Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Duchenne muscular distrophy"'
Autor:
Crous Sala, Adriana
Publikováno v:
UPCommons. Portal del coneixement obert de la UPC
Universitat Politècnica de Catalunya (UPC)
Universitat Politècnica de Catalunya (UPC)
En aquest treball hem creat un joc seriòs basat en el controlador Leap Motion per a fer un acompanyament a la teràpia de rehabilitació que segueixen les persones amb Distròfia Muscular de Duchenne. El joc és el conegut joc de bitlles tradicional
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::437af1fa95f60413892efde5ce1fbff0
https://hdl.handle.net/2117/369082
https://hdl.handle.net/2117/369082
The Duchenne Muscular Dystrophy (DMD) and the Spinal Muscular Atrophy (SMA) are two rare neuromuscular diseases characterized by muscle weakness that lead to loss of ambulation, respiratory and cardiologic problems, and premature death1,2. Even with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3484::be8474770fedd83a5f900c0498f4adfc
https://hdl.handle.net/2117/381016
https://hdl.handle.net/2117/381016
Publikováno v:
Biblioteca Digital de Teses e Dissertações da Universidade Estadual de Campinas (UNICAMP)
Universidade Estadual de Campinas (UNICAMP)
instacron:UNICAMP
Universidade Estadual de Campinas (UNICAMP)
instacron:UNICAMP
Orientadores: Maria Julia Marques, Selma Maria Michelin Matheus Dissertação (mestrado) - Universidade Estadual de Campinas, Instituto de Biologia Resumo: A distrofia muscular de Duchenne (DMD) é uma miopatia progressiva causada pela ausência da p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79b9fd10ca26121a0f88257837ab4e27
https://doi.org/10.47749/t/unicamp.2012.878966
https://doi.org/10.47749/t/unicamp.2012.878966
Autor:
Comas Triadó, Paula
Publikováno v:
UPCommons. Portal del coneixement obert de la UPC
Universitat Politècnica de Catalunya (UPC)
Universitat Politècnica de Catalunya (UPC)
Duchenne Muscular Dystrophy (DMD) is the most common form of muscular dystrophies diagnosed during childhood, and it affects approximately 1 out in 5000 male newborns in the world [1]. This disorder causes the progressive muscle weakness and loss of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::c4fcac828d916b915dd23346cc829077
http://hdl.handle.net/2117/353076
http://hdl.handle.net/2117/353076
Autor:
Sánchez Belda, Pedro
Publikováno v:
Repositorio Institucional del Banco de España
Banco de España
Repositorio de la Escuela Universitaria Gimbernat
instname
Banco de España
Repositorio de la Escuela Universitaria Gimbernat
instname
RESUMEN : INTRODUCCIÓN. La distrofia muscular de Duchenne es una enfermedad neuromuscular de herencia recesiva que afecta a varones. Caracterizado por una progresiva debilidad muscular y posteriormente la aparición de complicaciones ocasiona discap
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::993e491427d3e8759ea52a4f05ba277d
http://hdl.handle.net/20.500.13002/836
http://hdl.handle.net/20.500.13002/836
OBJETIVO: Pacientes com distrofia muscular de Duchenne apresentam alterações neuronais em regiões do sistema nervoso central como no giro pós-central e cerebelo. Para entender a sua influência sobre o controle motor, nós investigamos a somestes
Autor:
Erica Mencarelli, Adele D'Amico, Fabrizio Drago, Rachele Adorisio, Massimo Stefano Silvetti, Marianna Cicenia, Maria Grandinetti, Liliana Amato, Antonio Amodeo, Nicoletta Cantarutti, Camilla Calvieri
Publikováno v:
Journal of Clinical Medicine, Vol 9, Iss 3186, p 3186 (2020)
Journal of Clinical Medicine
Journal of Clinical Medicine
Duchenne muscular dystrophy (DMD) cardiomyopathy (DCM) is characterized by a hypokinetic, dilated phenotype progressively increasing with age. Regular cardiac care is crucial in DMD care. Early recognition and prophylactic use of angiotensin converti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::097ff7c7943c99036015a3e5007bfb48
https://www.mdpi.com/2077-0383/9/10/3186
https://www.mdpi.com/2077-0383/9/10/3186
Autor:
PALMIERI, Beniamino, BOVOLENTA, Matteo, BRAGHETTA, Paola, CAPOBIANCO, Massimo Luigi, MARCHESI, Elena, 44121 Ferrara (IT) MEDICI, Alessandro, MOLON, Sibilla, PERRONE, Daniela, RIMESSI, Paola
Publikováno v:
WO/2020/084488, Internazionale, 2020
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::176736a67b2357babd1a3a9b7092a5c6
https://patentscope.wipo.int/search/en/detail.jsf?docId=WO2020084488&tab=FAMILY
https://patentscope.wipo.int/search/en/detail.jsf?docId=WO2020084488&tab=FAMILY
L'intérêt de l’utilisation des vecteurs viraux comme le Adeno-Associated Virus recombinant (rAAV) dans la recherche pour le traitement des maladies génétiques a conduit à une évolution rapide des méthodes de production d'AAV au cours des deu
Externí odkaz:
http://www.theses.fr/2017SACLV051/document