ACNP - Italian Periodicals Catalogue

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Results: 1-23 |

Results: 23

Charcot-Marie-Tooth disease type I and related demyelinating neuropathies:Mutation analysis in a large cohort of Italian families

Authors: Mostacciuolo, ML Righetti, E Zortea, M Bosello, V Schiavon, F Vallo, L Merlini, L Siciliano, G Fabrizi, GM Rizzuto, N Milani, M Baratta, S Taroni, F

Citation: Ml. Mostacciuolo et al., Charcot-Marie-Tooth disease type I and related demyelinating neuropathies:Mutation analysis in a large cohort of Italian families, HUM MUTAT, 18(1), 2001, pp. 32-41

Respiratory chain defects in hereditary spastic paraplegias

Authors: Piemonte, F Casali, C Carrozzo, R Schagger, H Patrono, C Tessa, A Tozzi, G Cricchi, F Di Capua, M Siciliano, G Amabile, GA Morocutti, C Bertini, E Santorelli, FM

Citation: F. Piemonte et al., Respiratory chain defects in hereditary spastic paraplegias, NEUROMUSC D, 11(6-7), 2001, pp. 565-569

Coenzyme Q10, exercise lactate and CTG trinucleotide expansion in myotonicdystrophy

Authors: Siciliano, G Mancuso, M Tedeschi, D Manca, ML Renna, MR Lombardi, V Rocchi, A Martelli, F Murri, L

Citation: G. Siciliano et al., Coenzyme Q10, exercise lactate and CTG trinucleotide expansion in myotonicdystrophy, BRAIN RES B, 56(3-4), 2001, pp. 405-410

Limbic encephalitis associated with thymic cancer: a case report

Authors: D'Avino, C Lucchi, M Ceravolo, R Mussi, A Malandrini, A Annunziata, P Siciliano, G

Citation: C. D'Avino et al., Limbic encephalitis associated with thymic cancer: a case report, J NEUROL, 248(11), 2001, pp. 1000-1002

Low prevalence of TT virus in the cerebrospinal fluid of viremic patients with central nervous system disorders

Authors: Maggi, F Fornai, C Vatteroni, ML Siciliano, G Menichetti, F Tascini, C Specter, S Pistello, M Bendinelli, M

Citation: F. Maggi et al., Low prevalence of TT virus in the cerebrospinal fluid of viremic patients with central nervous system disorders, J MED VIROL, 65(2), 2001, pp. 418-422

Impaired oxidative metabolism in exercising muscle from ALS patients

Authors: Siciliano, G Pastorini, E Pasquali, L Manca, ML Iudice, A Murri, L

Citation: G. Siciliano et al., Impaired oxidative metabolism in exercising muscle from ALS patients, J NEUR SCI, 191(1-2), 2001, pp. 61-65

Mitochondrial DNA rearrangements in young onset parkinsonism: two case reports

Authors: Siciliano, G Mancuso, M Ceravolo, R Lombardi, V Iudice, A Bonuccelli, U

Citation: G. Siciliano et al., Mitochondrial DNA rearrangements in young onset parkinsonism: two case reports, J NE NE PSY, 71(5), 2001, pp. 685-687

Sudden bilateral hearing loss and sporadic mitochondrial DNA deletion

Authors: Berrettini, S Forli, F Siciliano, G Mancuso, M

Citation: S. Berrettini et al., Sudden bilateral hearing loss and sporadic mitochondrial DNA deletion, J LARYNG OT, 115(2), 2001, pp. 128-131

Epidemiology of myotonic dystrophy in Italy: re-apprisal after genetic diagnosis

Authors: Siciliano, G Manca, ML Gennarelli, M Angelini, C Rocchi, A Iudice, A Miorin, M Mostacciuolo, ML

Citation: G. Siciliano et al., Epidemiology of myotonic dystrophy in Italy: re-apprisal after genetic diagnosis, CLIN GENET, 59(5), 2001, pp. 344-349

Effects of grating spatial orientation on visual evoked potentials and contrast sensitivity in multiple sclerosis

Authors: Logi, F Pellegrinetti, A Bonfiglio, L Baglini, O Siciliano, G Iudice, A Sartucci, F

Citation: F. Logi et al., Effects of grating spatial orientation on visual evoked potentials and contrast sensitivity in multiple sclerosis, ACT NEUR SC, 103(2), 2001, pp. 97-104

Cytogenetic damage in peripheral lymphocytes of mitochondrial disease patients

Authors: Naccarati, A Molinu, S Mancuso, M Siciliano, G Migliore, L

Citation: A. Naccarati et al., Cytogenetic damage in peripheral lymphocytes of mitochondrial disease patients, NEUROL SCI, 21(5), 2000, pp. S963-S965

Potential involvement of ubiqninone in myotonic dystrophy pathophysiology:new diagnostic approaches for new rationale therapeutics

Authors: Tedeschi, D Lombardi, V Mancuso, M Martelli, F Sighieri, C Rocchi, A Tovani, S Siciliano, G Murri, L

Citation: D. Tedeschi et al., Potential involvement of ubiqninone in myotonic dystrophy pathophysiology:new diagnostic approaches for new rationale therapeutics, NEUROL SCI, 21(5), 2000, pp. S979-S980

Long-term treatment with idebenone and riboflavin in a patient with MELAS

Authors: Napolitano, A Salvetti, S Vista, M Lombardi, V Siciliano, G Giraldi, C

Citation: A. Napolitano et al., Long-term treatment with idebenone and riboflavin in a patient with MELAS, NEUROL SCI, 21(5), 2000, pp. S981-S982

Abnormal levels of human mitochondrial transcription factor A in skeletal muscle in mitochondrial encephalomyopathies

Authors: Siciliano, G Mancuso, M Pasquali, L Manca, ML Tessa, A Iudice, A

Citation: G. Siciliano et al., Abnormal levels of human mitochondrial transcription factor A in skeletal muscle in mitochondrial encephalomyopathies, NEUROL SCI, 21(5), 2000, pp. S985-S987

Phenotypic manifestations associated with CAG-repeat expansion in the androgen receptor gene in male patients and heterozygous females: a clinical and molecular study of 30 families

Authors: Mariotti, C Castellotti, B Pareyson, D Testa, D Eoli, M Antozzi, C Silani, V Marconi, R Tezzon, F Siciliano, G Marchini, C Gellera, C Di Donato, S

Citation: C. Mariotti et al., Phenotypic manifestations associated with CAG-repeat expansion in the androgen receptor gene in male patients and heterozygous females: a clinical and molecular study of 30 families, NEUROMUSC D, 10(6), 2000, pp. 391-397

Effects of aerobic training on lactate and catecholaminergic exercise responses in mitochondrial myopathies

Authors: Siciliano, G Manca, ML Renna, M Prontera, C Mercuri, A Murri, L

Citation: G. Siciliano et al., Effects of aerobic training on lactate and catecholaminergic exercise responses in mitochondrial myopathies, NEUROMUSC D, 10(1), 2000, pp. 40-45

Multiple mtDNA deletions: Clinical and molecular correlations

Authors: Santorelli, FM De Joanna, G Casali, C Tessa, A Siciliano, G Amabile, GA Pierelli, F Vilarinho, L Santoro, L

Citation: Fm. Santorelli et al., Multiple mtDNA deletions: Clinical and molecular correlations, J INH MET D, 23(2), 2000, pp. 155-161

Detection and quasispecies analysis of hepatitis C virus in the cerebrospinal fluid of infected patients

Authors: Maggi, F Giorgi, M Fornai, C Morrica, A Vatteroni, ML Pistello, M Siciliano, G Nuccorini, A Bendinelli, M

Citation: F. Maggi et al., Detection and quasispecies analysis of hepatitis C virus in the cerebrospinal fluid of infected patients, J NEUROVIRO, 5(3), 1999, pp. 319-323

Progressive sensorineural hearing loss in childhood

Authors: Berrettini, S Ravecca, F Sellari-Franceschini, S Matteucci, F Siciliano, G Ursino, F

Citation: S. Berrettini et al., Progressive sensorineural hearing loss in childhood, PED NEUROL, 20(2), 1999, pp. 130-136

Encephalomyopathy with multiple mitochondrial DNA deletions and multiple symmetric lipomatosis: further evidence of a possible association

Authors: Mancuso, M Bianchi, MC Santorelli, FM Tessa, A Casali, C Murri, L Siciliano, G

Citation: M. Mancuso et al., Encephalomyopathy with multiple mitochondrial DNA deletions and multiple symmetric lipomatosis: further evidence of a possible association, J NEUROL, 246(12), 1999, pp. 1197-1198

The clinical spectrum of sarcoglycanopathies

Authors: Angelini, C Fanin, M Freda, MP Duggan, DJ Siciliano, G Hoffman, EP

Citation: C. Angelini et al., The clinical spectrum of sarcoglycanopathies, NEUROLOGY, 52(1), 1999, pp. 176-179

Cortical silent period in patients with amyotrophic lateral sclerosis

Authors: Siciliano, G Manca, ML Sagliocco, L Pastorini, E Pellegrinetti, A Sartucci, F Sabatini, A Murri, L

Citation: G. Siciliano et al., Cortical silent period in patients with amyotrophic lateral sclerosis, J NEUR SCI, 169(1-2), 1999, pp. 93-97

Epidemiology of dystrophinopathies in North-West Tuscany: a molecular genetics-based revisitation

Authors: Siciliano, G Tessa, A Renna, M Manca, ML Mancuso, M Murri, L

Citation: G. Siciliano et al., Epidemiology of dystrophinopathies in North-West Tuscany: a molecular genetics-based revisitation, CLIN GENET, 56(1), 1999, pp. 51-58

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