Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Juliette, Ropars"'
Autor:
Théau Cavillon, Elise Sacaze, Jean Baptiste Noury, Claire Abasq, Gaelle Cornen, Juliette Ropars, Valérie Devauchelle-Pensec
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 22, Iss 1, Pp 1-3 (2024)
Externí odkaz:
https://doaj.org/article/8e0280a8a9b44843b8ad0cd000238623
Autor:
Isabelle Desguerre, Rémi Barrois, Frédérique Audic, Christine Barnerias, Brigitte Chabrol, Jean Baptiste Davion, Julien Durigneux, Caroline Espil-Taris, Marta Gomez-Garcia de la Banda, Marine Guichard, Arnaud Isapof, Marie Christine Nougues, Vincent Laugel, Laure Le Goff, Sandra Mercier, Anne Pervillé, Christian Richelme, Marie Thibaud, Catherine Sarret, Cyril Schweitzer, Hervé Testard, Valérie Trommsdorff, Catherine Vanhulle, Ulrike Walther-Louvier, Cécilia Altuzarra, Mondher Chouchane, Juliette Ropars, Susana Quijano-Roy, Claude Cances
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-11 (2024)
Abstract Background Spinal muscular atrophy type 1 (SMA1) is the most severe and early form of SMA, a genetic disease with motor neuron degeneration. Onasemnogene abeparvovec gene transfer therapy (GT) has changed the natural history of SMA1, but rea
Externí odkaz:
https://doaj.org/article/15c4bb3f54a24e75bc25f097944bb5f3
Autor:
Yann T. Le Guen, Chantal Pichon, Philippe Guégan, Kévin Pluchon, Tanguy Haute, Sandrine Quemener, Juliette Ropars, Patrick Midoux, Tony Le Gall, Tristan Montier
Publikováno v:
Molecular Therapy: Nucleic Acids, Vol 24, Iss , Pp 477-486 (2021)
An important bottleneck for non-viral gene transfer commonly relates to translocation of nucleic acids into the nuclear compartment of target cells. So-called 3NFs are optimized short nucleotide sequences able to interact with the transcription facto
Externí odkaz:
https://doaj.org/article/cbbf416e03b24cf5ad0af59a2047b63f
Autor:
Frédérique Audic, Marta Gomez Garcia de la Banda, Delphine Bernoux, Paola Ramirez-Garcia, Julien Durigneux, Christine Barnerias, Arnaud Isapof, Jean-Marie Cuisset, Claude Cances, Christian Richelme, Carole Vuillerot, Vincent Laugel, Juliette Ropars, Cécilia Altuzarra, Caroline Espil-Taris, Ulrike Walther-Louvier, Pascal Sabouraud, Mondher Chouchane, Catherine Vanhulle, Valérie Trommsdorff, Anne Pervillé, Hervé Testard, Emmanuelle Lagrue, Catherine Sarret, Anne-Laude Avice, Pierre Beze-Beyrie, Vanessa Pauly, Susana Quijano-Roy, Brigitte Chabrol, Isabelle Desguerre
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-10 (2020)
Abstract Background Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disorder characterized by degeneration of the anterior horn cells of the spinal cord. Nusinersen has been covered by public healthcare in France since May 2017.
Externí odkaz:
https://doaj.org/article/318647e3ed8f4622944ee433cb371756
Publikováno v:
Pediatric Neurology. 142:76-88
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91444b7d752818c14a48c62623bcfd63
https://doi.org/10.1016/j.pediatrneurol.2023.01.005
https://doi.org/10.1016/j.pediatrneurol.2023.01.005
Autor:
Juliette, Ropars, Elise, Sacaze, Lydie, Abalea, Sylviane, Peudenier, Philippe, Vic, Laurence, Lemoigno, Thomas, Dailland, Lisa, Courgeon, Jeremie, Lefranc
Publikováno v:
Neuropediatrics. 53:440-444
Objective This study was aimed to determine the rate, timing, and risk factors of acute recurrence of seizures in the children admitted for nonfebrile seizure in the emergency department (ED). Methods This multicenter prospective study was conducted
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20f826e2d35ad0ad21af2163749a0022
https://doi.org/10.1055/a-1889-8388
https://doi.org/10.1055/a-1889-8388
Autor:
Nathan Decaux, Pierre-Henri Conze, Juliette Ropars, Xinyan He, Frances T. Sheehan, Christelle Pons, Douraied Ben Salem, Sylvain Brochard, François Rousseau
Publikováno v:
Pattern Recognition. 140:109529
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7736e9ca55887772447f8f0f48672f3a
https://doi.org/10.1016/j.patcog.2023.109529
https://doi.org/10.1016/j.patcog.2023.109529
Publikováno v:
Les Cahiers de Myologie. :12-17
Les nombreux travaux précliniques de thérapie génique (TG) mis en œuvre afin de modifier l’histoire naturelle de la dystrophie musculaire de Duchenne (DMD), ont aujourd’hui abouti à la mise en place d’essais cliniques évaluant la sécurit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1cd1629756eb20bca4cd7f49ee4e8de4
https://doi.org/10.1051/myolog/202123004
https://doi.org/10.1051/myolog/202123004
Autor:
Johanne Mensah-Gourmel, Maxime Bourgain, Christèle Kandalaft, Alain Chatelin, Odile Tissier, Guy Letellier, Jan Willem Gorter, Sylvain Brochard, Christelle Pons, Asma Benyahia, Inès Bréchoire, Pauline Julia, Tuong-Xuân Nguyen-Luong, Pierre Mirlesse, Tomas Studenik, Sebastien Loriot, Brian Tesar, Nolwenn Le Menn, Thomas Gayon, Amelie Genot, Juliette Ropars, Christopher J Newman, Julie Paradis, Laetitia Houx, Rodolphe Bailly, Martine Venineaux
Publikováno v:
Disability and rehabilitation. Assistive technology.
Technical solutions could facilitate activities and participation in individuals with disabilities. For the development of solutions, hackathons are a method of interdisciplinary collaboration. For hackathon, the definition of pain points that requir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dab35a077e1d7c432d7b4235fde131db
https://pubmed.ncbi.nlm.nih.gov/36036377
https://pubmed.ncbi.nlm.nih.gov/36036377
Autor:
frédérique AUDIC, Sonia M Dubois, Julien Durigneux, Christine Barnerias, Arnaud Isapof, Marie-Christine Nougues, Jean-Baptiste Davion, Christian Richelme, Carole Vuillerot, Laure Legoff, Pascal Sabouraud, Claude Cances, Vincent Laugel, Juliette Ropars, Caroline Espil-Taris, Valérie Trommsdorff, Anne Pervillé, Marta Gomez Garcia de la Banda, Hervé Testard, Mondher Chouchane, Ulrike Walther-Louvier, Cyril Schweizer, Cécile Halbert, Myriam Badri, Vanessa Pauly, Susana Quijano-Roy, Brigitte Chabrol, Isabelle Desguerre
Background Spinal muscular atrophy (SMA) is a rare genetic neuromuscular disorder due to an autosomal recessive mutation in the survival motor neuron 1 gene (SMN1) causing degeneration of the anterior horn cells of the spinal cord and resulting in mu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51a60df9d58b98836c9181dd6f81239c
https://doi.org/10.21203/rs.3.rs-1932236/v1
https://doi.org/10.21203/rs.3.rs-1932236/v1
