Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Laura, Jardim"'
Autor:
dos Santos, Natan Guilherme, Santos, Eduardo Fernando dos, Morari, Pedro Henrique Ribeiro, Chiarelli, Laura Jardim, Castilho-Noll, Maria Stela Maioli
Publikováno v:
In Science of the Total Environment 15 September 2023 891
Akademický článek
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Autor:
Tarsila Vieceli, Ana Laura Jardim Tavares, Renata Pibernat de Moraes, Gustavo Adolpho Moreira Faulhaber
Publikováno v:
Autopsy and Case Reports, Vol 10, Iss 4 (2021)
Neuroblastoma (NB) is a solid tumor of the sympathetic nervous system, most commonly found in childhood, standing for 7% of all pediatric malignancies. The incidence in adults is markedly smaller: 1 case per 10 million adults per year. We report the
Externí odkaz:
https://doaj.org/article/1fd75a2315a14b0faf1921833e5220ce
Autor:
Cristina Netto, Maira Burin, Laura Jardim, Marilyn Tsao, Fernanda Pereira, Ursula Matte, Roberto Giugliani, Elvino Barros, Daiana Porsch, Vagner Milani, Liana Rossato, Ane Nunes
Publikováno v:
Clinical and Biomedical Research, Vol 26, Iss 3 (2020)
Fabry disease (FD) is an X-linked inborn error of glycosphingolipid metabolism due to the deficiency of α-galactosidase A. The progressive accumulation of globotriaosylceramide (Gb3), particularly in the vascular endothelium, leads to renal, cardiac
Externí odkaz:
https://doaj.org/article/0a211f3f60a641fe933d9eaaf7a90c17
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Natan Guilherme dos Santos, Eduardo Fernando dos Santos, Pedro Henrique Ribeiro Morari, Laura Jardim Chiarelli, Maria Stela Maioli Castilho-Noll
Publikováno v:
Science of The Total Environment. 891:164031
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::50d76bc1ccd6a5bdd1e4b79131087ee3
https://doi.org/10.1016/j.scitotenv.2023.164031
https://doi.org/10.1016/j.scitotenv.2023.164031
Autor:
Maria Stela Maioli Castilho-Noll, Gilmar Perbiche-Neves, Natan Guilherme dos Santos, Leilane Talita Fatoreto Schwind, Fernando Miranda Lansac-Tôha, Alan Cleber Santos da Silva, Bianca Ramos de Meira, Ciro Yoshio Joko, Cláudio Simões de Morais-Júnior, Edissa Emi Cortez Silva, Eneida Maria Eskinazi-Sant'Anna, Felipe Rafael Oliveira, Gleice de Souza Santos, João Vitor Fonseca da Silva, Jorge Laço Portinho, Karime de Araujo-Paina, Laura Jardim Chiarelli, Leidiane Pereira Diniz, Louizi de Souza Magalhães Braghin, Luiz Felipe Machado Velho, Maria Eduarda Turcato de Souza, Mariana Lessa Carneiro da Silva, Mariane Amorim Rocha, Melissa Progênio, Natália Ferreira, Pedro Henrique Cirillo, Pedro Henrique Ribeiro Morari, Rodrigo Leite Arrieira, Tatiane Mantovano, Vanessa Gazulha, Viviane Lúcia dos Santos Almeida de Melo, André Ricardo Ghidini, Mauro de Melo Júnior, Fábio Amodêo Lansac-Tôha, Claudia Costa Bonecker, Nadson Ressyé Simões
Publikováno v:
Limnologica. :126057
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::53692a0e77e2dd31540d51ae92f09dde
https://doi.org/10.1016/j.limno.2023.126057
https://doi.org/10.1016/j.limno.2023.126057
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:
Carmen R. Vargas, Daniella de M. Coelho, Alethéa G. Barschak, Carolina F.M. de Souza, Ana C.S. Puga, Ida V.D. Schwartz, Laura Jardim, Roberto Giugliani
Publikováno v:
Genetics and Molecular Biology, Vol 23, Iss 2, Pp 261-264 (2000)
Adrenoleukodystrophy (X-ALD) is an X-linked recessively inherited peroxisomal disorder, phenotypically heterogeneous, characterized by progressive white-matter demyelination of the central nervous system and adrenocortical insufficiency. We investiga
Externí odkaz:
https://doaj.org/article/dbd9b92310834df1ac06a3f5f4610bbc
Autor:
Vieceli, Tarsila, Tavares, Ana Laura Jardim, Moraes, Renata Pibernat de, Faulhaber, Gustavo Adolpho Moreira
Publikováno v:
Autopsy and Case Reports, Volume: 10, Issue: 4, Article number: e2020181, Published: 23 NOV 2020
Neuroblastoma (NB) is a solid tumor of the sympathetic nervous system, most commonly found in childhood, standing for 7% of all pediatric malignancies. The incidence in adults is markedly smaller: 1 case per 10 million adults per year. We report the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______608::d4710e26d63dc945c123ed684909b24e
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2236-19602020000400503&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2236-19602020000400503&lng=en&tlng=en
