Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Rosana H. Scola"'
Autor:
Amanda Bombassaro, Gabriela X. Schneider, Flávia F. Costa, Aniele C. R. Leão, Bruna S. Soley, Fernanda Medeiros, Nickolas M. da Silva, Bruna J. F. S. Lima, Raffael J. A. Castro, Anamélia L. Bocca, Valter A. Baura, Eduardo Balsanelli, Vania C. S. Pankievicz, Nyvia M. C. Hrysay, Rosana H. Scola, Leandro F. Moreno, Conceição M. P. S. Azevedo, Emanuel M. Souza, Renata R. Gomes, Sybren de Hoog, Vânia A. Vicente
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Among agents of chromoblastomycosis, Fonsecaea pugnacius presents a unique type of infection because of its secondary neurotropic dissemination from a chronic cutaneous case in an immunocompetent patient. Neurotropism occurs with remarkable frequency
Externí odkaz:
https://doaj.org/article/a13fb75b2ad14f0ba521b0f6c4494f46
Autor:
Paulo José Lorenzoni, Elaine Cardoso, Ana C. S. Crippa, Charles Marques Lourenço, Fernanda Timm Seabra Souza, Roberto Giugliani, Maria Luiza Saraiva-Pereira, Salmo Raskin, Isac Bruck, Cláudia S. K. Kay, Rosana H. Scola, Lineu C.Werneck, Hélio A. G. Teive
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 72, Iss 3, Pp 214-218 (2014)
The aim of the study was to analyze a series of Brazilian patients with Niemann-Pick disease type C (NP-C). Method Correlations between clinical findings, laboratory data, molecular findings and treatment response are presented. Result The sample con
Externí odkaz:
https://doaj.org/article/a02badeda6ba48cc82dfe4d8ace2fc43
Autor:
Maurício Fernandes, Renato P. Munhoz, Paulo Eduardo Mestrinelli Carrilho, Walter O. Arruda, Paulo J. Lorenzoni, Rosana H. Scola, Lineu César Werneck, Hélio A. G. Teive
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 70, Iss 9, Pp 657-661 (2012)
Neurological disorders associated with glutamic acid decarboxylase (GAD) antibodies are rare pleomorphic diseases of uncertain cause, of which stiff-person syndrome (SPS) is the best-known. Here, we described nine consecutive cases of neurological di
Externí odkaz:
https://doaj.org/article/7babd1f7f1e644caa3c65799faeb03ea
Autor:
Paulo J. Lorenzoni, Rosana H. Scola, Cláudia S. Kamoi Kay, Sérgio F. Parolin, Lineu C. Werneck
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 68, Iss 6, Pp 849-854 (2010)
Lambert-Eaton myasthenic syndrome (LEMS) is an immune-mediated disorder of the presynaptic neuromuscular transmission, which more frequently occurs as the remote effect of a neoplasm, in the paraneoplastic form (P-LEMS), or in a non-paraneoplastic fo
Externí odkaz:
https://doaj.org/article/52e49de1d8f64bcfaaf33aaee35b82bf
Autor:
Paulo José Lorenzoni, Rosana H. Scola, Cláudia S. Kamoi Kay, Raquel C. Arndt, Aline A. Freund, Isac Bruck, Mara Lúcia S.F. Santos, Lineu C. Werneck
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 67, Iss 3a, Pp 668-676 (2009)
OBJECTIVE: The aim of the study was to analyze a series of Brazilian patients suffering from MELAS. METHOD: Ten patients with MELAS were studied with correlation between clinical findings, laboratorial data, electrophysiology, histochemical and molec
Externí odkaz:
https://doaj.org/article/e96581c88ea44204b3f9413cc6b7c9c7
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:
Ana Chrystina Crippa, Carlos Eduardo Silvado, Luciano de Paola, Rosana H. Scola, Regina Maria Fernandes, Lineu César Werneck
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 65, Iss 2A, Pp 222-227 (2007)
OBJECTIVE: To identify and quantify frontal sharp transients found in neonatal polysomnography of healthy full term newborns in each stage of the sleep-wake cycle within the first 48 hours of life. METHOD: The EEG from healthy term 32 newborns, legal
Externí odkaz:
https://doaj.org/article/b675cf67af2b45829b94e9689d444fe3
Autor:
Fabio Agertt, Ana C.S. Crippa, Paulo J. Lorenzoni, Rosana H. Scola, Isac Bruck, Luciano de Paola, Carlos E. Silvado, Lineu C. Werneck
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 65, Iss 1, Pp 157-160 (2007)
Menkes’ disease is a rare neurodegenerative disorder due to an intracellular defect of a copper transport protein. We describe a 7 months male patient who presented with seizures, hypoactivity and absence of visual contact. The investigation disclo
Externí odkaz:
https://doaj.org/article/bda2448653be46ff8787a20ab8e4d06c
Autor:
Paulo José Lorenzoni, Marcos Christiano Lange, Cláudia S.K. Kay, Luiz G.M.P. de Almeida, Hélio A.G. Teive, Rosana H. Scola, Lineu C. Werneck
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 64, Iss 1, Pp 118-121 (2006)
A síndrome da cabeça caída é causada por diminuição de força nos músculos extensores do pescoço sendo encontrada em diversas doenças neuromusculares, bem como, na esclerose lateral amiotrófica. Descrevemos o caso de três mulheres com diag
Externí odkaz:
https://doaj.org/article/b42176bcf7ad4009841fa03d863bf327
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