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- Virgintino, D
- Roncali, L
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- Brizzi, T
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- Toscano, A
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In:
European journal of neurology vol. 26
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Cerebellar ataxia and severe muscle CoQ10 deficiency in a patient with a novel mutation in ADCK3. [electronic resource] by
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- Musumeci, O
- Montagnese, F
- Marino, S
- Granata, F
- Nunnari, D
- Peverelli, L
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- Quinzii, C M
- Toscano, A
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In:
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Effect of ACTH4-10 on nerve fiber regeneration after sciatic nerve crush in rabbits: an electrophysiological and morphological study. [electronic resource] by
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- Vita, G
- Dattola, R
- Santoro, M
- Toscano, A
- Venuto, C
- Roberto, M L
- Baradello, A
- Romano, M
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In:
Experimental neurology vol. 99
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Early-onset cerebellar ataxia, myoclonus and hypogonadism in a case of mitochondrial complex III deficiency treated with vitamins K3 and C. [electronic resource] by
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- Vita, G
- Cannavó, S
- Bresolin, N
- Bet, L
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- Iotti, S
- Zaniol, P
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In:
Journal of neurology vol. 242
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Duplication of dystrophin gene and dissimilar clinical phenotype in the same family. [electronic resource] by
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- Vitiello, L
- Comi, G P
- Galvagni, F
- Miorin, M
- Prelle, A
- Fortunato, F
- Bardoni, A
- Mora, M
- Fiumara, A
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Complete transposition of the great arteries: patterns of congenital heart disease in familial precurrence. [electronic resource] by
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- Casey, B
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- Pacileo, G
- Marasini, M
- Banaudi, E
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- Dallapiccola, B
- Marino, B
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In:
Circulation vol. 104
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Spectrum of atrial septal defects associated with mutations of NKX2.5 and GATA4 transcription factors. [electronic resource] by
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- Conti, E
- Neri, C
- D'Agostino, R
- Digilio, M C
- Esposito, G
- Toscano, A
- Marino, B
- Pizzuti, A
- Dallapiccola, B
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In:
Journal of medical genetics vol. 42
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Prevalence survey of major neurological disorders in Sicily. Results of a pilot study. [electronic resource] by
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- Morgante, L
- Grigoletto, F
- Santoro, M
- Toscano, A
- Coraci, M A
- Meneghini, F
- Venuto, C
- Fazio, C
- Troilo, G
Producer: 19891114
In:
Journal of neurology vol. 236
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118.
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Clinical and molecular aspects of 30 patients with late-onset Pompe disease (LOPD): unusual features and response to treatment. [electronic resource] by
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- Barca, E
- Musumeci, O
- Mondello, S
- Migliorato, A
- Ciranni, A
- Rodolico, C
- De Filippi, P
- Danesino, C
- Toscano, A
Producer: 20160108
In:
Journal of neurology vol. 262
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Identification of a new polymorphism (c134G>A) in the exon 2 of the myelin protein zero gene. [electronic resource] by
- Muglia, M
- Toscano, A
- Gabriele, A L
- Magariello, A
- Patitucci, A
- Conforti, F L
- Mazzei, R
- Rodolico, C
- Gambardella, A
- Quattrone, A
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In:
Human mutation vol. 15
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120.
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Clinical and muscle magnetic resonance imaging study of an Italian family with autosomal dominant inclusion body myopathy not linked to known genetic loci. [electronic resource] by
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- Toscano, A
- Patitucci, A
- Muglia, M
- Gaeta, M
- D'Arrigo, G
- Migliorato, A
- Messina, S
- Quattrone, A
- Messina, C
- Vita, G
Producer: 20060302
In:
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology vol. 26
Availability: No items available.
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