Reverse fault growth and fault interaction with frictional interfaces: insights from analogue models
2017-01-01 Bonanno, Emanuele; Bonini, Lorenzo; Basili, R; Toscani, Giovanni; Seno, Silvio
Repeated saccades: The movement memory improves the accuracy of the memory guided saccades in humans
2007-01-01 Colnaghi, Silvia; Beltrami, Giorgio; Cosi, Vittorio; Versino, Maurizio
Silk fibroin nanoparticles dramatically reduce Celecoxib in vitro citotoxicity.
2017-01-01 Crivelli, Barbara; Perteghella, Sara; Catenacci, Laura; Sorrenti, MILENA LILLINA; Chlapanidas, Theodora; Torre, MARIA LUISA
PARK6 linked Parkinson's disease is caused by mutations in a mitochondrial protein kinase
2004-01-01 Valente, ENZA MARIA; Abou Sleiman, Pm; Caputo, V; Muqit, Mmk; Gispert, S; Ali, Z; Del Turco, D; Wingerter, O; Bentivoglio, Ar; Healy, Dg; Albanese, A; Nussbaum, R; Gonzalez Maldonado, R; Deller, T; Mulsch, A; Bratzke, H; Salvi, S; Cortelli, P; Gilks, Wp; Latchman, D; Harvey, R; Dallapiccola, B; Auburger, G; Wood, Nw
Clinical and molecular aspects of PINK1-related parkinsonism
2006-01-01 Silvestri, L; Caputo, V; Atorino, L; Dallapiccola, B; Valente, ENZA MARIA; Casari, G.
Genetic susceptibility in cervical dystonia: confirmation of a role for the dopamine D5 receptor gene
2002-01-01 Valente, ENZA MARIA; Brancati, F; Vanacore, N; Galardi, G; Berardelli, A; Dallapiccola, B.
RELATIONSHIP BETWEEN GENOTYPE AND ELECTROPHISIOLOGY ASSESSED BY ELECTRORETINOGRAM AND VISUAL EVOKED POTENTIALS IN 44 YOUNG PEOPLE AFFECTED BY JOUBERT SYNDROME
2015-01-01 Ruberto, Giulio; Signorini, Sabrina; Valente, ENZA MARIA; Antonini, Mauro; Ferro, Federica; Tinelli, Carmine; Bianchi, PAOLO EMILIO; Balottin, Umberto; Bertone, Chiara
Update on the genetics of dystonia
2003-01-01 Valente, ENZA MARIA
A novel genetic prediction score in myoclonus-dystonia
2012-01-01 Carecchio, M.; Magliozzi, M.; Copetti, M.; Ferraris, A.; Bernardini, L.; Bonetti, M.; Edwards, M. J.; Torrente, I.; Pellegrini, F.; Comi, C.; Bhatia, K. P.; Valente, ENZA MARIA
Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes
2010-01-01 Logan, Clare; Valente, ENZA MARIA; Zerelli, S. Mougou; Lee, J. H.; Silhavy, J. L.; Brancati, F.; Lannicelli, M.; Travaglini, L.; Romani, S.; Illi, B.; Adams, M.; Szymanska, K.; Lee, J. E.; Thomas, S.; Davis, E.; Vekemans, M.; Katsanis, N.; Bitach, T. Attie; Gleeson, J. G.; Johnson, C. A.
Partial caveolin 3 deficiency in acquired rippling muscle disease
2008-01-01 Mirabella, M.; Charlton, R.; Valente, ENZA MARIA; Petrini, S.; D'Amico, A.; Roberts, M.; Ricci, E.; De Benedetti, F.; Barresi, R.; Bertini, E.; Straub, V.
Advances in genetics of movement disorders
2008-01-01 Valente, ENZA MARIA
Defining the phenotypic signature of DYT11 mutations in myoclonus-dystonia patients
2010-01-01 Carecchio, M.; Bonetti, M.; Magliozzi, M.; Edwards, M. J.; Ferraris, A.; Torrente, I.; Valente, ENZA MARIA; Bhatia, K.
The syndrome of deafness-dystonia - A case series of 11 patients
2009-01-01 Kojovic, M.; Edwards, M. J.; Schneider, S.; Bitner, M.; Valente, ENZA MARIA; Bhatia, K. P.
Infantile neuroaxonal dystrophy in 14 Tunisian children
2012-01-01 Kraoua, I.; Romani, M.; Marouani, I.; Benrhouma, H.; Rouissi, A.; Turki, I.; Valente, ENZA MARIA; Gouider Khouja, N.
The Contursi family 20 years later: Intrafamilial variability in a kindred with A53T mutation of SCNA gene
2015-01-01 Ricciardi, L.; Petrucci, S.; Di Giuda, D.; Sensi, M. C.; Cocciolillo, F.; Ginevrino, Monia; Valente, ENZA MARIA; Fasano, A.
Cerebellar and brainstem congenital defects in Tunisian children
2012-01-01 Marouani, I.; Kraoua, I.; Benrhouma, H.; Rouissi, A.; Turki, I.; Valente, ENZA MARIA; Nagi, S.; Gouider Khouja, N.
Mild mitochondrial impairment promotes corticostriatal synaptic plasticity alterations in PINK1 heterozygous knockout mice
2016-01-01 Imbriani, P.; Martella, G.; Madeo, G.; Maltese, M.; Vanni, V.; Ferraro, E.; Valente, ENZA MARIA; Schirinzi, T.; Bonanni, L.; Shen, J.; Mercuri, N. B.; Bonsi, P.; Pisani, A.
Investigating the SGCE gene in myoclonic syndromes: Guidelines for diagnostic testing
2004-01-01 Edwards, Mj; Valente, ENZA MARIA; Mir, P; Di Giorgio, A; Salvi, S; Russo, N; Bozi, M; Pennisi, G; Dallapiccola, B; Bhatia, Kp
Brain-derived neurotrophic factor and risk for primary adult-onset cranial-cervical dystonia
2009-01-01 Martino, D.; Muglia, M.; Abbruzzese, G.; Berardelli, A.; Girlanda, P.; Macerollo, A.; Quattrone, A.; Roselli, F.; Sprovieri, T.; Valente, ENZA MARIA; Defazio, G.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Reverse fault growth and fault interaction with frictional interfaces: insights from analogue models | 1-gen-2017 | Bonanno, Emanuele; Bonini, Lorenzo; Basili, R; Toscani, Giovanni; Seno, Silvio | |
| Repeated saccades: The movement memory improves the accuracy of the memory guided saccades in humans | 1-gen-2007 | Colnaghi, Silvia; Beltrami, Giorgio; Cosi, Vittorio; Versino, Maurizio | |
| Silk fibroin nanoparticles dramatically reduce Celecoxib in vitro citotoxicity. | 1-gen-2017 | Crivelli, Barbara; Perteghella, Sara; Catenacci, Laura; Sorrenti, MILENA LILLINA; Chlapanidas, Theodora; Torre, MARIA LUISA | |
| PARK6 linked Parkinson's disease is caused by mutations in a mitochondrial protein kinase | 1-gen-2004 | Valente, ENZA MARIA; Abou Sleiman, Pm; Caputo, V; Muqit, Mmk; Gispert, S; Ali, Z; Del Turco, D; Wingerter, O; Bentivoglio, Ar; Healy, Dg; Albanese, A; Nussbaum, R; Gonzalez Maldonado, R; Deller, T; Mulsch, A; Bratzke, H; Salvi, S; Cortelli, P; Gilks, Wp; Latchman, D; Harvey, R; Dallapiccola, B; Auburger, G; Wood, Nw | |
| Clinical and molecular aspects of PINK1-related parkinsonism | 1-gen-2006 | Silvestri, L; Caputo, V; Atorino, L; Dallapiccola, B; Valente, ENZA MARIA; Casari, G. | |
| Genetic susceptibility in cervical dystonia: confirmation of a role for the dopamine D5 receptor gene | 1-gen-2002 | Valente, ENZA MARIA; Brancati, F; Vanacore, N; Galardi, G; Berardelli, A; Dallapiccola, B. | |
| RELATIONSHIP BETWEEN GENOTYPE AND ELECTROPHISIOLOGY ASSESSED BY ELECTRORETINOGRAM AND VISUAL EVOKED POTENTIALS IN 44 YOUNG PEOPLE AFFECTED BY JOUBERT SYNDROME | 1-gen-2015 | Ruberto, Giulio; Signorini, Sabrina; Valente, ENZA MARIA; Antonini, Mauro; Ferro, Federica; Tinelli, Carmine; Bianchi, PAOLO EMILIO; Balottin, Umberto; Bertone, Chiara | |
| Update on the genetics of dystonia | 1-gen-2003 | Valente, ENZA MARIA | |
| A novel genetic prediction score in myoclonus-dystonia | 1-gen-2012 | Carecchio, M.; Magliozzi, M.; Copetti, M.; Ferraris, A.; Bernardini, L.; Bonetti, M.; Edwards, M. J.; Torrente, I.; Pellegrini, F.; Comi, C.; Bhatia, K. P.; Valente, ENZA MARIA | |
| Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes | 1-gen-2010 | Logan, Clare; Valente, ENZA MARIA; Zerelli, S. Mougou; Lee, J. H.; Silhavy, J. L.; Brancati, F.; Lannicelli, M.; Travaglini, L.; Romani, S.; Illi, B.; Adams, M.; Szymanska, K.; Lee, J. E.; Thomas, S.; Davis, E.; Vekemans, M.; Katsanis, N.; Bitach, T. Attie; Gleeson, J. G.; Johnson, C. A. | |
| Partial caveolin 3 deficiency in acquired rippling muscle disease | 1-gen-2008 | Mirabella, M.; Charlton, R.; Valente, ENZA MARIA; Petrini, S.; D'Amico, A.; Roberts, M.; Ricci, E.; De Benedetti, F.; Barresi, R.; Bertini, E.; Straub, V. | |
| Advances in genetics of movement disorders | 1-gen-2008 | Valente, ENZA MARIA | |
| Defining the phenotypic signature of DYT11 mutations in myoclonus-dystonia patients | 1-gen-2010 | Carecchio, M.; Bonetti, M.; Magliozzi, M.; Edwards, M. J.; Ferraris, A.; Torrente, I.; Valente, ENZA MARIA; Bhatia, K. | |
| The syndrome of deafness-dystonia - A case series of 11 patients | 1-gen-2009 | Kojovic, M.; Edwards, M. J.; Schneider, S.; Bitner, M.; Valente, ENZA MARIA; Bhatia, K. P. | |
| Infantile neuroaxonal dystrophy in 14 Tunisian children | 1-gen-2012 | Kraoua, I.; Romani, M.; Marouani, I.; Benrhouma, H.; Rouissi, A.; Turki, I.; Valente, ENZA MARIA; Gouider Khouja, N. | |
| The Contursi family 20 years later: Intrafamilial variability in a kindred with A53T mutation of SCNA gene | 1-gen-2015 | Ricciardi, L.; Petrucci, S.; Di Giuda, D.; Sensi, M. C.; Cocciolillo, F.; Ginevrino, Monia; Valente, ENZA MARIA; Fasano, A. | |
| Cerebellar and brainstem congenital defects in Tunisian children | 1-gen-2012 | Marouani, I.; Kraoua, I.; Benrhouma, H.; Rouissi, A.; Turki, I.; Valente, ENZA MARIA; Nagi, S.; Gouider Khouja, N. | |
| Mild mitochondrial impairment promotes corticostriatal synaptic plasticity alterations in PINK1 heterozygous knockout mice | 1-gen-2016 | Imbriani, P.; Martella, G.; Madeo, G.; Maltese, M.; Vanni, V.; Ferraro, E.; Valente, ENZA MARIA; Schirinzi, T.; Bonanni, L.; Shen, J.; Mercuri, N. B.; Bonsi, P.; Pisani, A. | |
| Investigating the SGCE gene in myoclonic syndromes: Guidelines for diagnostic testing | 1-gen-2004 | Edwards, Mj; Valente, ENZA MARIA; Mir, P; Di Giorgio, A; Salvi, S; Russo, N; Bozi, M; Pennisi, G; Dallapiccola, B; Bhatia, Kp | |
| Brain-derived neurotrophic factor and risk for primary adult-onset cranial-cervical dystonia | 1-gen-2009 | Martino, D.; Muglia, M.; Abbruzzese, G.; Berardelli, A.; Girlanda, P.; Macerollo, A.; Quattrone, A.; Roselli, F.; Sprovieri, T.; Valente, ENZA MARIA; Defazio, G. |
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