Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Isabella L, Monlleó"'
Autor:
Elaine Lustosa-Mendes, Ana P. dos Santos, Társis P. Vieira, Erlane M. Ribeiro, Adriana A. Rezende, Agnes C. Fett-Conte, Denise P. Cavalcanti, Têmis M. Félix, Isabella L. Monlleó, Vera Lúcia Gil-da-Silva-Lopes
Publikováno v:
Jornal de Pediatria, Vol 97, Iss 3, Pp 321-328 (2021)
Objective: This article presents a clinical and cytogenomic approach that focuses on the diagnosis of syndromic oral clefts (OCs). Methods: The inclusion criteria were individuals with OC presenting four or more minor signs and no major defects (non-
Externí odkaz:
https://doaj.org/article/d7933406576f4f5abfff7f3417dc9625
Autor:
Isabella L. Monlleó, Amanda G.R. de Barros, Marshall I.B. Fontes, Ana K.M. de Andrade, Gisele de M. Brito, Diogo L.L. do Nascimento, Vera L. Gil-da-Silva-Lopes
Publikováno v:
Jornal de Pediatria, Vol 91, Iss 5, Pp 485-492 (2015)
ABSTRACT OBJECTIVES: To describe prevalence of associated defects and clinical-genetic characteristics of patients with typical orofacial clefts seen at a reference genetic service. METHODS: Descriptive study conducted between September of 2009 and J
Externí odkaz:
https://doaj.org/article/4bce68be85854ea28a871579709d752e
Autor:
Samira Spineli-Silva, Isabella L. Monlleó, Têmis M. Félix, Vera L. Gil-da-Silva-Lopes, Társis P. Vieira
Publikováno v:
The Cleft Palate Craniofacial Journal. :105566562311744
This study reports three patients with Cat-eye Syndrome (CES), two of which present a previous clinical diagnosis of Craniofacial microsomia (CFM). Chromosomal microarray analysis (CMA) revealed a tetrasomy of 1,7 Mb at the 22q11.2q11.21 region, whic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ca15d760e3f534d22f90f3705849c1ef
https://doi.org/10.1177/10556656231174435
https://doi.org/10.1177/10556656231174435
Autor:
Isabella L. Monlleó, Susane V. Zanotti, Bárbara Priscila B. de Araújo, Erisvaldo F. Cavalcante Júnior, Paula D. Pereira, Paulo M. de Barros, Maria Deysiane P. Araújo, Ana Thaysa V. S. de Mendonça, Catarina R. S. Santos, Ylana R. dos Santos, Débora de Paula Michelatto, Maricilda P. de Mello, Andrea T. Maciel-Guerra, Gil Guerra-Júnior
Publikováno v:
Jornal de Pediatria, Vol 88, Iss 6, Pp 489-495 (2012)
OBJETIVOS: Avaliar a prevalência e descrever alterações da morfologia genital em recém-nascidos em duas maternidades-escola de gestão pública. MÉTODOS: Estudo caso/controle, descritivo, transversal. Utilizou-se protocolo clínico para avaliaç
Externí odkaz:
https://doaj.org/article/718fcbb8efbb4847bdbb78450bf27952
Autor:
Roberta M, Volpe-Aquino, Isabella L, Monlleó, Elaine, Lustosa-Mendes, Amanda F, Mora, Agnes C, Fett-Conte, Têmis M, Félix, Ana C, Xavier, Rita, Tonocchi, Erlane M, Ribeiro, Rui, Pereira, Raquel T, Boy da Silva, Adriana A, de Rezende, Denise P, Cavalcanti, Vera L, Gil-da-Silva-Lopes
Publikováno v:
Birth defects research. 110(1)
The World Health Organization has recognized the relevance of databases on craniofacial anomalies since . To date, there is no universal standard instrument/database focused on risk factors, clinical and genetic data collection, and follow-up that en
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::37b5ffce80fd2bbdef7348174d2e98e2
https://pubmed.ncbi.nlm.nih.gov/28949457
https://pubmed.ncbi.nlm.nih.gov/28949457