Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Imelda De Groot"'
Autor:
Vandana Ayyar Gupta, Jacqueline M Pitchforth, Joana Domingos, Deborah Ridout, Mario Iodice, Catherine Rye, Mary Chesshyre, Amy Wolfe, Victoria Selby, Anna Mayhew, Elena S Mazzone, Valeria Ricotti, Jean-Yves Hogrel, Erik H Niks, Imelda de Groot, Laurent Servais, Volker Straub, Eugenio Mercuri, Adnan Y Manzur, Francesco Muntoni, iMDEX Consortium and the U.K. NorthStar Clinical Network
Publikováno v:
PLoS ONE, Vol 18, Iss 4, p e0283669 (2023)
The North Star ambulatory assessment (NSAA) is a functional motor outcome measure in Duchenne muscular dystrophy (DMD), widely used in clinical trials and natural history studies, as well as in clinical practice. However, little has been reported on
Externí odkaz:
https://doaj.org/article/21885a505e0b4afe9114a65409bbe906
Autor:
Giorgia Coratti, Marika Pane, Claudia Brogna, Valeria Ricotti, Sonia Messina, Adele D'Amico, Claudio Bruno, Gianluca Vita, Angela Berardinelli, Elena Mazzone, Francesca Magri, Federica Ricci, Tiziana Mongini, Roberta Battini, Luca Bello, Elena Pegoraro, Giovanni Baranello, Stefano C Previtali, Luisa Politano, Giacomo P Comi, Valeria A Sansone, Alice Donati, Jean Yves Hogrel, Volker Straub, Silvana De Lucia, Erik Niks, Laurent Servais, Imelda De Groot, Mary Chesshyre, Enrico Bertini, Nathalie Goemans, Francesco Muntoni, Eugenio Mercuri, on behalf on the International DMD Group and the iMDEX Consortium
Publikováno v:
PLoS ONE, Vol 16, Iss 6, p e0253882 (2021)
IntroductionThe aim of this study was to report 36-month longitudinal changes using the North Star Ambulatory Assessment (NSAA) in ambulant patients affected by Duchenne muscular dystrophy amenable to skip exons 44, 45, 51 or 53.Materials and methods
Externí odkaz:
https://doaj.org/article/be2f7562560244a9a2a56400fc1fd6e8
Autor:
Marlous Schnackers, Laura Beckers, Yvonne Janssen-Potten, Pauline Aarts, Eugène Rameckers, Jan van der Burg, Imelda de Groot, COAD Focus Group, Rob Smeets, Sander Geurts, Bert Steenbergen
Publikováno v:
BMC Pediatrics, Vol 18, Iss 1, Pp 1-9 (2018)
Abstract Background Home-based training is considered an important intervention in rehabilitation of children with unilateral cerebral palsy. Despite consensus on the value of home-based upper limb training, no evidence-based best practice exists. Pr
Externí odkaz:
https://doaj.org/article/34a48555459d49ab9475e91d09396ed0
Autor:
Esther Steultjens, Marieke Lindenschot, Sanne Diepeveen, Jana Zajec, Imelda de Groot, Ria Nijhuis‐van der Sanden, Saskia Koene, Maud Graff
Publikováno v:
Australian Occupational Therapy Journal, 70, 175-189
Australian Occupational Therapy Journal, 1-15
STARTPAGE=1;ENDPAGE=15;ISSN=0045-0766;TITLE=Australian Occupational Therapy Journal
Australian Occupational Therapy Journal, 70, 2, pp. 175-189
Australian Occupational Therapy Journal, 1-15
STARTPAGE=1;ENDPAGE=15;ISSN=0045-0766;TITLE=Australian Occupational Therapy Journal
Australian Occupational Therapy Journal, 70, 2, pp. 175-189
Contains fulltext : 291778.pdf (Publisher’s version ) (Open Access) INTRODUCTION: Uncovering the perspective of children with multiple disabilities is important in health care to enable person-centred health care. For occupational therapists, uncov
Autor:
Karen Anthony, Pierpaolo Ala, Francesco Catapano, Jinhong Meng, Joana Domingos, Mark Perry, Valeria Ricotti, Kate Maresh, Lauren C. Phillips, Laurent Servais, Andreea M. Seferian, Silvana De Lucia, Imelda de Groot, Yvonne D. Krom, J.G.M. Verschuuren, Erik H. Niks, Volker Straub, Michela Guglieri, Thomas Voit, Jennifer Morgan, Francesco Muntoni
Publikováno v:
Human Gene Therapy, 34, 439-448
Human Gene Therapy, 34, 9-10, pp. 439-448
Human Gene Therapy, 34, 9-10, pp. 439-448
Item does not contain fulltext Duchenne muscular dystrophy (DMD) is caused by the lack of dystrophin, but many patients have rare revertant fibers that express dystrophin. The skeletal muscle pathology of DMD patients includes immune cell infiltratio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49514bd8301473406d57fff0a578efbe
https://doi.org/10.1089/hum.2022.166
https://doi.org/10.1089/hum.2022.166
Autor:
Victor, Ronald G, Sweeney, H. Lee, Finkel, Richard, Mcdonald, Craig M, Byrne, Barry, Eagle, Michelle, Goemans, Nathalie, Vandenborne, Krista, Dubrovsky, Alberto L, Topaloglu, Haluk, Miceli, M. Carrie, Furlong, Pat, Landry, John, Elashoff, Robert, Cox, David, Hoda, Abdel-Hamid, Susan, Apkon, Richard, Barohn, Elena, Belousova, Enrico, Bertini, John, Brandsema, Claudio, Bruno, William, Burnette, Russell, Butterfield, Barry, Byrne, Craig, Campbell, Jose, Carlo, Jong-Hee, Chae, Saleel, Chandratre, Giacomo, Comi, Anne, Connolly, Imelda De Groot, Nicolas, Deconinck, Joseph, Dooley, Alberto, Dubrovsky, Julien, Durigneux, Erika, Finanger, Richard, Finkel, L Matthew Frank, Nathalie, Goemans, Amy, Harper, Ayako, Hattori, Ozlem, Herguner, Susan, Iannaccone, Joanne, Janas, Yuh-Jyh, Jong, Janberd, Kirschner, Hirofumi, Komaki, Nancy, Kuntz, Wang-Tso, Lee, Edward, Leung, Jean, Mah, Katherine, Mathews, Craig, Mcdonald, Eugenio, Mercuri, Hugh, Mcmillan, Wolfgang, Mueller-Felber, Adolfo Lopez de Munain, Akinori, Nakamura, Erik, Niks, Katsuhisa, Ogata, Samuel, Pascual, Pegoraro, Elena, Yann, Pereon, Ben, Renfroe, Ratna Bhavaraju Sanka, Jens, Schallner, Ulrike, Schara, Kathryn, Selby, Isabel Illa Sendra, Laurent, Servais, Edward, Smith, Susan, Sparks, Haluk, Topaloglu, Ron, Victor, Juan Jose Vilchez, Matthew, Wicklund, Ekkehard, Wilichoswki, Brenda, Wong
Publikováno v:
Neurology, vol 89, iss 17
Neurology
Neurology, 89(17), 1811-1820
Neurology, 89 (17
Neurology
Neurology, 89(17), 1811-1820
Neurology, 89 (17
To conduct a randomized trial to test the primary hypothesis that once-daily tadalafil, administered orally for 48 weeks, lessens the decline in ambulatory ability in boys with Duchenne muscular dystrophy (DMD).
info:eu-repo/semantics/published
info:eu-repo/semantics/published
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e0e6503a882dfb553f43c58e0475c30
https://ora.ox.ac.uk/objects/uuid:07acefc6-f3c1-43d6-aaff-dd314f53221c
https://ora.ox.ac.uk/objects/uuid:07acefc6-f3c1-43d6-aaff-dd314f53221c
Autor:
John P. Bourke, Michela Guglieri, Denis Duboc, Annemieke Aartsma-Rus, Alykhan Bandali, Neil Bennett, Bjorn Cools, Linda Cripe, Imelda de Groot, Sven Dittrich, Anca Florian, Pat Furlong, Nathalie Goemans, Kan Hor, Frank van Leperen, Guy MacGowan, Elizabeth McNally, Elena Pegoraro, Luisa Politano, Marie Sediva, Veronika Stara, Janneke Timmermans, Elizabeth Vroom, Karim Wahbi
Publikováno v:
Neuromuscular Disorders, 29(8), 634-643. PERGAMON-ELSEVIER SCIENCE LTD
Neuromuscular Disorders, 29, 634-643
Neuromuscular Disorders, 29, 8, pp. 634-643
Neuromuscular Disorders, 29, 634-643
Neuromuscular Disorders, 29, 8, pp. 634-643
Contains fulltext : 209413.pdf (Publisher’s version ) (Closed access)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6fc1729eaad5131fe0814bf4b48b3b1
http://hdl.handle.net/1887/122240
http://hdl.handle.net/1887/122240
Autor:
Arjen Bergsma, Joan Lobo-Prat, Elizabeth Vroom, Pat Furlong, Just L. Herder, Madeline Corrigan, Imelda de Groot, Aldo Faisal, Nathalie Goemans, Jay Han, Just Herder, Mario Iodice, Annie Kennedy, Bart Koopman, Joan Lobo Prat, Marion Main, Blake Mathie, Francesco Muntoni, Miguel Nobre Castro, Micha Paalman, John Porter, Tariq Rahman, Joel Schneider, Arno Stienen, Paul Verstegen, Conor Walsh
Publikováno v:
Neuromuscular disorders, 26(6), 386-393. Elsevier
Autor:
Volker Straub, Eugenio Mercuri, Annemieke Aartsma-Rus, Dimitrios Athanasiou, Pavel Balabanov, Filippo Buccella, Didier Caizergues, Pierre Carlier, Emily Crossley, Anne M. Connolly, Tina Duong, Dirk Fischer, Pat Furlong, Nathalie Goemans, Imelda de Groot, Michela Guglieri, Erik Henricson, Alex Johnson, Hermien E. Kan, Anna Mayhew, Elena Mazzone, Craig M. McDonald, Francesco Muntoni, Erik H. Niks, Laurent Servais, Cathy Turner, Thomas Voit, Elizabeth Vroom, Glenn Walter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc1e491810fb17a49e60a4828e4e2c1f
http://hdl.handle.net/10807/125807
http://hdl.handle.net/10807/125807
Autor:
Deborah Ridout, Merel Jansen, Thomas Voit, Erik H. Niks, Volker Straub, Menno Van der Holst, Laurent Servais, Imelda de Groot, Michela Guglieri, Joana Domingos, Anna Mayhew, V. Selby, Francesco Muntoni, Michelle Eagle, Valeria Ricotti, Jean-Yves Hogrel, J. Verschuuren, J. Butler, Valérie Decostre, Amélie Moraux
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 88:A63.1-A63
Background The need for deeper understanding of Duchenne muscular dystrophy (DMD) natural history is supported by the rapid advances in translational research, the increase in clinical trials and outcome of recent studies. Aim Assess the natural hist