Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Stéphanie de Bournonville"'
Autor:
Jérôme Ausseil, Béatrice Poirier-Beaudouin, Marie-Lise Gougeon, Béatrice Husson, Dimitrios I. Zafeiriou, Marc Tardieu, Giancarlo Parenti, Kumaran Deiva, Michel Zerah, Stéphanie de Bournonville, Jean-Michel Heard
Publikováno v:
Human Gene Therapy
Human Gene Therapy, 2021, 32 (19-20), pp.1251-1259. ⟨10.1089/hum.2021.135⟩
Human Gene Therapy, 2021, 32 (19-20), pp.1251-1259. ⟨10.1089/hum.2021.135⟩
International audience; We report the safety (primary endpoint) and efficacy (secondary endpoint) of a novel intracerebral gene therapy at 5.5 years of follow-up in children with Sanfilippo B. An uncontrolled, phase 1/2 clinical trial was performed i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5656e00806ab496dfb15526727215b31
http://hdl.handle.net/11588/870281
http://hdl.handle.net/11588/870281
Autor:
Jérôme Ausseil, Béatrice Husson, Dimitrios I. Zafeiriou, Kumaran Deiva, Valérie Furlan, Béatrice Poirier, Christian Meyer, Philippe Bourget, Stéphanie de Bournonville, Cecile Artaud, Marc Tardieu, Thomas Roujeau, Jean-Michel Heard, Giancarlo Parenti, Thomas Baugnon, Marie-Lise Gougeon, M. Zerah, Ronald G. Crystal
Publikováno v:
The Lancet. Neurology. 16(9)
Summary Background Mucopolysaccharidosis type IIIB syndrome (also known as Sanfilippo type B syndrome) is a lysosomal storage disease resulting in progressive deterioration of cognitive acquisition after age 2–4 years. No treatment is available for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cabf2f6cd273dbf43781ae1c7db93732
https://pubmed.ncbi.nlm.nih.gov/28752858
https://pubmed.ncbi.nlm.nih.gov/28752858
Autor:
Andrea Ballabio, Michel Zerah, Michaël Hocquemiller, Valérie Furlan, Ronald G. Crystal, Fanny Vincent, Thomas Roujeau, Marc Tardieu, Thomas Baugnon, Jean-Michel Heard, Alessandro Fraldi, Kumaran Deiva, Stéphanie de Bournonville, Olivier Danos, Christine Broissand, Catherine Adamsbaum, Béatrice Husson
Publikováno v:
Human Gene Therapy. 25:506-516
Mucopolysaccharidosis type IIIA is a severe degenerative disease caused by an autosomal recessive defect of a gene encoding a lysosomal heparan-N-sulfamidase, the N-sulfoglycosamine sulfohydrolase (SGSH), the catalytic site of which is activated by a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5ff1bf774e4bf3fc01cb3b1a3fff313
https://doi.org/10.1089/hum.2013.238
https://doi.org/10.1089/hum.2013.238
Autor:
Bernard Dan, Xavier Noël, Céline Baurain, Martial Van der Linden, Stéphanie de Bournonville, Joël Billieux, Paul Verbanck, Catherine Hanak
Publikováno v:
Journal of Clinical and Experimental Neuropsychology, Vol. 31, No 1 (2009) pp. 57-64
Cognitive impairment has been associated with higher risk of alcoholism and relapse. Recent theoretical refinements have separated inhibition of dominant response and inhibition of proactive interference. We assessed the latter using a directed-forge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::628a932b733664a91d71f763450c7d92
https://doi.org/10.1080/13803390801982726
https://doi.org/10.1080/13803390801982726
Autor:
Giancarlo Parenti, Stéphanie de Bournonville, Cecile Artaud, Ronald G. Crystal, Kumaran Deiva, Thomas Roujeau, Dimitrios I. Zafeiriou, Jérôme Ausseil, Noami VanVlies, Marc Tardieu, Thomas Baugnon, Jean-Michel Heard, Philippe Bourget, M. Zerah, Marie-Lise Gougeon, Charles W. Richard, Béatrice Husson, Béatrice Poirier
Publikováno v:
Molecular Genetics and Metabolism. 120:S130
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::42633f98fe3c7250a67d9d063860c594
https://doi.org/10.1016/j.ymgme.2016.11.341
https://doi.org/10.1016/j.ymgme.2016.11.341