Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Rosa Maria R.P.S. Castro"'
Autor:
Renata Areza-Fegyveres, Sergio Rosemberg, Rosa Maria R.P.S. Castro, Claudia Sellitto Porto, Valéria Santoro Bahia, Paulo Caramelli, Ricardo Nitrini
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 65, Iss 3b, Pp 830-833 (2007)
A 61-year-old ex-boxer presented with a three-year history of progressive memory decline. During a seven-year follow-up period, there was a continuous cognitive decline, very similar to that usually observed in Alzheimer's disease. Parkinsonian, pyra
Externí odkaz:
https://doaj.org/article/bb932b3876f94364a53ac3d07a089c1f
Autor:
Ricardo Nitrini, Renata Areza-Fegyveres, Vilma R. Martins, Rosa Maria R.P.S. Castro, Michele C. Landemberger, Nancy Huang, Luiz A. Bacheschi, Luiz E. Bacheschi, Cláudia C. Leite, Carlos A. Buchpiguel, Sérgio Rosemberg
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 63, Iss 2b, Pp 519-522 (2005)
High signal in the cerebral cortex and/or basal ganglia on diffusion-weighted magnetic resonance imaging (DW-MRI) has been described as a good diagnostic marker for sporadic Creutzfeldt-Jakob disease (sCJD). We report a case of sCJD with atypical cli
Externí odkaz:
https://doaj.org/article/447acf54803f43b7b2378711ecae3ab7
Autor:
Américo Ceiki Sakamoto, Karinne Rezek, Sara Escorsi-Rosset, Roger Walz, Rosa Maria R.P.S. Castro, Vilma R. Martins, Érica R. Coimbra, Vera Cristina Terra-Bustamante, Lauro Wichert-Ana, Ricardo Guarnieri, Tonicarlo Rodrigues Velasco, Michelle N. Valadão, Ricardo R. Brentani, Marino Muxfeldt Bianchin, Veriano Alexandre, Michele Christine Landemberger
Publikováno v:
Epilepsy & Behavior. 12:210-213
a CIREP, Centro de Cirurgia de Epilepsia, Faculdade de Medicina de Ribeiaro Preto, Universidade de Sao Paulo (FMRP-USP), Ribeirao Preto, SP, Brazil b Departamento de Neurologia, Psiquiatria e Psicologia Medica, FMRP-USP, Ribeirao Preto, SP, Brazil c
Autor:
Roger Walz, Carlos Gilberto Carlotti, Rosa Maria R.P.S. Castro, Américo Ceiki Sakamoto, Vilma R. Martins, Tonicarlo Rodrigues Velasco, Ricardo R. Brentani
Publikováno v:
Cellular and Molecular Neurobiology. 22:249-257
1. Cellular prion (PrPc) is a plasma membrane protein involved with copper uptake, protection against oxidative stress, cell adhesion, differentiation, signaling, and survival in the central nervous system. 2. Deletion of PrPc gene (Pmp) in mice enha
Autor:
Paulo Caramelli, Valéria Santoro Bahia, Rosa Maria R.P.S. Castro, Cláudia Sellitto Porto, Renata Areza-Fegyveres, Sérgio Rosemberg, Ricardo Nitrini
Publikováno v:
Arquivos de Neuro-Psiquiatria v.65 n.3b 2007
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria, Volume: 65, Issue: 3b, Pages: 830-833, Published: SEP 2007
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria, Volume: 65, Issue: 3b, Pages: 830-833, Published: SEP 2007
A 61-year-old ex-boxer presented with a three-year history of progressive memory decline. During a seven-year follow-up period, there was a continuous cognitive decline, very similar to that usually observed in Alzheimer's disease. Parkinsonian, pyra
Autor:
Ricardo R. Brentani, Michele Christine Landemberger, Ricardo Guarnieri, Tonicarlo Rodrigues Velasco, Lauro Wichert-Ana, Veriano Alexandre, Américo Ceiki Sakamoto, Érica R. Coimbra, Karinne Rezek, Roger Walz, Michelle N. Valadão, Rosa Maria R.P.S. Castro, Marino Muxfeldt Bianchin, Sara Escorsi-Rosset, Vera Cristina Terra-Bustamante, Vilma R. Martins
Publikováno v:
Epilepsybehavior : EB. 8(3)
Cognitive impairment has long been recognized in people with medically refractory epilepsies. Mesial temporal lobe epilepsy related to hippocampal sclerosis (MTLE-HS), the most common surgically remediable epileptic syndrome, has been associated with
Autor:
Karina Braga Ribeiro, Marilene H. Lopes, Rosa Maria R.P.S. Castro, Gabriel L. Mancini, Ricardo R. Brentani, Rafael Linden, Glaucia N. M. Hajj, Vilma R. Martins, Angelita G. Muras
Understanding the physiological function of the cellular prion (PrPc) depends on the investigation of PrPc-interacting proteins. Stress-inducible protein 1 (STI1) is a specific PrPcligand that promotes neuroprotection of retinal neurons through cAMP-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0abfe6a77044dc2df8beeb2032c96dba
https://europepmc.org/articles/PMC6725915/
https://europepmc.org/articles/PMC6725915/
Autor:
Renata Areza-Fegyveres, Luiz Alberto Bacheschi, N. Huang, Claudia da Costa Leite, Michele Christine Landemberger, Ricardo Nitrini, Carlos Alberto Buchpiguel, Sérgio Rosemberg, Rosa Maria R.P.S. Castro, Luiz E. Bacheschi, Vilma R. Martins
Publikováno v:
Arquivos de Neuro-Psiquiatria v.63 n.2b 2005
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria, Volume: 63, Issue: 2b, Pages: 519-522, Published: JUN 2005
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria, Volume: 63, Issue: 2b, Pages: 519-522, Published: JUN 2005
High signal in the cerebral cortex and/or basal ganglia on diffusion-weighted magnetic resonance imaging (DW-MRI) has been described as a good diagnostic marker for sporadic Creutzfeldt-Jakob disease (sCJD). We report a case of sCJD with atypical cli
Autor:
A.C. Santos, Veriano Alexandre, A. Bastos, Lauro Wichert-Ana, Carlos Gilberto Carlotti, Américo Ceiki Sakamoto, Hélio Rubens Machado, Ricardo R. Brentani, M. C. Landemberger, David Araújo, Tonicarlo Rodrigues Velasco, Vilma R. Martins, Rosa Maria R.P.S. Castro, Roger Walz, Vera Cristina Terra-Bustamante, M. Bianchin
Publikováno v:
Neurology. 63(3)
Studies in animals lacking the cellular prion protein (PrP(c)) gene (Prnp) showed higher neuronal excitability in vitro and increased sensitivity to seizures in vivo. The authors previously reported a rare polymorphism at codon 171 (Asn-->Ser) of hum
Autor:
Ricardo P. Moura, Vilma R. Martins, Danielle R. Cunha, Rosa Maria R.P.S. Castro, N. Huang, Michele Christine Landemberger, Otavia L. Caballero, Ricardo Nitrini, Roger Walz, Américo Ceiki Sakamoto, Carlos Gilberto Carlotti, Ricardo R. Brentani
Publikováno v:
Journal of neuroscience methods. 139(2)
Mutations in the human prion protein gene (PRNP) are responsible for hereditary diseases called transmissible spongiform encephalopathies (TSE) and a polymorphic site at codon 129 determines sensitivity to infectious forms of these maladies. More rec