Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Maria Bernadete Dutra de Resende"'
Autor:
Joyce Martini, Mariana Callil Voos, Michele Emy Hukuda, Maria Bernadete Dutra de Resende, Fátima Aparecida Caromano
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 72, Iss 1, Pp 5-11 (2014)
Objective: During the transitional phase (ambulatory to non-ambulatory), synergies characterize the evolution of Duchenne muscular dystrophy (DMD). This study was performed to describe and quantify compensatory movements while sitting down on/rising
Externí odkaz:
https://doaj.org/article/2361dc016b174547baa1a07ec362eca5
Autor:
Valdecir Antonio Simon, Edmar Zanoteli, Margarete Andreozzi Vaz Pereira Simon, Maria Bernadete Dutra de Resende, Umbertina Conti Reed
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 75, Iss 8, Pp 553-562
ABSTRACT Objective To validate the Life Satisfaction Index for Adolescents (LSI-A) scale, parent version and patient version, for Duchenne muscular dystrophy (DMD), spinal muscular atrophy (SMA) and limb-girdle muscular dystrophy (LGMD). Methods The
Externí odkaz:
https://doaj.org/article/02b12f7db18f444c97b77ee58fc9f2c0
Autor:
Craig M. McDonald, Eugenio Mercuri, Francesco Muntoni, Heather Gordish-Dressman, Lauren P. Morgenroth, Maria Bernadete Dutra de Resende, Shuizhen Zhou, Mathukumalli Lakshmi Neeharika, Kazuhiro Haginoya, Leigh Ramos-Platt, Paula Williams, Vinay Penematsa, Connie Chou, Min Lin, Shelley Johnson, Karyn Koladicz, Nicholas Mastrandrea, Christian Werner, Panayiota Trifillis
Publikováno v:
Wednesday, April 26.
Autor:
Perry B Shieh, Gary Elfring, Panayiota Trifillis, Claudio Santos, Stuart W Peltz, Julie A Parsons, Susan Apkon, Basil T Darras, Craig Campbell, Craig M McDonald, Richard J Barohn, Enrico Bertini, Kate Bushby, Brigitte Chabrol, Emma Ciafaloni, Jaume Columer, Giacomi Pietro Comi, Anne Connolly, Richard S Finkel, Kevin M Flanigan, Nathalie Goemans, Michela Guglieri, Susan T Iannaccone, Kristi J Jones, Petra Kaufmann, Janbernd Kirschner, Jean K Mah, Katherine Mathews, Eugenio Mercuri, Francesco Muntoni, Yoram Nevo, Andrés Nascimento Osorio, Yann Péréon, Rosaline Quinlivan, J. Ben Renfroe, Barry Russman, Monique Ryan, Jacinda Sampson, Ulrike Schara, Kathryn Selby, Thomas Sejersen, Douglas M Sproule, H. Lee Sweeney, Már Tulinius, Juan J Vilchez, Giuseppe Vita, Thomas Voit, Stephanie Burns-Wechsler, Brenda Wong, Ted Abresch, Erik K Henricson, Kim Coleman, Michelle Eagle, Julaine Florence, Ed Gappmaier, Craig McDonald, Hoda Z Abdel-Hamid, Clemens Bloetzer, Russell J Butterfield, Jong-Hee Chae, Jahannaz Dastgir, Isabelle Desguerre, Raul G Escobar, Erika Finanger, Peter Heydemann, Imelda Hughes, Anna Kaminska, Peter Karachunski, Martin Kudr, Timothy Lotze, Alexandra Prufer de Queiroz Campos Araujo, Maria Bernadete Dutra de Resende, Gihan Tennekoon, Haluk Topaloglu, Ricardo Erazo Torricelli, Lindsay N Alfano, Meredith K James, Linda Lowes, Anna Mayhew, Elena S Mazzone, Leslie Nelson, Kristy J Rose
Publikováno v:
Paediatrics Publications
Aim: Compare efficacies of deflazacort and prednisone/prednisolone in providing clinically meaningful delays in loss of physical milestones in patients with nonsense mutation Duchenne muscular dystrophy. Materials & methods: Placebo data from Phase I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e773db882a9b68ac18148646fe6a8d7
https://ir.lib.uwo.ca/context/paedpub/article/3206/viewcontent/843.pdf
https://ir.lib.uwo.ca/context/paedpub/article/3206/viewcontent/843.pdf
Autor:
Mariana C, Artilheiro, Cristina Dos Santos, Cardoso de Sá, Francis M, Fávero, Hanna C, Wutzki, Maria Bernadete Dutra, de Resende, Fátima A, Caromano, Mariana C, Voos
Publikováno v:
Perceptual and motor skills. 124(2)
The aim of this study was to investigate the relationship between Performance of Upper Limb (PUL) and Jebsen-Taylor Test (JTT) to assess and monitor upper limb function progression in patients with muscular dystrophy. Thirty patients diagnosed with D
Autor:
Nathalie Goemans, Perry B. Shieh, Eugenio Mercuri, M. James, Maria Bernadete Dutra de Resende, Kathryn Selby, Jean K. Mah, Brigitte Chabrol, Juan J. Vílchez, Andrés Nascimento Osorio, Yann Péréon, Linda Lowes, Gihan Tennekoon, Leslie Nelson, Jahannaz Dastgir, Janbernd Kirschner, Thomas Voit, Haluk Topaloglu, Joseph McIntosh, Marcio Souza, Francesco Muntoni, Susan D. Apkon, Richard S. Finkel, Enrico Bertini, R. Spiegel, Kristi J. Jones, Timothy Lotze, Julie A. Parsons, Peter Riebling, Kristy Rose, Giuseppe Vita, H. Kroger, Tuyen Ong, H. Lee Sweeney, Susan T. Iannaccone, Michela Guglieri, Craig Campbell, Kevin M. Flanigan, Clemens Bloetzer, Xiaohui Luo, Peter Heydemann, Michelle Eagle, Anna Kamińska, Stuart W. Peltz, Peter I. Karachunski, Martin Kudr, Giacomi Pietro Comi, Hoda Abdel-Hamid, Lausanne Canton de Vaud, Craig M. McDonald, Basil T. Darras, Yoram Nevo, Ulrike Schara, Alexandra Prufer de Queiroz Campos Araujo, Lindsay N. Alfano, Russell J. Butterfield, J. Ben Renfroe, Thomas Sejersen, Erika Finanger, Gary Elfring, Katherine D. Mathews, Jong-Hee Chae, Isabelle Desguerre, Daehak-ro Jongno-gu, Raul G Escobar, Elena S. Mazzone, Anna Mayhew, Brenda Wong, Richard J. Barohn, Monique M. Ryan, Imelda Hughes, Ricardo Erazo Torricelli, Mar Tulinius
Publikováno v:
Lancet
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
Paediatrics Publications
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
Paediatrics Publications
BACKGROUND: Duchenne muscular dystrophy (DMD) is a severe, progressive, and rare neuromuscular, X-linked recessive disease. Dystrophin deficiency is the underlying cause of disease; therefore, mutation-specific therapies aimed at restoring dystrophin
Autor:
Renata Escorcio
Publikováno v:
Biblioteca Digital de Teses e Dissertações da USP
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
OBJETIVO: Avaliar a responsividade da escala de avaliação funcional para pacientes com distrofia muscular de Duchenne (FES-DMD-D4), sentar e levantar do solo, no período de um ano. MÉTODO: Estudo observacional, longitudinal e retrospectivo. Foi e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c594feb12b537b08e0093e330f45fe1
https://doi.org/10.11606/t.5.2016.tde-20052016-163309
https://doi.org/10.11606/t.5.2016.tde-20052016-163309
Autor:
Paulo de Figueiredo Garcia
Publikováno v:
Biblioteca Digital de Teses e Dissertações da USP
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Segundo dados oficiais, há no Brasil 45 milhões de pessoas com alguma deficiência, o que corresponde a 23,5 por cento da população, este número tem crescido devido a diversos fatores, entre eles ao aumento da morbidade que acarretam deficiênci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5f0578611a4f2b05e6884029e557f79
https://doi.org/10.11606/d.6.2014.tde-04062014-133916
https://doi.org/10.11606/d.6.2014.tde-04062014-133916
Publikováno v:
Biblioteca Digital de Teses e Dissertações da USP
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
A Distrofia Muscular de Duchenne (DMD) é uma doença de herança genética recessiva que gera um quadro de fraqueza muscular progressiva muitas vezes associada à deficiência mental. A atenção, considerada como o mecanismo cerebral que permite o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31b97c79d188fd3f1df16c7a527b295e
https://doi.org/10.11606/d.47.2009.tde-31072009-151351
https://doi.org/10.11606/d.47.2009.tde-31072009-151351
Autor:
Claudia de Castro Selestrin
Publikováno v:
Biblioteca Digital de Teses e Dissertações da USP
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
A Distrofia Muscular de Duchenne (DMD) é a distrofia muscular mais comum e severa da infância, resultando em fraqueza e perda de massa muscular progressiva, que leva a múltiplas incapacidades e diminuição da sobrevivência. Os tratamentos dispon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1422ad98dd296d7fb22e4c737287654d