The not trivial subdivision of nappes in the Lower Pennine domain of the Central Alps (Riviera and Verzasca Valleys, Swiss Alps)
2016-01-01 Schenker, Filippo Luca; Ambrosi, Christian; Scapozza, Cristian; Castelletti, Claudio; Maino, Matteo; Gouffon, Yves
The nappes of the Lepontine dome: the influence of tectonic inheritance on their deformation style
2017-01-01 Schenker, Fl; Ambrosi, C; Scapozza, C; Czerki, D; Castelletti, C; Maino, Matteo; Gouffon, Y.
Dating faults by quantifying shear heating
2017-01-01 Maino, Matteo; Casini, Leonardo; Langone, Antonio; Oggiano, Giacomo; Seno, Silvio; Stuart, Finlay
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.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| The not trivial subdivision of nappes in the Lower Pennine domain of the Central Alps (Riviera and Verzasca Valleys, Swiss Alps) | 1-gen-2016 | Schenker, Filippo Luca; Ambrosi, Christian; Scapozza, Cristian; Castelletti, Claudio; Maino, Matteo; Gouffon, Yves | |
| The nappes of the Lepontine dome: the influence of tectonic inheritance on their deformation style | 1-gen-2017 | Schenker, Fl; Ambrosi, C; Scapozza, C; Czerki, D; Castelletti, C; Maino, Matteo; Gouffon, Y. | |
| Dating faults by quantifying shear heating | 1-gen-2017 | Maino, Matteo; Casini, Leonardo; Langone, Antonio; Oggiano, Giacomo; Seno, Silvio; Stuart, Finlay | |
| 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. |
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Scopri
Tipologia
- 4 Contributo in Atti di Convegno ...3632
Data di pubblicazione
- In corso di stampa5
- 2020 - 2026315
- 2010 - 20191622
- 2000 - 20091045
- 1990 - 1999458
- 1980 - 1989179
- 1975 - 19798
Editore
- A.M.C.L.I.27
- Società Geologica Italiana20
- Centro Stampa Star snc17
- WILEY-BLACKWELL16
- AIChE(American Institute of Chemi...14
- Ente organizzatore del Congresso12
- Petruzzi Editore12
- Società Italiana di Igiene, Medic...11
- WILEY-LISS, DIV JOHN WILEY & SONS...11
- Ente organizzatore del congresso10
Rivista
- MICROBIOLOGIA MEDICA35
- CLINICAL MICROBIOLOGY AND INFECTION32
- HUMAN REPRODUCTION30
- EUROPEAN HEART JOURNAL27
- INTENSIVE CARE MEDICINE25
- MOVEMENT DISORDERS21
- EUROPEAN JOURNAL OF PUBLIC HEALTH17
- RENDICONTI ONLINE DELLA SOCIETÀ G...15
- EPITOME14
- MINERVA ANESTESIOLOGICA11
Serie
- CONFERENCE ON LASERS AND ELECTRO-...1
- EDULEARN PROCEEDINGS1
- PROCEEDINGS OF SPIE, THE INTERNAT...1
Keyword
- Hydrogen storage40
- Bioinformatics35
- Reactive hydride composites RHC35
- Synthetic Biology32
- Archeometria22
- Physico-chemical characterization21
- Southern Alps18
- Mg-based materials15
- archeometria14
- Hydrogen sorption14
Lingua
- eng2136
- ita719
- fre36
- spa7
- ger4
- rus2
- ukr2
- enm1
- hrv1
- tur1
Accesso al fulltext
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