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Results: 1-8 |
Results: 8
Functional evaluation of tubularized-incised plate repair of midshaft-proximal hypospadias using uroflowmetry
Authors: Marte, A Di Iorio, G De Pasquale, M Cotrufo, AM Di Meglio, D
Citation: A. Marte et al., Functional evaluation of tubularized-incised plate repair of midshaft-proximal hypospadias using uroflowmetry, BJU INT, 87(6), 2001, pp. 540-543
Biochemical analysis of cybrids expressing mitochondrial DNA from Contursikindred Parkinson's subjects
Authors: Swerdlow, RH Parks, JK Cassarino, DS Binder, DR Bennett, JP Di Iorio, G Golbe, LI Parker, WD
Citation: Rh. Swerdlow et al., Biochemical analysis of cybrids expressing mitochondrial DNA from Contursikindred Parkinson's subjects, EXP NEUROL, 169(2), 2001, pp. 479-485
Does abnormal neuronal excitability exist in myotonic dystrophy? I. Effects of the antiarrhythmic drug hydroquinidine on slow saccadic eye movements
Authors: Di Costanzo, A Mottola, A Toriello, A Di Iorio, G Tedeschi, G Bonavita, V
Citation: A. Di Costanzo et al., Does abnormal neuronal excitability exist in myotonic dystrophy? I. Effects of the antiarrhythmic drug hydroquinidine on slow saccadic eye movements, NEUROL SCI, 21(2), 2000, pp. 73-80
Does abnormal neuronal excitability exist in myotonic dystrophy? II. Effects of the antiarrhythmic drug hydroquinidine on apathy and hypersomnia
Authors: Di Costanzo, A Mottola, A Toriello, A Di Iorio, G Tedeschi, G Bonavita, V
Citation: A. Di Costanzo et al., Does abnormal neuronal excitability exist in myotonic dystrophy? II. Effects of the antiarrhythmic drug hydroquinidine on apathy and hypersomnia, NEUROL SCI, 21(2), 2000, pp. 81-86
A new de novo mutation of the connexin-32 gene in a patient with X-linked Charcot-Marie-Tooth type 1 disease
Authors: Di Iorio, G Cappa, V Ciccodicola, A Sampaolo, S Ammendola, A Sanges, G Giugliano, R D'Urso, M
Citation: G. Di Iorio et al., A new de novo mutation of the connexin-32 gene in a patient with X-linked Charcot-Marie-Tooth type 1 disease, NEUROL SCI, 21(2), 2000, pp. 109-112
Cognitive impairment in systemic lupus erythematosus: a follow-up study
Authors: Carlomagno, S Migliaresi, S Ambrosone, L Sannino, M Sanges, G Di Iorio, G
Citation: S. Carlomagno et al., Cognitive impairment in systemic lupus erythematosus: a follow-up study, J NEUROL, 247(4), 2000, pp. 273-279
Craniofacial pain followed by scalp necrosis and stroke. An unusual presentation of the primary antiphospholipid syndrome
Authors: Sanges, G Sampaolo, S Di Iorio, G
Citation: G. Sanges et al., Craniofacial pain followed by scalp necrosis and stroke. An unusual presentation of the primary antiphospholipid syndrome, J NEUROL, 246(2), 1999, pp. 134-135
Lack of sodium channel mutation in an Italian family with paramyotonia congenita
Authors: Sampaolo, S Puca, AA Nigro, V Cappa, V Sannino, V Sanges, G Bonavita, V Di Iorio, G
Citation: S. Sampaolo et al., Lack of sodium channel mutation in an Italian family with paramyotonia congenita, NEUROLOGY, 53(7), 1999, pp. 1549-1555
Risultati: 1-8 |