Gabriella Silvestri
Gabriella Silvestri
Catholic University of Sacred Heart
Verified email at policlinicogemelli.it
Title
Cited by
Cited by
Year
MELAS: clinical features, biochemistry, and molecular genetics
E Ciafaloni, E Ricci, S Shanske, CT Moraes, G Silvestri, M Hirano, ...
Annals of Neurology: Official Journal of the American Neurological …, 1992
5481992
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorder
M Hirano, G Silvestri, DM Blake, A Lombes, C Minetti, E Bonilla, AP Hays, ...
Neurology 44 (4), 721-721, 1994
4471994
A new mtDNA mutation in the tRNA (Lys) gene associated with myoclonic epilepsy and ragged-red fibers (MERRF).
G Silvestri, CT Moraes, S Shanske, SJ Oh, S DiMauro
American journal of human genetics 51 (6), 1213, 1992
2771992
Atypical clinical presentations associated with the MELAS mutation at position 3243 of human mitochondrial DNA
CT Moraes, F Ciacci, G Silvestri, S Shanske, M Sciacco, M Hirano, ...
Neuromuscular Disorders 3 (1), 43-50, 1993
2741993
Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number of KpnI repeats at the 4q35 locus and clinical …
E Ricci, G Galluzzi, G Deidda, S Cacurri, L Colantoni, B Merico, N Piazzo, ...
Annals of Neurology: Official Journal of the American Neurological …, 1999
2391999
Clinical features associated with the A→ G transition at nucleotide 8344 of mtDNA (“MERRF mutation”)
G Silvestri, E Ciafaloni, FM Santorelli, S Shanske, S Servidei, WD Graf, ...
Neurology 43 (6), 1200-1200, 1993
2341993
Impaired sequence learning in carriers of the DYT1 dystonia mutation
MF Ghilardi, M Carbon, G Silvestri, V Dhawan, M Tagliati, S Bressman, ...
Annals of neurology 54 (1), 102-109, 2003
1982003
A new mtDNA mutation in the tRNALeu(UUR) gene associated with maternally inherited cardiomyopathy
G Silvestri, FM Santorelli, S Shanske, CB Whitley, LA Schimmenti, ...
Human mutation 3 (1), 37-43, 1994
1871994
Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progression
M Pescatori, A Broccolini, C Minetti, E Bertini, C Bruno, A D'amico, ...
The FASEB Journal 21 (4), 1210-1226, 2007
1812007
Coenzyme Q10 reverses pathological phenotype and reduces apoptosis in familial CoQ10 deficiency
S Di Giovanni, M Mirabella, A Spinazzola, P Crociani, G Silvestri, ...
Neurology 57 (3), 515-518, 2001
1782001
Characterization of the pattern of cognitive impairment in myotonic dystrophy type 1
A Modoni, G Silvestri, MG Pomponi, F Mangiola, PA Tonali, C Marra
Archives of Neurology 61 (12), 1943-1947, 2004
1672004
Dominantly inherited mitochondrial myopathy with multiple deletions of mitochondrial DNA: clinical, morphologic, and biochemical studies
S Servidei, M Zeviani, G Manfredi, E Ricci, G Silvestri, E Bertini, C Gellera, ...
Neurology 41 (7), 1053-1053, 1991
1671991
Apoptosis in mitochondrial encephalomyopathies with mitochondrial DNA mutations: a potential pathogenic mechanism
M Mirabella, S Di Giovanni, G Silvestri, P Tonali, S Servidei
Brain 123 (1), 93-104, 2000
1382000
Learning networks in health and Parkinson's disease: reproducibility and treatment effects
M Carbon, MF Ghilardi, A Feigin, M Fukuda, G Silvestri, MJ Mentis, ...
Human brain mapping 19 (3), 197-211, 2003
1242003
Cardiac features of Emery–Dreifuss muscular dystrophy caused by lamin A/C gene mutations
T Sanna, A Dello Russo, D Toniolo, M Vytopil, G Pelargonio, ...
European heart journal 24 (24), 2227-2236, 2003
1152003
Learning of a sequential motor skill comprises explicit and implicit components that consolidate differently
MF Ghilardi, C Moisello, G Silvestri, C Ghez, JW Krakauer
Journal of neurophysiology 101 (5), 2218-2229, 2009
1112009
Fatal infantile liver failure associated with mitochondrial DNA depletion
MRM Mazziotta, E Ricci, E Bertini, CD Vici, S Servidei, AB Burlina, ...
The Journal of pediatrics 121 (6), 896-901, 1992
1101992
Widespread tissue distribution of a tRNALeu (UUR) mutation in the mitochondrial DNA of a patient with MELAS syndrome
E Ciafaloni, E Ricci, S Servidei, S Shanske, G Silvestri, G Manfredi, ...
Neurology 41 (10), 1663-1663, 1991
1101991
Nocturnal sleep and daytime somnolence in untreated patients with temporal lobe epilepsy: changes after treatment with controlled‐release carbamazepine
GL Gigli, F Placidi, M Diomedi, M Maschio, G Silvestri, A Scalise, ...
Epilepsia 38 (6), 696-701, 1997
1041997
The differential effect of PD and normal aging on early explicit sequence learning
MF Ghilardi, D Eidelberg, G Silvestri, C Ghez
Neurology 60 (8), 1313-1319, 2003
942003
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