Zobrazeno 1 - 10
of 30
pro vyhledávání: '"UMBERTINA C. REED"'
Autor:
André M. S. Silva, Antônio R. Coimbra-Neto, Paulo Victor S. Souza, Pablo B. Winckler, Marcus V. M. Gonçalves, Eduardo B. U. Cavalcanti, Alzira A. D. S. Carvalho, Cláudia F. D. R. Sobreira, Clara G. Camelo, Rodrigo D. H. Mendonça, Eduardo D. P. Estephan, Umbertina C. Reed, Marcela C. Machado-Costa, Mario E. T. Dourado-Junior, Vanessa C. Pereira, Marcelo M. Cruzeiro, Paulo V. P. Helito, Laís U. Aivazoglou, Leonardo V. D. Camargo, Hudson H. Gomes, Amaro J. S. D. Camargo, Wladimir B. V. D. R. Pinto, Bruno M. L. Badia, Luiz H. Libardi, Mario T. Yanagiura, Acary S. B. Oliveira, Anamarli Nucci, Jonas A. M. Saute, Marcondes C. França-Junior, Edmar Zanoteli
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 6, Iss 7, Pp 1225-1238 (2019)
Abstract Objective ANO5‐related myopathy is an important cause of limb‐girdle muscular dystrophy (LGMD) and hyperCKemia. The main descriptions have emerged from European cohorts, and the burden of the disease worldwide is unclear. We provide a de
Externí odkaz:
https://doaj.org/article/9569ce804f2d459a98f49ce1fbcc02cb
Autor:
Marco A. V. Albuquerque, Osório Abath-Neto, Jéssica R. Maximino, Gerson Chadi, Edmar Zanoteli, Umbertina C. Reed
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 72, Iss 10, Pp 768-772 (2014)
Patients with sarcoglycanopathies, which comprise four subtypes of autosomal recessive limb-girdle muscular dystrophies, usually present with progressive weakness leading to early loss of ambulation and premature death, and no effective treatment is
Externí odkaz:
https://doaj.org/article/391de5f9b85c4be8aedfebdff44874a3
Autor:
Felippe Borlot, Mara Lucia F. Santos, Marcia Bandeira, Paulo B. Liberalesso, Fernando Kok, Alfredo Löhr Jr., Umbertina C. Reed
Publikováno v:
Jornal de Pediatria, Vol 88, Iss 3, Pp 275-278 (2012)
OBJETIVO: Discutir o diagnóstico diferencial das encefalites além daquelas de etiologia infecciosa, e alertar os pediatras para a possibilidade do diagnóstico de encefalite anti-receptor N-metil-D-aspartato (rNMDA) na população pediátrica, dest
Externí odkaz:
https://doaj.org/article/61495fcb29f846daa49a28ea43927df2
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
Autor:
Cristiana Bolfer, Erasmo Barbante Casella, Marcus Vinícius Chrysóstomo Baldo, Amanda Manzini Mota, Miriam Harumi Tsunemi, Sandra Pasquali Pacheco, Umbertina C. Reed
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 68, Iss 2, Pp 282-286 (2010)
Attention deficit, impulsivity and hyperactivity are the cardinal features of attention deficit hyperactivity disorder (ADHD) but executive function (EF) disorders, as problems with inhibitory control, working memory and reaction time, besides others
Externí odkaz:
https://doaj.org/article/74a9db9f607e46928722ae2e92c01abc
Autor:
Karina Takata, Emerson L. Gasparetto, Claudia da Costa Leite, Leandro T. Lucato, Umbertina C. Reed, Hamilton Matushita, Paulo Henrique P. de Aguiar, Sérgio Rosemberg
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 65, Iss 2A, Pp 313-316 (2007)
OBJETIVO: Relatar os achados de ressonância magnética (RM) em 10 casos de astrocitoma subependimário de células gigantes (ASCG) em pacientes com esclerose tuberosa (ET). MÉTODO: Foram estudados de forma retrospectiva 10 pacientes com ET e diagn
Externí odkaz:
https://doaj.org/article/00e3bf27d45d4991bff043725aee3f0f
Autor:
MARILISA M. GUERREIRO, MARIA LUIZA G. MANREZA, ANNA ELISA SCOTONI, E.A. SILVA, CARLOS A. M. GUERREIRO, E.A.P. SOUZA, V.B. FERREIRA, UMBERTINA C. REED, ARON DIAMENT, R. TREFIGLIO, H.C. CHIU, J. BACALTCHUK
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 57, Iss 2A, Pp 167-175 (1999)
We conducted an open, add-on study with topiramate (TPM) as adjunctive therapy in Lennox-Gastaut syndrome (LGS), to assess the long-term efficacy and safety and to evaluate quality of life (QL) measurements in the chronic use of TPM. We studied 19 pa
Externí odkaz:
https://doaj.org/article/147d19c22fe741b785cd986970de7ef8
Autor:
Helga C. A. Azevedo, Lúcia I. Z. Mendonça, Paulo N. B. Salum, Mary S. Carvalho, Sueli K. Nagahashi-Marie, Alzira A. Siqueira-Carvalho, Maria A. Cerqueira, Umbertina C. Reed, José A. Levy
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 54, Iss 4, Pp 595-600 (1996)
Miotonia é o fenômeno da diminuição da velocidade de relaxamento muscular após contração, estímulo mecânico ou elétrico. As miotonias congênitas são afecções hereditárias e não apresentam distrofia muscular. Atualmente, a tendência
Externí odkaz:
https://doaj.org/article/5346dae2ce0f4bf09d59b9d46022fbc0
Autor:
Umbertina C. Reed, Suely K. Nagahashi Marie, Mario Wilson I. Brotto, Carlos Alberto Martinez, Paulo E. Marchiori, Aron Diament, José Antonio Levy
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 53, Iss 1, Pp 114-117 (1995)
We describe the case of a girl with a probable autosomal recessive form of nondystrophic hereditary myotonia whose clinical findings are more compatible with the dominant ones mainly myotonia congenita of Thomsen or myotonia fluctuans. Besides the cl
Externí odkaz:
https://doaj.org/article/3b5b3778a8c54673a213a94a0f8b52c3
Autor:
Umbertina C. Reed, Maria Rita Passos-Bueno, Suely K. Nagahashi-Marie, Antonia Cerqueira, Lucia I.Z. Mendonça, José Antonio Levy, Aron Diament, Mayana Zatz
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 52, Iss 4, Pp 545-548 (1994)
É relatado o caso de um paciente com início da sintomatologia aos 7 anos de idade, cujo estudo genético e o de seu pai, portador assintomático, revelou um fragmento adicional de DNA, maior no paciente sintomático do que no pai portador. Os dados
Externí odkaz:
https://doaj.org/article/b57338341c224db1bb86768f281743cb