Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Maria Teresinha de Oliveira Cardoso"'
Autor:
Janinne Barboza Rangel, Wallace William da Silva Meireles, Ana Carolina Rathsam Leite, Cristina Touguinha Neves Medina, Maria Teresinha de Oliveira Cardoso, Romina Soledad Heredia Garcia Silva
Publikováno v:
Residência Pediátrica, Vol 14, Iss 1 (2024)
Familial chylomicronemia syndrome (FCS) is a rare, autosomal recessive monogenic disease, affecting 1:1,000,000000. A hallmark of the disease is the severe hypertriglyceridemia caused by either lipoprotein lipase (LPL) enzyme deficiency or one of its
Externí odkaz:
https://doaj.org/article/6478d961b7774952a163a6f40baa426b
Autor:
Adrielle da Silva Fachini, Lorena Freitas Barros Malaquias, Luma de Lira Nogueira, Ludmila Alvim Gomes Pinho Giacone, Noemia Urruth Leão Tavares, Maria Teresinha de Oliveira Cardoso, Guilherme Martins Gelfuso, Dayde Lane Mendonça da Silva, Rafael Santos Santana
Publikováno v:
Brazilian Journal of Pharmaceutical Sciences. 59
Autor:
Rafael Hencke Tresbach, Fernanda Sperb-Ludwig, Rodrigo Ligabue-Braun, Tássia Tonon, Maria Teresinha de Oliveira Cardoso, Romina Soledad Heredia, Maria Teresa Alves da Silva Rosa, Bárbara Cátia Martins, Monique Oliveira Poubel, Luiz Carlos Santana da Silva, François Maillot, Ida Vanessa Doederlein Schwartz
Publikováno v:
Genes, Vol 12, Iss 1, p 20 (2020)
Phenylketonuria (PKU) is a common inborn error of amino acid metabolism in which the enzyme phenylalanine hydroxylase, which converts phenylalanine to tyrosine, is functionally impaired due to pathogenic variants in the PAH gene. Thirty-four Brazilia
Externí odkaz:
https://doaj.org/article/e83e957fe3624e9db407ebd4b53f008e
Autor:
João Rocha Vilela, Maria Teresinha de Oliveira Cardoso, José Gonçalves Franco Júnior, Anaglória Pontes
Publikováno v:
Revista Brasileira de Ginecologia e Obstetrícia, Vol 34, Iss 3, Pp 122-127 (2012)
OBJETIVO: Comparar a acurácia diagnóstica da histerossonografia (HSN) com a da ultrassonografia transvaginal convencional (USG) na avaliação da cavidade uterina de mulheres inférteis candidatas às técnicas de reprodução assistida (TRA). MÉT
Externí odkaz:
https://doaj.org/article/9368205c82d14c049aa0c0c9130c9518
Autor:
Octavio L. Franco, Felipe Albuquerque Marques, Huri Brito Pogue, Állan S. Pires, Maria Gabriela Rodrigues do Vale, Maria Teresinha de Oliveira Cardoso, Robert Pogue, Sérgio Amorim de Alencar, William F. Porto
Publikováno v:
Journal of Cellular Biochemistry. 118:4762-4771
Mutations in the growth hormone receptor (GHR) gene can cause disruption of the growth hormone signaling pathway, resulting in growth deficiency due to growth hormone (GH) resistance. Both recessive and apparently dominant mutations have been describ
Autor:
Ida Vanessa Doederlein Schwartz, François Maillot, Tássia Tonon, Luiz Carlos Santana da Silva, Romina Soledad Heredia, Rodrigo Ligabue-Braun, Fernanda Sperb-Ludwig, Rafael Hencke Tresbach, Maria Teresinha de Oliveira Cardoso, Maria Teresa Alves da Silva Rosa, Bárbara Cátia Martins, Monique Oliveira Poubel
Publikováno v:
Genes
Genes, Vol 12, Iss 20, p 20 (2021)
Volume 12
Issue 1
Genes, Vol 12, Iss 20, p 20 (2021)
Volume 12
Issue 1
Phenylketonuria (PKU) is a common inborn error of amino acid metabolism in which the enzyme phenylalanine hydroxylase, which converts phenylalanine to tyrosine, is functionally impaired due to pathogenic variants in the PAH gene. Thirty-four Brazilia
Autor:
Paulo Roberto Margotto, Aline Saliba de Faria, Evely Mirella Santos França, Talyta Matos Canó, Cristina Touguinha Neves Medina, Maria Teresinha de Oliveira Cardoso, Carlos A. M. Zaconeta, Renata Lazari Sandoval
Publikováno v:
Revista Paulista de Pediatria
Repositório Institucional da UnB
Universidade de Brasília (UnB)
instacron:UNB
Revista Paulista de Pediatria, Vol 34, Iss 3, Pp 374-378
Repositório Institucional da UnB
Universidade de Brasília (UnB)
instacron:UNB
Revista Paulista de Pediatria, Vol 34, Iss 3, Pp 374-378
Objetivo: relatar caso de neonato com episódios de apneias recorrentes, diagnosticado com síndrome de hipoventilação central congênita (SHCC) associada à doença de Hirschsprung (DH), o que configurou síndrome de Haddad. Descrição do caso: t
Autor:
Renata Lazari Sandoval, Evely Mirella Santos França, Cristina Touguinha Neves Medina, Maria Teresinha de Oliveira Cardoso, Aline Saliba de Faria, Paulo Roberto Margotto, Carlos A. M. Zaconeta, Talyta Matos Canó
Publikováno v:
Revista Paulista de Pediatria. 34:374-378
ResumoObjetivoRelatar caso de neonato com episódios de apneias recorrentes, diagnosticado com síndrome de hipoventilação central congênita (SHCC) associada à doença de Hirschsprung (DH), o que configurou síndrome de Haddad.Descrição do caso
Autor:
Robert Pogue, Rosangela Vieira Andrade, Alessandra Maria Moreira Reis, Isabela C. C. Cardoso, Maria Teresinha de Oliveira Cardoso, Mayara C. B. Silva, Rinaldo Wellerson Pereira, Cristina Touguinha Neves Medina, Camila Fernandes, Daniel L. Polla, Rosenelle Araujo
Publikováno v:
PLoS ONE
PLoS ONE, Vol 10, Iss 9, p e0138314 (2015)
Web of Science
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
PLoS ONE, Vol 10, Iss 9, p e0138314 (2015)
Web of Science
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Made available in DSpace on 2018-11-26T16:17:02Z (GMT). No. of bitstreams: 0 Previous issue date: 2015-09-18 Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) Fundacao de Apoio a Pesquisa do Distrito Federal Coordenação de Aper
Autor:
Hitomi Miura Nakagawa, José Carlos Peraçoli, Bruno Ramalho de Carvalho, Maria Teresinha de Oliveira Cardoso, David Barreira Gomes-Sobrinho, Carlos Portocarrero-Sanchez, Nathália Travassos Sarkis, Adelino Amaral Silva
Publikováno v:
Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology. 31(5)
Objective: To investigate the follicular size at spontaneous rupture on pregnancy rate in patients with polycystic ovary syndrome (PCOS) undergoing clomiphene citrate (CC) ovulation.Design: Cross-sectional study.Patients and methods: One hundred and