Letournel F.; Liguori R.; La Morgia C.; Montagna P.; Liguori M.; Zanna C.; Rugolo M.; Cossarizza A.; Wissinger B.; Verny C.; Schwarzenbacher R.; Martin M.A.; Arenas J.; Ayuso C.; Garesse R.; Lenaers G.; Bonneau D.; Carelli V.
OPA1 mutations induce mitochondrial DNA instability and optic atrophy plus phenotypes
2008 Carelli, V; Reynier, P; Lucia, M; Labauge, P; Verny, C; Furby, A; Lenaers, G; Carroccia, R; Iommarini, L; La Morgia, C; Liguori, R; Zanna, C; Campos, Y; Arenas, J; Garesse, R; Wissinger, B; Bonneau, D; Amati-Bonneau, P
| Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
|---|---|---|---|---|---|---|
| Busulfan neurotoxicity and EEG abnormalities: a case report. | LA MORGIA C; MONDINI S; GUARINO M; BONIFAZI F; CIRIGNOTTA F. | 2004-01-01 | NEUROLOGICAL SCIENCES | - | 1.01 Articolo in rivista | - |
| Effects of bilateral subthalamic deep brain stimulation (DBS) on orthostatic hypotension in Parkinson's disease: a case report. | Antonelli F.; La Morgia C.; Pierangeli G.; Barletta G.; Antonini A.; Pezzoli A.; Cortelli P. | 2005-01-01 | CLINICAL AUTONOMIC RESEARCH | - | 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) | - |
| Leber’s hereditary optuc neuropathy (LHON) “plus”: maternal clustering of extraocular features in two italian families. | C. La Morgia; B. Mostacci; M. Stanzani; M. Amadori; C. Tonon; R. Lodi; R. Liguori; M.L. Valentino...; P. Barboni; P. Montagna; V. Carelli | 2005-01-01 | NEUROLOGICAL SCIENCES | - | 4.02 Riassunto (Abstract) | - |
| "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) | - |
| 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) | - |
| Stati di male convulsivi ricorrenti nell'adulto: modalità di presentazione della encefalopatia di Hashimoto? | ALESSANDRIA M.; RONDELLI F.; VEDOVELLO M.; LA MORGIA C.; RIGUZZI P.; RUBBOLI G.; VOLPI L.; TASSIN...ARI CA.; MICHELUCCI R. | 2006-01-01 | - | s.n | 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) | - |
| Sleep Quality , school performances and driving habits in adolescents | Cirignotta F; Mondini S; Baldi Antognini A; Cardini S; Contardi S; La Morgia C | 2006-01-01 | SLEEP | - | 1.06 Abstract in rivista | - |
| Sleep Quality , school performances and driving habits in adolescents | Cirignotta F; Mondini S; Baldi-Antognini A ; Nardini S; Contardi S; La Morgia C. | 2006-01-01 | SLEEP | - | 4.02 Riassunto (Abstract) | - |
| Leber's Hereditary Optic Neuropathy with childhood onset. | Barboni P.; Savini G.; Valentino M.L.; La Morgia C.; Bellusci C.; De Negri A.M.; Sadun F.; Carta ...A.; Carbonelli M.; Sadun A.A.; Carelli V. | 2006-01-01 | INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE | - | 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) | - |
| 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) | - |
| Grand rounds: could occupational exposure to n-hexane and other solvents precipitate visual failure in leber hereditary optic neuropathy? | Valerio Carelli, Flavia Franceschini, Silvia Venturi, Piero Barboni, Giacomo Savini, Giuseppe Bar...bieri, Ettore Pirro, Chiara La Morgia, Maria L. Valentino, Francesca Zanardi, Francesco S. Violante, Stefano Mattioli | 2007-01-01 | ENVIRONMENTAL HEALTH PERSPECTIVES | - | 1.01 Articolo in rivista | Grand Rounds.pdf |
| Rare mtDNA Variants in Leber's Hereditary Optic Neuropathy Families with Recurrence of Myoclonus | C. La Morgia; A. Achilli; L. Iommarini; M. L. Valentino; P. Barboni; M. Pala; A. Olivieri; C. Ton...on; R. Lodi; R. Vetrugno; B. Mostacci; R. Liguori; R. Carroccia; M. Amadori; P. Montagna; A. Torroni; V. Carelli | 2007-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |
| Augmentation of restless legs syndrome with long-term tramadol treatment. | Vetrugno R.; La Morgia C.; D'Angelo R.; Loi D.; Provini F.; Plazzi G.; Montagna P. | 2007-01-01 | MOVEMENT DISORDERS | - | 1.01 Articolo in rivista | - |
| Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background. | Hudson G.; Carelli V.; Spruijt L.; Gerards M.; Mowbray C.; Achilli A.; Pyle A.; Elson J.; Howell ...N.; La Morgia C.; Valentino M.L.; Huoponen K.; Savontaus M.L.; Nikoskelainen E.; Sadun A.A.; Salomao S.R.; Belfort R. Jr; Griffiths P.; Man P.Y.; de Coo R.F.; Horvath R.; Zeviani M.; Smeets H.J.; Torroni A.; Chinnery P.F. | 2007-01-01 | AMERICAN JOURNAL OF HUMAN GENETICS | - | 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 | - |
| OPA 1 mutations induce mitochondrial DNA instability and optic atrophy "plus" phenotypes | Amati-Bonneau P.; Valentino M.L.; Reynier P.; Gallardo M.E.; Bornstein B.; Boissiere A.; Campos Y...; Rivera H; de la Aleja J.G.; Carroccia R.; Iommarini L.; Labauge P.; Figarella-Branger D.; Marcorelles P.; Furby A.; Beauvais K.; Letournel F.; Liguori R.; La Morgia C.; Montagna P.; Liguori M.; Zanna C.; Rugolo M.; Cossarizza A.; Wissinger B.; Verny C.; Schwarzenbacher R.; Martin M.A.; Arenas J.; Ayuso C.; Garesse R.; Lenaers G.; Bonneau D.; Carelli V. | 2008-01-01 | BRAIN | - | 1.01 Articolo in rivista | - |
| OPA1 mutations induce mitochondrial DNA instability and optic atrophy plus phenotypes | Carelli, V; Reynier, P; Lucia, M; Labauge, P; Verny, C; Furby, A; Lenaers, G; Carroccia, R; Iomma...rini, L; La Morgia, C; Liguori, R; Zanna, C; Campos, Y; Arenas, J; Garesse, R; Wissinger, B; Bonneau, D; Amati-Bonneau, P | 2008-01-01 | NEUROLOGY | LIPPINCOTT WILLIAMS & WILKINS | 4.02 Riassunto (Abstract) | - |
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