Sfoglia per Autore
Dizzines: From clinical history to diagnostic hypothesis
2004 Bonavita, Vincenzo; DE SIMONE, Roberto
Towards the computerisation of ANIRCEF Headache Centres. Presentation of AIDA CEFALEE, a computer assisted diagnosis database for the management of headache patients
2004 DE SIMONE, Roberto; Marano, Enrico; Bonavita, Vincenzo
DEPRESSION IN NEUROLOGICAL DISEASES: A REVIEW.
2001 Bonavita, Vincenzo; Iavarone, A; Sorrentino, G.
Lack of sodium channel mutation in an Italian family with paramyotonia congenita
1999 Sampaolo, S; Puca, Md; Nigro, V; Cappa, V; Sannino, V; Sanges, G; Bonavita, Vincenzo; DI IORIO, G.
The Contursi kindred. A large family with autosomal dominant Parkinson's disease: implications of clinical and molecular studies.
1999 Golbe, L. I.; DI IORIO, G.; Lazzarini, A. M.; Vieregge, O. S.; Bonavita, Vincenzo
A comment on:"Molecular diagnosis of transthyretin Met30 mutation in an Italian family with familial amyloidotic polyneuropathy"
1996 Sanges, G; Sampaolo, S; Bonavita, Vincenzo; DI IORIO, G.
Clinical genetic analysis of parkinson's disease in the Contursi kindred.
1996 Golbe, L. I.; DI IORIO, G.; Sanges, G.; Lazzarini, A. M.; Bonavita, Vincenzo
A large kindred with Parkinson's disease: onset age, segregation ratios, anticipation.
1993 Golbe, L. I.; DI IORIO, G.; Lazzarini, A. M.; Bonavita, Vincenzo; Duvoisin, R. C.
A large kindred with autosomal dominant Parkinson's disease
1990 Golbe, L. I.; DI IORIO, G.; Bonavita, Vincenzo; Douglas, C.; Duvoisin, R. C.
| Titolo | Tipologia | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|---|
| Dizzines: From clinical history to diagnostic hypothesis | 1.1 Articolo in rivista | 2004 | Bonavita, Vincenzo; DE SIMONE, Roberto | |
| Towards the computerisation of ANIRCEF Headache Centres. Presentation of AIDA CEFALEE, a computer assisted diagnosis database for the management of headache patients | 1.1 Articolo in rivista | 2004 | DE SIMONE, Roberto; Marano, Enrico; Bonavita, Vincenzo | |
| DEPRESSION IN NEUROLOGICAL DISEASES: A REVIEW. | 1.1 Articolo in rivista | 2001 | Bonavita, Vincenzo; Iavarone, A; Sorrentino, G. | |
| Lack of sodium channel mutation in an Italian family with paramyotonia congenita | 1.1 Articolo in rivista | 1999 | Sampaolo, S; Puca, Md; Nigro, V; Cappa, V; Sannino, V; Sanges, G; Bonavita, Vincenzo; DI IORIO, G. | |
| The Contursi kindred. A large family with autosomal dominant Parkinson's disease: implications of clinical and molecular studies. | 1.1 Articolo in rivista | 1999 | Golbe, L. I.; DI IORIO, G.; Lazzarini, A. M.; Vieregge, O. S.; Bonavita, Vincenzo | |
| A comment on:"Molecular diagnosis of transthyretin Met30 mutation in an Italian family with familial amyloidotic polyneuropathy" | 1.1 Articolo in rivista | 1996 | Sanges, G; Sampaolo, S; Bonavita, Vincenzo; DI IORIO, G. | |
| Clinical genetic analysis of parkinson's disease in the Contursi kindred. | 1.1 Articolo in rivista | 1996 | Golbe, L. I.; DI IORIO, G.; Sanges, G.; Lazzarini, A. M.; Bonavita, Vincenzo | |
| A large kindred with Parkinson's disease: onset age, segregation ratios, anticipation. | 1.1 Articolo in rivista | 1993 | Golbe, L. I.; DI IORIO, G.; Lazzarini, A. M.; Bonavita, Vincenzo; Duvoisin, R. C. | |
| A large kindred with autosomal dominant Parkinson's disease | 1.1 Articolo in rivista | 1990 | Golbe, L. I.; DI IORIO, G.; Bonavita, Vincenzo; Douglas, C.; Duvoisin, R. C. |
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