Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Franciele Fatima Lopes"'
Autor:
Jéssica Lamberty Faverzani, Tatiane Grazieli Hammerschmidt, Caroline Paula Mescka, Gilian Guerreiro, Franciele Fatima Lopes, Camila Aguilar Delgado, Daniella de Moura Coelho, Angela Sitta, Marion Deon, Moacir Wajner, Carmen Regla Vargas
Publikováno v:
Cell Biochemistry and Function.
Autor:
Luiza Steffens, Angela Sitta, Moacir Wajner, Dinara Jaqueline Moura, Carmen Regla Vargas, Matheus Bernardes Ferro, Leopoldo Vinicius Martins Nascimento, Franciele Fatima Lopes, Jeferson Gustavo Henn, Marion Deon, Daniella de Moura Coelho, Jéssica Lamberty Faverzani, Verônica Bidinotto Brito, Desirèe Padilha Marchetti, Gilian Guerreiro, Aline Steinmetz
Publikováno v:
Metabolic brain disease. 36(7)
Although phenylalanine (Phe) is known to be neurotoxic in phenylketonuria (PKU), its exact pathogenetic mechanisms of brain damage are still poorly known. Furthermore, much less is known about the role of the Phe derivatives phenylacetic (PAA), pheny
Autor:
Matheus Vernet Machado Bressan Wilke, Fabiano Poswar, Wyllians Vendramini Borelli, Kristiane Michelin Tirelli, Dévora Natalia Randon, Franciele Fátima Lopes, Fernanda Bender Pasetto, Fernanda Medeiros Sebastião, Gabrielle Dineck Iop, Larissa Faqueti, Layzon Antonio da Silva, Francyne Kubaski, Artur Francisco Schumacher Schuh, Roberto Giugliani, Ida Vanessa Doederlein Schwartz
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-10 (2023)
Abstract Background Parkinson’s disease (PD) is the second most common neurodegenerative disease worldwide. Its classic motor symptoms may be preceded by non-motor symptoms (NMS). Population studies have identified GBA variants as risk factors for
Externí odkaz:
https://doaj.org/article/bf6ad57cb09b45cb9daa95c408bf30fb
Autor:
Fernanda Medeiros Sebastião, Kristiane Michelin-Tirelli, Fernanda Bender, Franciele Fátima Lopes, Inamara Moraes, Francyne Kubaski, Roberto Giugliani, Maira Burin
Publikováno v:
Genetics and Molecular Biology, Vol 45, Iss 1 (2021)
Abstract The COVID-19 pandemic led to the reorganization of health care in several countries, including Brazil. Inborn Errors of Metabolism (IEM) are a group of rare and difficult to diagnose genetic diseases caused by pathogenic variants in genes th
Externí odkaz:
https://doaj.org/article/665ffbb72da64833b33fb1f99a7fb7fb