Sfoglia per Rivista PARKINSONISM & RELATED DISORDERS
Association of nicotine dependence susceptibility gene, CHRNA5, with Parkinson's disease age at onset : gene and smoking status interaction
2013-01-01 Greenbaum, L.; Rigbi, A.; Lipshtat, N.; Cilia, R.; Tesei, S.; Asselta, R.; Djaldetti, R.; Goldwurm, S.; Lerer, B.
Glucocerebrosidase mutations in primary parkinsonism
2014-01-01 Asselta, R; Rimoldi, V; Siri, C; Cilia, R; Guella, I; Tesei, S; Solda', G; Pezzoli, G; Duga, S; Goldwurm, S
LRRK2 mutations in Parkinson's disease: confirmation of a gender effect in the Italian population
2014-01-01 Cilia, R; Siri, C; Rusconi, D; Allegra, R; Ghiglietti, A; Sacilotto, G; Zini, M; Zecchinelli, Al; Asselta, R; Duga, S; Paganoni, Am; Pezzoli, G; Seia, M; Goldwurm, S.
Neurofascin (NFASC) gene mutation causes autosomal recessive ataxia with demyelinating neuropathy.
2019-01-01 Monfrini, E; Straniero, L; Bonato, S; Monzio Compagnoni, G; Bordoni, A; Dilena, R; Rinchetti, P; Silipigni, R; Ronchi, D; Corti, S; Comi, Gp; Bresolin, N; Duga, S; Di Fonzo, A.
A rapid and low-cost test for screening the most common Parkinson's disease-related GBA variants
2020-01-01 Straniero, Letizia; Rimoldi, Valeria; Melistaccio, Giada; Di Fonzo, Alessio; Pezzoli, Gianni; Duga, Stefano; Asselta, Rosanna
SLC25A46 mutations in patients with Parkinson's Disease and optic atrophy
2020-01-01 Bitetto, Giacomo; Malaguti, Maria Chiara; Ceravolo, Roberto; Monfrini, Edoardo; Straniero, Letizia; Morini, Alberto; Di Giacopo, Raffaella; Frosini, Daniela; Palermo, Giovanni; Biella, Fabio; Ronchi, Dario; Duga, Stefano; Taroni, Franco; Corti, Stefania; Comi, Giacomo P; Bresolin, Nereo; Giometto, Bruno; Di Fonzo, Alessio
SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population
2012-01-01 Trotta, L; Guella, I; Soldà, G; Sironi, F; Tesei, S; Canesi, M; Pezzoli, G; Goldwurm, S; Duga, S; Asselta, R
Tryptophan Hydroxylase type 2 variants modulates severity and outcome of addictive behaviors in Parkinson's disease
2016-01-01 Cilia, R; Benfante, R; Asselta, R; Marabini, L; Cereda, E; Siri, C; Pezzoli, G; Goldwurm, S; Fornasari, D
Writer's cramp: Restoration of striatal D2-binding after successful biofeedback-based senorimotor training
2007-01-01 Berger, Hj; van der Werf, Sp; Horstink, Ca; Cools, Ar; Oyen, W; Horstink, Mw
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Association of nicotine dependence susceptibility gene, CHRNA5, with Parkinson's disease age at onset : gene and smoking status interaction | 1-gen-2013 | Greenbaum, L.; Rigbi, A.; Lipshtat, N.; Cilia, R.; Tesei, S.; Asselta, R.; Djaldetti, R.; Goldwurm, S.; Lerer, B. | |
| Glucocerebrosidase mutations in primary parkinsonism | 1-gen-2014 | Asselta, R; Rimoldi, V; Siri, C; Cilia, R; Guella, I; Tesei, S; Solda', G; Pezzoli, G; Duga, S; Goldwurm, S | |
| LRRK2 mutations in Parkinson's disease: confirmation of a gender effect in the Italian population | 1-gen-2014 | Cilia, R; Siri, C; Rusconi, D; Allegra, R; Ghiglietti, A; Sacilotto, G; Zini, M; Zecchinelli, Al; Asselta, R; Duga, S; Paganoni, Am; Pezzoli, G; Seia, M; Goldwurm, S. | |
| Neurofascin (NFASC) gene mutation causes autosomal recessive ataxia with demyelinating neuropathy. | 1-gen-2019 | Monfrini, E; Straniero, L; Bonato, S; Monzio Compagnoni, G; Bordoni, A; Dilena, R; Rinchetti, P; Silipigni, R; Ronchi, D; Corti, S; Comi, Gp; Bresolin, N; Duga, S; Di Fonzo, A. | |
| A rapid and low-cost test for screening the most common Parkinson's disease-related GBA variants | 1-gen-2020 | Straniero, Letizia; Rimoldi, Valeria; Melistaccio, Giada; Di Fonzo, Alessio; Pezzoli, Gianni; Duga, Stefano; Asselta, Rosanna | |
| SLC25A46 mutations in patients with Parkinson's Disease and optic atrophy | 1-gen-2020 | Bitetto, Giacomo; Malaguti, Maria Chiara; Ceravolo, Roberto; Monfrini, Edoardo; Straniero, Letizia; Morini, Alberto; Di Giacopo, Raffaella; Frosini, Daniela; Palermo, Giovanni; Biella, Fabio; Ronchi, Dario; Duga, Stefano; Taroni, Franco; Corti, Stefania; Comi, Giacomo P; Bresolin, Nereo; Giometto, Bruno; Di Fonzo, Alessio | |
| SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population | 1-gen-2012 | Trotta, L; Guella, I; Soldà, G; Sironi, F; Tesei, S; Canesi, M; Pezzoli, G; Goldwurm, S; Duga, S; Asselta, R | |
| Tryptophan Hydroxylase type 2 variants modulates severity and outcome of addictive behaviors in Parkinson's disease | 1-gen-2016 | Cilia, R; Benfante, R; Asselta, R; Marabini, L; Cereda, E; Siri, C; Pezzoli, G; Goldwurm, S; Fornasari, D | |
| Writer's cramp: Restoration of striatal D2-binding after successful biofeedback-based senorimotor training | 1-gen-2007 | Berger, Hj; van der Werf, Sp; Horstink, Ca; Cools, Ar; Oyen, W; Horstink, Mw |
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