Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Luciana Ribeiro"'
Autor:
Lívia Azeredo Alves Antunes, Karla Bianca Fernandes Da Costa Fontes, Laís Veiga Faria, Liz Helena Moraes Pinheiro, Caio Luiz Bitencourt Reis, Jéssica Agathá Coelho Homem Dias, Leonardo Santos Antunes, Marlus Roberto Rodrigues Cajazeira, Luciana Ribeiro Reis Pio
Publikováno v:
International Journal of Paediatric Dentistry. 32:585-597
Background Antimicrobial photodynamic therapy (aPDT) has been used as adjunct treatment of deep caries lesions however the effects on the longevity of restorations are still limited. Aim to evaluate the performance of composite restorations in primar
Autor:
Elaine Valim Camarinha Marcos, Hugo Vicentin Alves, Vinicius M. Fava, Jeane Eliete Laguila Visentainer, Luciana Ribeiro Jarduli, Victor Hugo de Souza, Ana Carla Pereira, Fabiana Covolo de Souza, Ida Maria Foschiani Dias-Baptista, Marcos Virmond, Milton Ozório Moraes, Priscila Verchai Uaska Sartori, Marcelo Távora Mira
Publikováno v:
International Journal of Immunogenetics. 48:25-35
Leprosy is a prevalent disease in Brazil, which ranks as the country with the second highest number of cases in the world. The disease manifests in a spectrum of forms, and genetic differences in the host can help to elucidate the immunopathogenesis.
Autor:
Luciana Ribeiro, Sabine Krüger Truppel, Mario C. Vieira, Gabriela Guimarães Vieira, Nelson Augusto Rosário Filho
Publikováno v:
Jornal de Pediatria v.96 n.5 2020
Jornal de Pediatria
Sociedade Brasileira de Pediatria (SBP)
instacron:SBPE
Jornal de Pediatria, Vol 96, Iss 5, Pp 638-643 (2020)
Jornal de Pediatria (Versão em Português), Vol 96, Iss 5, Pp 638-643 (2020)
Jornal de Pediatria, Volume: 96, Issue: 5, Pages: 638-643, Published: 11 NOV 2020
Jornal de Pediatria
Sociedade Brasileira de Pediatria (SBP)
instacron:SBPE
Jornal de Pediatria, Vol 96, Iss 5, Pp 638-643 (2020)
Jornal de Pediatria (Versão em Português), Vol 96, Iss 5, Pp 638-643 (2020)
Jornal de Pediatria, Volume: 96, Issue: 5, Pages: 638-643, Published: 11 NOV 2020
Objective: To compare endoscopic and histologic features of pediatric patients with eosinophilic esophagitis (EoE) responding to proton pump inhibitor (PPI) to those not responding to PPI. Methods: Endoscopic reports and photographs of patients with
Autor:
Sabine Krüger Truppel, Elizabeth Schneider Gugelmin, Nelson Augusto Rosário Filho, Gabriela Guimarães Vieira, Mario C. Vieira, Melyssa Grignet Ribeiro, Ana Paula Percicote, Renata Augusta de Miranda, Luciana Ribeiro
Publikováno v:
Jornal de Pediatria, Volume: 98, Issue: 1, Pages: 26-32, Published: 14 FEB 2022
Jornal de Pediatria, Vol 98, Iss 1, Pp 26-32 (2022)
Jornal de Pediatria v.98 n.1 2022
Jornal de Pediatria
Sociedade Brasileira de Pediatria (SBP)
instacron:SBPE
Jornal de Pediatria, Vol 98, Iss 1, Pp 26-32 (2022)
Jornal de Pediatria v.98 n.1 2022
Jornal de Pediatria
Sociedade Brasileira de Pediatria (SBP)
instacron:SBPE
Objective To assess intra- and interobserver agreement among non-expert pathologists in identifying features of the eosinophilic esophagitis histologic scoring system (EoEHSS) in pediatric patients. Patients and methods The authors used 50 slides fro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dab6a9caa2c3145f3678bdd2ec4d1012
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0021-75572022000100026&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0021-75572022000100026&lng=en&tlng=en
Akademický článek
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Autor:
Raquel Corripio, José I Labarta, Lourdes Travieso-Suárez, Ana Pinheiro Machado Canton, Leandro Soriano-Guillén, Jesús Argente, Maira Piovesan, Vinicius Nahime Brito, Ana Claudia Latronico, Carlos Eduardo Seraphim, Vicente Barrios, Luciana Ribeiro Montenegro, Álvaro Martín-Rivada
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 105:3165-3172
Background Central precocious puberty (CPP) has been associated with loss-of-function mutations in 2 paternally expressed genes (MKRN3 and DLK1). Rare defects in the DLk1 were also associated with poor metabolic phenotype at adulthood. Objective Our
Autor:
Nathalia Lisboa Gomes, Rafael Loch Batista, Mirian Y Nishi, Antônio Marcondes Lerário, Thatiana E Silva, Amanda de Moraes Narcizo, Anna Flávia Figueredo Benedetti, Mariana Ferreira de Assis Funari, José Antônio Faria Junior, Daniela Rodrigues Moraes, Lia Mesquita Lousada Quintão, Luciana Ribeiro Montenegro, Maria Teresa Martins Ferrari, Alexander A Jorge, Ivo J P Arnhold, Elaine Maria Frade Costa, Sorahia Domenice, Berenice Bilharinho Mendonca
Publikováno v:
The Journal of clinical endocrinology and metabolism. 107(5)
Context Massively parallel sequencing (MPS) technologies have emerged as a first-tier approach for diagnosing several pediatric genetic syndromes. However, MPS has not been systematically integrated into the diagnostic workflow along with clinical/bi
Autor:
Juliana Moreira Silva, Amanda de Moraes Narcizo, Anna Flavia Figueredo Benedetti, Alexander A. L. Jorge, Luciani R. Carvalho, Nathalia Garcia Bianchi Pereira Ferreira, Ivo J.P. Arnhold, Qing Fang, Mariana Cotarelli Madi, Mirian Yumie Nishi, Berenice B. Mendonca, Marilena Nakaguma, Ayse Bilge Ozel, Luciana Ribeiro Montenegro, Lais Cavalca Cardoso, Mariana F A Funari, Sally A. Camper, Jun Li, Qianyi Ma
Publikováno v:
Genes
Volume 12
Issue 8
Genes, Vol 12, Iss 1128, p 1128 (2021)
Volume 12
Issue 8
Genes, Vol 12, Iss 1128, p 1128 (2021)
We report four allelic variants (three novel) in three genes previously established as causal for hypopituitarism or related disorders. A novel homozygous variant in the growth hormone gene, GH1 c.171delT (p.Phe 57Leufs*43), was found in a male patie
Autor:
Ana Claudia Latronico, Alexander A. L. Jorge, Luciana Ribeiro Montenegro, Lorena Guimaraes Lima Amato, Leticia Ferreira Gontijo Silveira, Berenice B. Mendonca, Priscila Sales Barroso, Gabriela A Vasques, Antonio M. Lerario
Publikováno v:
Neuroendocrinology. 110(11-12)
Introduction: Constitutional delay of growth and puberty (CDGP) is the most prevalent cause of delayed puberty in both sexes. Family history of delayed puberty (2 or more affected members in a family) has been evidenced in 50–75% of patients with C
Autor:
Ana Paula Abreu, David Haig, Melissa Andrew, Dakota C. Jacobs, Berenice B. Mendonca, Andrew Dauber, Matthew T. Weirauch, Rona S. Carroll, Ana Claudia Latronico, Delanie B. Macedo, Patrick E. Chappell, Marina Cunha-Silva, Stephanie A. Roberts, Ursula B. Kaiser, Guillaume Labilloy, Danielle S Bessa, Luciana Ribeiro Montenegro, Vinicius Nahime Brito, Andrew Kirby
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Context:Central precocious puberty (CPP) results from premature activation of the hypothalamic–pituitary–gonadal axis. Few genetic causes of CPP have been identified, with the most common being mutations in the paternally expressed imprinted gene