Zobrazeno 1 - 10 of 11 pro vyhledávání: '"Maria B. D. Resende"'
1
Akademický článek
Motor function measure scale, steroid therapy and patients with Duchenne muscular dystrophy
Autor: Elaine C. da Silva, Darlene L. Machado, Maria B. D. Resende, Renata F. Silva, Edmar Zanoteli, Umbertina C. Reed
Publikováno v: Arquivos de Neuro-Psiquiatria, Vol 70, Iss 3, Pp 191-195 (2012)
OBJECTIVE: To assess the evolution of motor function in patients with Duchenne muscular dystrophy (DMD) treated with steroids (prednisolone or deflazacort) through the Motor Function Measure (MFM), which evaluates three dimensions of motor performanc
Externí odkaz: https://doaj.org/article/d125c40cdbe6428f9324261dc2cbcb0c
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2
Duchenne muscular dystrophy: quality of life among 95 patients evaluated using the Life Satisfaction Index for Adolescents
Autor: Edmar Zanoteli, Umbertina Conti Reed, Maria B. D. Resende, Valdecir Antonio Simon, Margarete Andreozzi Vaz Pereira Simon
Publikováno v: Arquivos de Neuro-Psiquiatria, Vol 69, Iss 1, Pp 19-22 (2011)
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Arquivos de Neuro-Psiquiatria v.69 n.1 2011
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria, Volume: 69, Issue: 1, Pages: 19-22, Published: FEB 2011
The purpose of this study was to evaluate the quality of life (QoL) of patients with Duchenne muscular dystrophy (DMD) in different stages of the disease, by means of the Life Satisfaction Index for Adolescents (LSI-A). The practicality of this scale
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b44534a658da18ac04b5b82c0d451384
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2011000100005&lng=en&tlng=en
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3
Sleep and neuromuscular disorders in children
Autor: Rosana Cardoso Alves, Robert Skomro, Umbertina Conti Reed, Maria B. D. Resende, Fabio J.F.B. Souza
Publikováno v: Sleep Medicine Reviews. 13:133-148
Children suffering from neuromuscular diseases are at an increased risk of sleep-related breathing disorders (SRBD) such as obstructive sleep apnea syndrome (OSAS) and hypoventilation as well as central sleep apnea, which is frequent in these patient
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd4c2cea4e9f51d9a1442ade11fa46b7
https://doi.org/10.1016/j.smrv.2008.02.002
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4
Congenital Muscular Dystrophy with Merosin Deficiency:1H MR Spectroscopy and Diffusion-weighted MR Imaging
Autor: Claudia da Costa Leite, M. T. C Lacerda, Maria B. D. Resende, M. O. R Costa, Mary S. Carvalho, Suely Kazue Nagahashi Marie, Maria Concepcion Garcia Otaduy, L. G. Ferreira, Umbertina Conti Reed, Giovanni Guido Cerri
Publikováno v: Radiology. 235:190-196
To prospectively use hydrogen 1 ((1)H) magnetic resonance (MR) spectroscopy and apparent diffusion coefficient (ADC) maps to try to explain the discrepancy between the extensive white matter (WM) abnormalities observed at MR imaging and the relativel
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc034106403eb572efedd859c7d6dd71
https://doi.org/10.1148/radiol.2351031963
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5
Merosin-deficient congenital muscular dystrophy (CMD): a study of 25 Brazilian patients using MRI
Autor: Claudia da Costa Leite, L. G. Ferreira, J. Randy Jinkins, Umbertina Conti Reed, Maria B. D. Resende, Mary S. Carvalho, Suely Kazue Nagahashi Marie, Leandro Tavares Lucato, María M. Martín
Publikováno v: Pediatric Radiology. 35:572-579
Background: Merosin-deficient congenital muscular dystrophy (CMD) is characterized clinically by hypotonia and muscular weakness and, on imaging studies, by white matter (WM) abnormality. Objective: To evaluate MRI findings in Brazilian patients with
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88ee1a28b2ac543dc439c23803a13402
https://doi.org/10.1007/s00247-004-1398-y
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6
Congenital Muscular Dystrophy With Dropped Head Linked to the LMNA Gene in a Brazilian Cohort
Autor: Edmar Zanoteli, Anne Rutkowski, Thaís Virgínia Moura Machado Costa, Marco A.V. Albuquerque, Maria B. D. Resende, Umbertina Conti Reed, Lívia M.A. Pasqualin, Gerson Chadi, Elisângela Pereira de Souza Quedas
Publikováno v: Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Background Congenital muscular dystrophy is a clinically and genetically heterogeneous group of myopathies. Congenital muscular dystrophy related to lamin A/C is rare and characterized by early-onset hypotonia with axial muscle weakness typically pre
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aeee66ffca3369167ab5a7342d941b71
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8
Lung function monitoring in patients with duchenne muscular dystrophy on steroid therapy
Autor: Maria B. D. Resende, Celso R. F. Carvalho, Umbertina Conti Reed, Edmar Zanoteli, Darlene Lessa Machado, Elaine Cristina da Silva
Publikováno v: BMC Research Notes, Vol 5, Iss 1, p 435 (2012)
BMC Research Notes
Background Duchenne muscular dystrophy (DMD) is a sex-linked inherited muscle disease characterized by a progressive loss in muscle strength and respiratory muscle involvement. After 12 years of age, lung function declines at a rate of 6 % to 10.7 %
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c58f4d4debd5dc906b3e9b8d06854f43
https://doi.org/10.1186/1756-0500-5-435
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9
Medida de função motora, corticoterapia e pacientes com distrofia muscular de Duchenne
Autor: Maria B. D. Resende, Edmar Zanoteli, Umbertina Conti Reed, Darlene Lessa Machado, Elaine Cristina da Silva, Renata F. Silva
Publikováno v: Arquivos de Neuro-Psiquiatria v.70 n.3 2012
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria, Vol 70, Iss 3, Pp 191-195 (2012)
Arquivos de Neuro-Psiquiatria, Volume: 70, Issue: 3, Pages: 191-195, Published: MAR 2012
OBJECTIVE: To assess the evolution of motor function in patients with Duchenne muscular dystrophy (DMD) treated with steroids (prednisolone or deflazacort) through the Motor Function Measure (MFM), which evaluates three dimensions of motor performanc
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5fe97ea0066c3cbdb0420ea7487a376a
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2012000300007
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10
King-Denborough Syndrome: report of two Brazilian cases
Autor: L. G. Ferreira, Mary S. Carvalho, Suely Kazue Nagahashi Marie, Aron J. Diament, Milberto Scaff, Umbertina Conti Reed, Maria B. D. Resende
Publikováno v: Arquivos de Neuro-Psiquiatria v.60 n.3B 2002
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria, Vol 60, Iss 3B, Pp 739-741 (2002)
ResearcherID
We report on two boys aged 2 and 6 years-old respectively with dysmorphic face, ptosis, down-slanting palpebral fissures, hypertelorism, epicanthic folds, low-set ears, malar hypoplasia, micrognathia, high-arched palate, clinodactyly, palmar simian l
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84cf051ab0b7f0e05e0a566cfacdfa5e
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2002000500011
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