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Results: 1-17 |
Results: 17
Parenchymatous neurosyphilis
Authors: Lauria, G Erbetta, A Pareyson, D Sghirlanzoni, A
Citation: G. Lauria et al., Parenchymatous neurosyphilis, NEUROL SCI, 22(3), 2001, pp. 281-282
Epidermal nerve fiber density in sensory ganglionopathies: Clinical and neurophysiologic correlations
Authors: Lauria, G Sghirlanzoni, A Lombardi, R Pareyson, D
Citation: G. Lauria et al., Epidermal nerve fiber density in sensory ganglionopathies: Clinical and neurophysiologic correlations, MUSCLE NERV, 24(8), 2001, pp. 1034-1039
Spinal cord lesion due to epidural anesthesia
Authors: Lauria, G Chiapparini, L Pareyson, D Sghirlanzoni, A
Citation: G. Lauria et al., Spinal cord lesion due to epidural anesthesia, NEUROL SCI, 21(6), 2000, pp. 411-412
Chronic inflammatory demyelinating polyradiculoneuropathy: long-term course and treatment of 60 patients
Authors: Sghirlanzoni, A Solari, A Ciano, C Mariotti, C Fallica, E Pareyson, D
Citation: A. Sghirlanzoni et al., Chronic inflammatory demyelinating polyradiculoneuropathy: long-term course and treatment of 60 patients, NEUROL SCI, 21(1), 2000, pp. 31-37
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
Partial laminin alpha 2 chain deficiency in a patient with myopathy resembling inclusion body myositis
Authors: Di Blasi, C Mora, M Pareyson, D Farina, L Sghirlanzoni, A Vignier, N Blasevich, F Cornelio, F Guicheney, P Morandi, L
Citation: C. Di Blasi et al., Partial laminin alpha 2 chain deficiency in a patient with myopathy resembling inclusion body myositis, ANN NEUROL, 47(6), 2000, pp. 811-816
Clinical and magnetic resonance imaging findings in chronic sensory ganglionopathies
Authors: Lauria, G Pareyson, D Grisoli, M Sghirlanzoni, A
Citation: G. Lauria et al., Clinical and magnetic resonance imaging findings in chronic sensory ganglionopathies, ANN NEUROL, 47(1), 2000, pp. 104-109
Deletion of exons 11-17 and novel mutations of the galactocerebrosidase gene in adult- and early-onset patients with Krabbe disease
Authors: Selleri, S Torchiana, E Pareyson, D Lulli, L Bertagnolio, B Savoiardo, M Farina, L Carrara, F Filocamo, M Gatti, R Sghirlanzoni, A Uziel, G Finocchiaro, G
Citation: S. Selleri et al., Deletion of exons 11-17 and novel mutations of the galactocerebrosidase gene in adult- and early-onset patients with Krabbe disease, J NEUROL, 247(11), 2000, pp. 875-877
MR imaging and proton MR spectroscopy in adult Krabbe disease
Authors: Farina, L Bizzi, A Finocchiaro, G Pareyson, D Sghirlanzoni, A Bertagnolio, B",Savoiardo,"Naidu, S Singhal, BS Wenger, DA
Citation: L. Farina et al., MR imaging and proton MR spectroscopy in adult Krabbe disease, AM J NEUROR, 21(8), 2000, pp. 1478-1482
Imaging and outcome in severe complications of lumbar epidural anaesthesia: report of 16 cases
Authors: Chiapparini, L Sghirlanzoni, A Pareyson, D Savoiardo, M
Citation: L. Chiapparini et al., Imaging and outcome in severe complications of lumbar epidural anaesthesia: report of 16 cases, NEURORADIOL, 42(8), 2000, pp. 564-571
Cranial nerve involvement in CMT disease type 1 due to early growth response 2 gene mutation
Authors: Pareyson, D Taroni, F Botti, S Morbin, M Baratta, S Lauria, G Ciano, C Sghirlanzoni, A
Citation: D. Pareyson et al., Cranial nerve involvement in CMT disease type 1 due to early growth response 2 gene mutation, NEUROLOGY, 54(8), 2000, pp. 1696-1698
Relative frequencies of CAG expansions in spinocerebellar ataxia and dentatorubropallidoluysian atrophy in 116 Italian families
Authors: Filla, A Mariotti, C Caruso, G Coppola, G Cocozza, S Castaldo, I Calabrese, O Salvatore, E De Michele, G Riggio, MC Pareyson, D Gellera, C Di Donato, S
Citation: A. Filla et al., Relative frequencies of CAG expansions in spinocerebellar ataxia and dentatorubropallidoluysian atrophy in 116 Italian families, EUR NEUROL, 44(1), 2000, pp. 31-36
Chronic cryptogenic sensory polyneuropathy
Authors: Lauria, G Pareyson, D Sghirlanzoni, A
Citation: G. Lauria et al., Chronic cryptogenic sensory polyneuropathy, ARCH NEUROL, 57(5), 2000, pp. 759-760
Guidelines for the diagnosis of Charcot-Marie-Tooth disease and related neuropathies
Authors: Pareyson, D
Citation: D. Pareyson, Guidelines for the diagnosis of Charcot-Marie-Tooth disease and related neuropathies, ITAL J NEUR, 20(4), 1999, pp. 207-216
Clinical and molecular studies of 73 Italian families with autosomal dominant cerebellar ataxia type I: SCA1 and SCA2 are the most common genotypes
Authors: Pareyson, D Gellera, C Castellotti, B Antonelli, A Riggio, MC Mazzucchelli, F Girotti, F Pietrini, V Mariotti, C Di Donato, S
Citation: D. Pareyson et al., Clinical and molecular studies of 73 Italian families with autosomal dominant cerebellar ataxia type I: SCA1 and SCA2 are the most common genotypes, J NEUROL, 246(5), 1999, pp. 389-393
Charcot-Marie-Tooth disease type 2 and P0 gene mutations
Authors: Pareyson, D Sghirlanzoni, A Bolti, S Ciano, C Fallica, E Mora, M Taroni, F
Citation: D. Pareyson et al., Charcot-Marie-Tooth disease type 2 and P0 gene mutations, NEUROLOGY, 52(5), 1999, pp. 1110-1111
Activation of the contact system in cerebrospinal fluid of patients with Alzheimer disease
Authors: Bergamaschini, L Parnetti, L Pareyson, D Canziani, S Cugno, M Agostoni, A
Citation: L. Bergamaschini et al., Activation of the contact system in cerebrospinal fluid of patients with Alzheimer disease, ALZ DIS A D, 12(2), 1998, pp. 102-108
Risultati: 1-17 |