Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Louise Lapagesse Pinto"'
Autor:
Roberto Giugliani, Andressa Federhen, Maria Verônica Muñoz Rojas, Taiane Vieira, Osvaldo Artigalás, Louise Lapagesse Pinto, Ana Cecília Azevedo, Angelina Acosta, Carmen Bonfim, Charles Marques Lourenço, Kim Chong Ae, Dafne Horovitz, Denize Bonfim, Denise Norato, Diane Marinho, Durval Palhares, Emerson Santana Santos, Erlane Ribeiro, Eugênia Valadares, Fábio Guarany, Gisele Rosone de Lucca, Helena Pimentel, Isabel Neves de Souza, Jordão Correa Neto, José Carlos Fraga, José Eduardo Goes, José Maria Cabral, José Simionato, Juan Llerena Jr., Laura Jardim, Liane Giuliani, Luiz Carlos Santana da Silva, Mara L. Santos, Maria Angela Moreira, Marcelo Kerstenetzky, Márcia Ribeiro, Nicole Ruas, Patricia Barrios, Paulo Aranda, Rachel Honjo, Raquel Boy, Ronaldo Costa, Carolina Souza, Flavio F. Alcantara, Silvio Gilberto A. Avilla, Simone Fagondes, Ana Maria Martins
Publikováno v:
Genetics and Molecular Biology, Vol 33, Iss 4, Pp 589-604 (2010)
Mucopolysaccharidoses (MPS) are rare genetic diseases caused by the deficiency of one of the lysosomal enzymes involved in the glycosaminoglycan (GAG) breakdown pathway. This metabolic block leads to the accumulation of GAG in various organs and tiss
Externí odkaz:
https://doaj.org/article/605a4018d82c450a9dcc43fa4125a727
Autor:
Taiane Alves Vieira, Ida Vanessa Schwartz, Carolina Moura Souza, Ana Cecília Azevedo, Louise Lapagesse Pinto, Cristina Bitar, Roberto Giugliani
Publikováno v:
Clinical and Biomedical Research, Vol 28, Iss 2 (2008)
Several authors have described the occurrence of coarse granular cytoplasmic inclusions (the “AlderReilly Bodies”; ARB) in leukocytes of patients with Mucopolysaccharidosis VI (MPS VI; OMIM +253200). Aiming at estimating the frequency of ARB in M
Externí odkaz:
https://doaj.org/article/b3d58191753b40609768057fc49c5c44