Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Laetitia C Schwab"'
Autor:
Maddalena Migliavacca, Maria Ester Bernardo, Michela Gabaldo, Elena Fratini, Maria Grazia Natali Sora, Francesco Morena, Jesus Segovia, Giada Farinelli, Alessandra Biffi, Gerald Downey, Clelia Di Serio, Federica Cugnata, Luigi Naldini, Cristina Baldoli, Sabata Martino, Francesca Tucci, Mirko Essing, Francesca Ferrua, Federica Barzaghi, Eugenio Montini, Stefano Scarparo, Andrea Calabria, Maria Pia Cicalese, Mara Sangalli, Paolo Silvani, Maddalena Fraschini, Alberto A. Zambon, Marina Sarzana, Laetitia C. Schwab, Alessandra G. Clerici, Sara Locatelli, Alessandro Aiuti, Salvatore Recupero, Stefano Zancan, Francesca Ciotti, Paola M.V. Rancoita, Fabiola De Mattia, Gigliola Antonioli, Maria Sessa, Massimo Filippi, Fabio Ciceri, Vera Gallo
Publikováno v:
Abstracts of the 46th Annual Meeting of the Society for Neuropediatrics.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f3c98d7c741137af7a7d58dd91889ba
https://doi.org/10.1055/s-0041-1739647
https://doi.org/10.1055/s-0041-1739647
Autor:
Federica Barzaghi, Francesco Morena, Maddalena Migliavacca, Jesus Segovia, Maria Ester Bernardo, Vera Gallo, Mara Sangalli, Marina Sarzana, Francesca Fumagalli, Laetitia C. Schwab, Maddalena Fraschini, Gerald Downey, Luigi Naldini, Elena Fratini, Francesca Ferrua, Maria Pia Cicalese, Sabata Martino, Francesca Tucci, Sara Locatelli, Alessandro Aiuti, Fabio Ciceri, Valeria Calbi, Francesca Ciotti, Fabiola De Mattia
Publikováno v:
Molecular Genetics and Metabolism. 132:S21-S22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6610d8814bcd31dd8a0d9788faa0bef
https://doi.org/10.1016/j.ymgme.2020.12.031
https://doi.org/10.1016/j.ymgme.2020.12.031
Publikováno v:
Neurobiology of Disease, Vol 102, Iss, Pp 105-112 (2017)
Huntington's disease (HD) is a genetic neurodegenerative disorder characterized by a triad of motor, psychiatric and cognitive deficits with the latter classically attributed to disruption of fronto-striatal circuits. However, emerging evidence sugge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c028a818b5fcd17f19b92db83300e0e
http://www.sciencedirect.com/science/article/pii/S0969996117300529
http://www.sciencedirect.com/science/article/pii/S0969996117300529
Autor:
Marina Sarzana, Massimo Filippi, Valeria Calbi, Vera Gallo, Francesca Fumagalli, Stefano Zancan, Jesus Segovia, Elena Fratini, Gigliola Antonioli, Maria Sessa, Sara Locatelli, Maria Grazia Natali Sora, Fabio Ciceri, Alessandro Aiuti, Alessandra Biffi, Maria Pia Cicalese, Marcella Facchini, Luigi Naldini, Alberto A. Zambon, Gerald Downey, Maria Ester Bernardo, Laetitia C. Schwab, Francesca Ciotti
Publikováno v:
Molecular Genetics and Metabolism. 132:S40
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33140e7aca530723b26b509ca3151812
https://doi.org/10.1016/j.ymgme.2020.12.081
https://doi.org/10.1016/j.ymgme.2020.12.081
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 87:975-981
Background Huntington9s disease (HD) is an autosomal dominant neurodegenerative disorder characterised by a triad of motor, psychiatric and cognitive deficits with the latter classically attributed to disruption of frontostriatal networks. However, e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8a3b5f3cd06f93f1d7a548fbec114b7
https://doi.org/10.1136/jnnp-2015-312413
https://doi.org/10.1136/jnnp-2015-312413
Autor:
Vera Gallo, Maria Ester Bernardo, Clelia De Serio, Paula M.V. Rancoita, Gerald Downey, Stefano Zancan, Serena Acquati, Francesca Tucci, John Sharpe, Francesca Fumagalli, Cristina Baldoli, Laetitia C. Schwab, Sabata Martino, Valeria Calbi, Luigi Naldini, Alessandro Aiuti, Fabiola De Mattia, Maria Grazia Natali Sora, Maria Sessa, Alessandra Biffi, Massimo Filippi, Fabio Ciceri, Alberto A. Zambon, Michela Gabaldo, Eugenio Montini
Publikováno v:
Molecular Genetics and Metabolism. 129:S59
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1084bfb180ff4ade95b475d019ce2e84
https://doi.org/10.1016/j.ymgme.2019.11.135
https://doi.org/10.1016/j.ymgme.2019.11.135
Autor:
Roger A. Barker, Janelle Drouin-Ouellet, Laetitia C Schwab, Sarah L Mason, Shaady N Garas, Shady N Garas, Simon R.W. Stott
Publikováno v:
Expert review of neurotherapeutics. 15(4)
Huntington's disease (HD) is an incurable, inherited, progressive neurodegenerative disorder that is defined by a combination of motor, cognitive and psychiatric features. Pre-clinical and clinical studies have demonstrated an important role for the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41af179c89ffaf1da3f227ccf7211975
https://pubmed.ncbi.nlm.nih.gov/26523752
https://pubmed.ncbi.nlm.nih.gov/26523752
Publikováno v:
Current Neuropharmacology
There has been a great deal of interest recently in genetic effects on neurocognitive performance in the healthy population. KIBRA -a postsynaptic protein from the WWC family of proteins- was identified in 2003 in the human brain and kidney and has r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98208a6e4098b53fe90cc9a66119e850
https://pubmed.ncbi.nlm.nih.gov/24851092
https://pubmed.ncbi.nlm.nih.gov/24851092
Autor:
Shaady N Garas, Janelle Drouin-Ouellet, Laetitia C Schwab, Stott, Roger A. Barker, Sarah L Mason
Publikováno v:
Expert Review of Neurotherapeutics. 15:1367-1367
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99f35a7a5f3832371aed529e0794d640
https://doi.org/10.1586/14737175.2015.1088179
https://doi.org/10.1586/14737175.2015.1088179
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 85:A70-A70
Background Huntington’s disease (HD) is an autosomal dominant condition which leads to progressive neurodegeneration and presents with a combination of motor, cognitive, affective and metabolic problems. Diagnosis of manifest HD currently relies so
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d95a43449c37ace0b8918038a6541c5a
https://doi.org/10.1136/jnnp-2014-309032.199
https://doi.org/10.1136/jnnp-2014-309032.199