Zobrazeno 1 - 10
of 486
pro vyhledávání: '"DA SILVA LC"'
Autor:
da Silva LC, Garcia T, Mori M, Sandri G, Bonferoni MC, Finotelli PV, Cinelli LP, Caramella C, Cabral LM
Publikováno v:
International Journal of Nanomedicine, Vol 2012, Iss default, Pp 2975-2986 (2012)
Luiz Cláudio da Silva,1 Thiago Garcia,1 Michela Mori,2 Giuseppina Sandri,2 Maria Cristina Bonferoni,2 Priscila V Finotelli,1 Leonardo P Cinelli,1 Carla Caramella,2 Lúcio M Cabral11Drug Department, Rio de Janeiro Federal University, Rio de Janeiro,
Externí odkaz:
https://doaj.org/article/c7fe7df807084d3dbf32b48b7e03ecca
Autor:
Broering MF, Oseliero Filho PL, Borges PP, da Silva LCC, Knirsch MC, Xavier LF, Scharf P, Sandri S, Stephano MA, de Oliveira FA, Sayed IM, Gamarra LF, Das S, Fantini MC, Farsky SH
Publikováno v:
International Journal of Nanomedicine, Vol Volume 19, Pp 3537-3554 (2024)
Milena Fronza Broering,1,2 Pedro Leonidas Oseliero Filho,3,4 Pâmela Pacassa Borges,1 Luis Carlos Cides da Silva,3 Marcos Camargo Knirsch,5 Luana Filippi Xavier,1 Pablo Scharf,1 Silvana Sandri,1 Marco Antonio Stephano,5 Fernando Anselmo de Oliveira,6
Externí odkaz:
https://doaj.org/article/15c21ac77e404e3882ada26191248ae8
Autor:
Celso Júlio da Silva LC
Esta obra trata argumentos filosóficos como tentativa de traçar a realidade do drama humano na fronteira do mistério de Deus. Sem a pretensão de esgotar todas as possibilidades do pensar filosófico, as intuições contidas aqui acendem um fogo d
Autor:
Celso Júlio da Silva LC
O leitor tem nas suas mãos um livro que procura mostrar a harmonia que há entre a literatura como um produto do espírito humano e a fé em Jesus Cristo. Lendo este livro, perceberá que a literatura é um caminho para chegar à contemplação de D
Autor:
da Silva Lc, Cortinhas Alves Ea, de Melo Amaral Ce, Andrade Rc, Rocha Bastos Am, Fernandes Caldato Mc
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEM. 29(1)
Primary congenital hypothyroidism (PCH) has an incidence of approximately 1 in each 3000–4000 live births. In the last two decades, nearly 50 types of the distinct inactivating mutations have already been described in the coding region of the tshr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da929bdfeac0e55958088c6a041e424b
https://pubmed.ncbi.nlm.nih.gov/26356361
https://pubmed.ncbi.nlm.nih.gov/26356361
Autor:
Patricia Martins Moura Barrios, José Carlos Soares de Fraga, Osvaldo Alfonso Pinto Artigalas, Durval Batista Palhares, Alcantara Ff, Rachel Sayuri Honjo, Chong Ae Kim, Eugênia Ribeiro Valadares, Mara Lúcia Schmitz Ferreira Santos, Laura Bannach Jardim, Miguel A. M. Moreira, de Lucca Gr, Raquel Boy, Helena Pimentel, Carmem Bonfim, Denise Y. J. Norato, Paulo Cesar Aranda, Cabral Jm, de Souza In, Cristiano de Pádua Souza, A. M. Martins, Erlane Marques Ribeiro, da Silva Lc, Marcelo Kerstenetzky, Charles Marques Lourenço, Ana Cecília Azevedo, Ronaldo C. da Costa, José Eduardo Góes, Emerson de Santana Santos, Guarany F, Nicole Ruas, Maria Verónica Muñoz Rojas, Taiane Alves Vieira, Louise Lapagesse de Camargo Pinto, Simone Fagondes, Juan C. Llerena, Correa J, Bonfim D, Angelina Xavier Acosta, Avilla Sg, Diane Ruschel Marinho, Simionato J, Dafne Dain Gandelman Horovitz, Márcia Gonçalves Ribeiro, Andressa Federhen, Roberto Giugliani, Liane de Rosso Giuliani
Publikováno v:
Genetics and Molecular Biology v.33 n.4 2010
Genetics and Molecular Biology
Sociedade Brasileira de Genética (SBG)
instacron:SBG
Genetics and Molecular Biology, Volume: 33, Issue: 4, Pages: 589-604, Published: 12 NOV 2010
Genetics and Molecular Biology, Vol 33, Iss 4, Pp 589-604 (2010)
Repositório Institucional da UnB
Universidade de Brasília (UnB)
instacron:UNB
Genetics and Molecular Biology
Sociedade Brasileira de Genética (SBG)
instacron:SBG
Genetics and Molecular Biology, Volume: 33, Issue: 4, Pages: 589-604, Published: 12 NOV 2010
Genetics and Molecular Biology, Vol 33, Iss 4, Pp 589-604 (2010)
Repositório Institucional da UnB
Universidade de Brasília (UnB)
instacron:UNB
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::241478efaf127f172c16bff10d2021f7
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572010000400001
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572010000400001
Autor:
Márcia Cristina da Costa Miguel, Bernardo Ferreira Brasileiro, Marta Rabello Piva, da Silva Lc, Paulo Ricardo Saquete Martins-Filho, Cassiano Francisco Weege Nonaka
Publikováno v:
Brasileiro, Bernardo Ferreira ; Martins Filho, Paulo R. ; Piva, Marta R. ; Silva, Luiz Carlos F. ; Nonaka, Cassiano-Francisco-Weege ; Miguel, Márcia Cristina da Costa. Myofibroma of the oral cavity. A rare spindle cell neoplasm. En: Medicina oral, patología oral y cirugía bucal. Ed. inglesa, 15 4 2010: 10
RODERIC. Repositorio Institucional de la Universitat de Valéncia
instname
RODERIC. Repositorio Institucional de la Universitat de Valéncia
instname
Myofibroma is an uncommon spindle cell neoplasm rarely found in oral cavity. Typically, this lesion is seen in neonates and infants with few cases reported in adults patients. In the oral cavity, myofibroma occurs within the submucosal or intramuscul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2c577bdf256e43b854f8359e2e4c0ab
https://pubmed.ncbi.nlm.nih.gov/20038894
https://pubmed.ncbi.nlm.nih.gov/20038894
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