Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Beatriz Cassarotti"'
Autor:
Patrícia Áurea Andreucci Martins Bonilha, Beatriz Cassarotti, Thabata Emanuelle Martins Nunes, Hélio Afonso Ghizoni Teive
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 81, Iss 10, Pp 934-936 (2023)
Frontal ataxia, originally described by Bruns, is characterized by the presence of signs of frontal lobe dysfunction, such as perseveration, paratonia, frontal release signs, cognitive changes, and urinary difficulty, associated with imbalance, slow
Externí odkaz:
https://doaj.org/article/c5edfe017b6845d790263c231539b3d7
Autor:
Leo Coutinho, Otto Fustes, Thabata Nunes, Patricia Bonilha, Beatriz Cassarotti, Dafne Bayer, Alessandra Filpo, Emanuel Cassou, Helio Afonso Teive
Publikováno v:
Tuesday, April 25.
Autor:
Isabela Silva Souza, Beatriz Cassarotti, Lucas de Oliveira Pinto Bertoldi, Alana Strucker Barbosa, Eduardo Silveira Marques Branco, Isabela Badan Fernandes, Bruno Eji Nakano, Gabriel Flamarin Cavasana, Paula Carolina Grande Nakazato, Carla Ferreira dos Santos, Stella Kawano de Oliveira, Luiz Domingos Mendes Melges, Fabio de Araujo Pereira, Natalia Samadello Melges, Luiz Henrique Stefano
Publikováno v:
São Paulo Medical Journal.
Context: Fahr’s syndrome is a rare disorder characterized by bilateral and symmetrical abnormal calcifications in basal ganglia and cerebral cortex. Those calcified deposits are due to changes in calcium and phosphorus metabolisms that can be cause
Autor:
Lucas de Oliveira Pinto Bertoldi, Beatriz Cassarotti, Isabela Silva Souza, Alana Strucker Barbosa, Eduardo Silveira Marques Branco, Isabela Badan Fernandes, Paula Carolina Grande Nakazato, Gabriel Flamarin Cavasana, Bruno Eji Nakano, Carla Ferreira dos Santos, Stella Kawano de Oliveira, Nely Regina Sartori Neves, Fabio de Araujo Pereira, Natalia Samadello Melges, Luiz Henrique Stefano, Luiz Domingos Mendes Melges
Publikováno v:
São Paulo Medical Journal.
Context: Creutzfeld Jakob disease, a rare prion disease that leads to rapidly progressive dementia and movement disorders, through its pathophysiology will determine brain damage. Regardless of the cause, the course of the disease will be rapid and w
Autor:
Beatriz Cassarotti, Lucas de Oliveira Pointo Bertoldi, Alana Strucker Barbosa, Isabela Silva Souza, Eduardo Silveira Marques Branco, Carla Ferreirados Santos, Nely Regina Sartoridas Neves, Gabriel Flamarin Cavasana, Fabio de Araujo Pereira, Luiz Henrique Stefano, Natalia Samadello Melges, Luiz Domingos Mendes Melges
Publikováno v:
São Paulo Medical Journal.
Context: Dermatomyositis is an inflammatory myopathy, which results from loss of tolerance to a select group of autoantigens, with an incidence of approximately 0.8 to 1.2 per 100,000, of bimodal distribution, more frequent in women, with important r