Zobrazeno 1 - 10
of 77
pro vyhledávání: '"Helio A.G. Teive"'
Autor:
Marcos C. Lange, Vera L. Braatz, Carolina Tomiyoshi, Felipe M. Nóvak, Artur F. Fernandes, Laura N. Zamproni, Élcio J. Piovesan, Edison M. Nóvak, Helio A.G. Teive, Lineu C. Werneck
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 69, Iss 2a, Pp 212-216 (2011)
Neurological diseases are prevalent in the emergency room (ER). The aim of this study was to compare the neurological diagnoses between younger and older patients evaluated in the ER of a tertiary care hospital. METHOD: Patients admitted to the ER wh
Externí odkaz:
https://doaj.org/article/d29ce428a6a14bdca20abcced6843d15
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 65, Iss 4a, Pp 942-946 (2007)
Idiopathic Parkinson’s disease (PD) is characterized by reduced nigrostriatal and cortical dopaminergic influence, with changes in movement and, subsequently, behavioral and cognitive disturbances. We studied cognitive impairment in Parkinson’s d
Externí odkaz:
https://doaj.org/article/47ec60acb5734dcf99516197be9f2c5c
Autor:
Rosana H. Scola, Carla Carducci, Vanise G. Amaral, Paulo J. Lorenzoni, Helio A.G. Teive, Teresa Giovanniello, Lineu C. Werneck
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 65, Iss 4b, Pp 1224-1227 (2007)
Dopa-responsive dystonia (DRD) is an inherited metabolic disorder now classified as DYT5 with two different biochemical defects: autosomal dominant GTP cyclohydrolase 1 (GCH1) deficiency or autosomal recessive tyrosine hydroxylase deficiency. We repo
Externí odkaz:
https://doaj.org/article/01dcbe5625bd4222bca5f5a0d91c04f5
Autor:
Renato P. Munhoz, Helio A.G. Teive, Francisco M.B. Germiniani, Júlio C. Gerytch Jr, Daniel S. Sá, Marco A. Bittencourt, Ricardo Pasquini, Carlos H.F. Camargo, Lineu César Werneck
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 63, Iss 3a, Pp 592-596 (2005)
OBJECTIVE: To analyze the prevalence, severity and functional interference of movement disorders (MD) secondary to chronic use of cyclosporine A (CsA). METHOD: We conducted a cross-sectional study of 60 patients (58.3% male) with mean age 23.1 (3-75)
Externí odkaz:
https://doaj.org/article/a6401bc1f62f4373986d1cda5abfd686
Autor:
Renato P. Munhoz, Helio A.G. Teive, Marcus V. Della Coletta, Francisco M.B. Germiniani, Fábio M. Iwamoto, Carlos H.F. Camargo, Lineu César Werneck
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 63, Iss 2a, Pp 213-216 (2005)
BACKGROND: Blepharospasm (BS) is a form of central focal dystonia recently associated with psychiatric disorders, particularly obsessive and compulsive symptoms. Hemifacial spasm (HFS) represents a focal myoclonus with peripheral origin in the facial
Externí odkaz:
https://doaj.org/article/da23015d32fc4383aeedf20b40b90f72
Autor:
Marcos Christiano Lange, Viviane Flumignan Zétola, Helio A.G. Teive, Rosana H. Scola, Ana Paula Trentin, Jorge A. Zavala, Eduardo R. Pereira, Salmo Raskin, Lineu C. Werneck, Erik A. Sistermans
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 62, Iss 4, Pp 1085-1089 (2004)
Cerebrotendinous xanthomatosis is a treatable rare autossomal recessive disease characterized by lipid storage secondary to a sterol 27-hydroxylase deficiency in the formation of cholic and chenodeoxycholic acids. We describe two Brazilian brothers w
Externí odkaz:
https://doaj.org/article/56e0d04503104a74862d3b02b083cfc8
Autor:
Francisco Manoel B. Germiniani, Mauricio Roriz, Samir K. Nabhan, Helio A.G. Teive, Lineu C. Werneck
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 60, Iss 4, Pp 1030-1033 (2002)
A mielinólise pontina central (MPC) e extra-pontina (MEP) é enfermidade desmielinizante do encéfalo associada principalmente com a correção rápida da hiponatremia, que se manifesta principalmente por tetraparesia espástica e paralisia pseudo-b
Externí odkaz:
https://doaj.org/article/108bae5d36f746979bf2797af7ac78f4
Autor:
Maria Thereza D. Gama, Pedro Braga‐Neto, Deborah M. Rangel, Clécio Godeiro, Rodrigo Alencar, Emília K. Embiruçu, Mario Cornejo‐Olivas, Elison Sarapura‐Castro, Paula Saffie Awad, Daniela Muñoz Chesta, Marcelo Kauffman, Sergio Rodriguez‐Quiroga, Laura B. Jardim, Felipe F. da Graça, Marcondes C. França, Pedro J. Tomaselli, Wilson Marques, Helio A.G. Teive, Orlando G.P. Barsottini, José Luiz Pedroso, Matthis Synofzik
Publikováno v:
Movement disorders 37(8), 1773-1774 (2022). doi:10.1002/mds.29046
Autosomal recessive cerebellar ataxias (ARCAs) comprisecomplex genetic ataxia disorders with variable central andperipheral nervous system involvement and systemic changes.They can overlap with other conditions such as hereditary spas-tic paraplegia,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbd2112354b1dde02933238d94744cfd
Autor:
Gustavo L. Franklin, Hélio A.G. Teive
Publikováno v:
Brazilian Journal of Psychiatry, Vol 43, Iss 2, Pp 222-222 (2020)
Externí odkaz:
https://doaj.org/article/47aa9ffddfc34b619e70f9c4dfa73edc
Autor:
Adriana Moro, Renato P. Munhoz, Walter O. Arruda, Salmo Raskin, Mariana Moscovich, Hélio A.G. Teive
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 72, Iss 9, Pp 659-662 (2014)
Spinocerebellar ataxia type 3 (SCA3) involves cerebellar, pyramidal, extrapyramidal, motor neuron and oculomotor systems with strong phenotypic heterogeneity, that lead us to classify the disorder into different clinical subtypes according to the pre
Externí odkaz:
https://doaj.org/article/14fce1d8b73d4321b216e62f57484cd6