Resultados de procura - Priscila Gagliardi
- Mostrando 1 - 8 Resultados de 8
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1
Randomized Trial of Aromatase Inhibitors, Growth Hormone, or Combination in Pubertal Boys with Idiopathic, Short Stature por Nelly Mauras, Judith L. Ross, Priscila Gagliardi, Yamaguchi Yu, Jobayer Hossain, Joseph Permuy, Ligeia Damaso, Debbie Merinbaum, Ravinder J. Singh, Ximena Gaete, Verónica Mericq
Publicado 2016Artigo -
2
SUN-264 Mutations in the Maternally Imprinted Genes, MKRN3 and DLK1, Associated with Central Precocious Puberty por Ana Paula Abreu, Leonardo Garcia, Sidney Alcântara Pereira, Delanie B. Macedo, Melissa Magnusson, Priscila Gagliardi, Filiz Tütüncüler, Keisha Bird, Adriana Lofrano‐Porto, Stephanie Roberts, Rona S. Carroll, Ana Cláudia Latronico, Ursula B. Kaiser
Publicado 2019Artigo -
3
MON-251 Clinical Features of a Large Cohort of Patients with Familial Central Precocious Puberty Caused by Loss-of-Function Mutations in MKRN3 por Carlos Eduardo Seraphim, Ana Pinheiro Machado Canton, Luciana Ribeiro Montenegro, Maiara Ribeiro Piovesan, Marina Cunha-Silva, Delanie B. Macedo, Aline Guimarães, Carolina Ramos, Priscila Gagliardi, Ana Paula Abreu, Ursula B. Kaiser, Berenice B. Mendonça, Vinícius Nahime Brito, Ana Cláudia Latronico
Publicado 2019Artigo -
4
Novel <i>MKRN3</i> Missense Mutations Associated With Central Precocious Puberty Reveal Distinct Effects on Ubiquitination por John C Magnotto, Alessandra Mancini, Keisha Bird, Luciana Ribeiro Montenegro, Filiz Tütüncüler, Sidney Alcântara Pereira, Vitoria Simas, Leonardo Garcia, Stephanie Roberts, Delanie B. Macedo, Melissa Magnuson, Priscila Gagliardi, Nelly Mauras, Selma F. Witchel, Rona S. Carroll, Ana Cláudia Latronico, Ursula B. Kaiser, Ana Paula Abreu
Publicado 2023Artigo -
5
Central Precocious Puberty Caused by Mutations in the Imprinted Gene <i>MKRN3</i> por Ana Paula Abreu, Andrew Dauber, Delanie B. Macedo, Sekoni D. Noel, Vinícius Nahime Brito, John C. Gill, Priscilla Cukier, Iain Thompson, Víctor M. Navarro, Priscila Gagliardi, Tânia Maria Barreto Rodrigues, Cristiane Kochi, Carlos Alberto Longui, Dominique Beckers, Francis de Zegher, Luciana Ribeiro Montenegro, Berenice B. Mendonça, Rona S. Carroll, Joel N. Hirschhorn, Ana Cláudia Latronico, Ursula B. Kaiser
Publicado 2013Artigo -
6
CLCN2 chloride channel mutations in familial hyperaldosteronism type II por Ute I. Scholl, Gabriel Stölting, Julia Schewe, Anne Thiel, Hua Tan, Carol Nelson‐Williams, Alfred A. Vichot, Sheng Chih Jin, Erin Loring, Verena Untiet, Taekyeong Yoo, Jungmin Choi, Shengxin Xu, Wu A, Marieluise Kirchner, Philipp Mertins, Lars Christian Rump, Ali Mirza Onder, Cory Gamble, Daniel W. McKenney, Robert W. Lash, Deborah P. Jones, G. Chune, Priscila Gagliardi, Murim Choi, Richard D. Gordon, Michael Stowasser, Christoph Fahlke, Richard P. Lifton
Publicado 2018Carta -
7
SUN-085 Clinical and Hormonal Features of 37 Families with Central Precocious Puberty Due to MKRN3 Loss-Of -Function Mutations por Carlos Eduardo Seraphim, Ana Pinheiro Machado Canton, Luciana Ribeiro Montenegro, Maiara Ribeiro Piovesan, Tabata Mariz Bohlen, Renata Frazão, Delanie B. Macedo, Aline Guimarães de Faria, Carolina Ramos, Priscila Gagliardi, Ana Paula Abreu, Andréa de Castro Leal, Margaret de Castro, Sonir Roberto Rauber Antonini, Leandro Soriano‐Guillén, Arancha Escribano-Muñoz, Raquel Corripio, José Ignacio Labarta, Lourdes Travieso‐Suárez, Nelmar Valentina Ortiz‐Cabrera, Jesús Argente, Berenice B. Mendonça, Ursula B. Kaiser, Vinícius Nahime Brito, Ana Cláudia Latronico
Publicado 2020Artigo -
8
Genotype–Phenotype Correlations in Central Precocious Puberty Caused by <i>MKRN3</i> Mutations por Carlos Eduardo Seraphim, Ana Pinheiro Machado Canton, Luciana Ribeiro Montenegro, Maiara Ribeiro Piovesan, Delanie B. Macedo, Marina Cunha, Aline Guimarães, Carolina Ramos, Anna Flavia Figueiredo Benedetti, Andréa de Castro Leal, Priscila Gagliardi, Sonir Roberto Rauber Antonini, Mirta Gryngarten, Andrea Arcari, Ana Paula Abreu, Ursula B. Kaiser, Leandro Soriano‐Guillén, Arancha Escribano-Muñoz, Raquel Corripio, José Ignacio Labarta, Lourdes Travieso‐Suárez, Nelmar Valentina Ortiz‐Cabrera, Jesús Argente, Berenice B. Mendonça, Vinícius Nahime Brito, Ana Cláudia Latronico
Publicado 2020Artigo
Ferramentas de procura:
Materias Relacionadas
Biology
Endocrinology
Gene
Genetics
Hormone
Internal medicine
Medicine
Mutation
Missense mutation
Precocious puberty
Frameshift mutation
Cohort
Bone age
Context (archaeology)
DNA methylation
Gene expression
Genomic imprinting
Nonsense mutation
Paleontology
Pediatrics
Sanger sequencing
Adrenarche
Aldosterone
Anthropometry
Aromatase
Biochemistry
Breast cancer
Breast development
Cancer
Central precocious puberty