Zobrazeno 1 - 10
of 116
pro vyhledávání: '"Iêda M, Orioli"'
Autor:
Ronilo Ragodos, Tong Wang, Carmencita Padilla, Jacqueline T. Hecht, Fernando A. Poletta, Iêda M. Orioli, Carmen J. Buxó, Azeez Butali, Consuelo Valencia-Ramirez, Claudia Restrepo Muñeton, George L. Wehby, Seth M. Weinberg, Mary L. Marazita, Lina M. Moreno Uribe, Brian J. Howe
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-8 (2022)
Abstract Children with orofacial clefting (OFC) present with a wide range of dental anomalies. Identifying these anomalies is vital to understand their etiology and to discern the complex phenotypic spectrum of OFC. Such anomalies are currently ident
Externí odkaz:
https://doaj.org/article/3800fcecdedd481ebcf9fe8c511f1042
Autor:
Helen Dolk, Boris Groisman, Joan Morris, Rosa Pardo, Elizabeth Limb, Iêda M Orioli, Adriana Benavides-Lara, María de la Paz Barboza-Arguello, Maria Aurora Canessa Tapia, Giovanny Vinícius Araújo de França, Jorge Holguin, Paula Margarita Hurtado-Villa, Marisol Ibarra Ramirez, Cecilia Mellado, Dania Maria Pastora Bucardo, Catherin Rodríguez, Ignacio Zarante
Publikováno v:
BMJ Paediatrics Open, Vol 5, Iss 1 (2021)
Objective The Latin American Network of Congenital Malformations: ReLAMC was established in 2017 to provide accurate congenital anomaly surveillance. This study used data from ReLAMC registries to quantify the prevalence of microcephaly from 2010 to
Externí odkaz:
https://doaj.org/article/5b0400fc4d8a4c33a2ef2fc7f22012d7
Autor:
Ronilo Ragodos, Tong Wang, Carmencita Padilla, Jacqueline T. Hecht, Fernando A. Poletta, Iêda M. Orioli, Carmen J. Buxó, Azeez Butali, Consuelo Valencia-Ramirez, Claudia Restrepo Muñeton, George L. Wehby, Seth M. Weinberg, Mary L. Marazita, Lina M. Moreno Uribe, Brian J. Howe
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-1 (2022)
Externí odkaz:
https://doaj.org/article/63f57458558b42f78b2802c5a0743553
Autor:
Brian J. Howe, Chandler Pendleton, Miyuraj Harishchandra Hikkaduwa Withanage, Christopher A. Childs, Erliang Zeng, Arjen van Wijk, Ruurd Hermus, Carmencita Padilla, Jacqueline T. Hecht, Fernando A. Poletta, Iêda M. Orioli, Carmen J. Buxó-Martínez, Frederic Deleyiannis, Alexandre R. Vieira, Azeez Butali, Consuelo Valencia-Ramirez, Claudia Restrepo Muñeton, George L. Wehby, Seth M. Weinberg, Mary L. Marazita, Lina M. Moreno Uribe, Xian-Jin Xie
Publikováno v:
Dentistry Journal, Vol 10, Iss 7, p 128 (2022)
Individuals with orofacial clefting (OFC) have a higher prevalence of tooth agenesis (TA) overall. Neither the precise etiology of TA, nor whether TA occurs in patterns that differ by gender or cleft type is yet known. This meta-analysis aims to iden
Externí odkaz:
https://doaj.org/article/91b389eb162e410caba2b94f455fc1fd
Autor:
Katherine Neiswanger, Nandita Mukhopadhyay, Shwetha Rajagopalan, Elizabeth J Leslie, Carla A Sanchez, Jacqueline T Hecht, Iêda M Orioli, Fernando A Poletta, Javier Enríquez de Salamanca, Seth M Weinberg, Mary L Marazita
Publikováno v:
PLoS ONE, Vol 15, Iss 3, p e0230534 (2020)
Dermatoglyphic patterns on the fingers often differ in syndromes and other conditions with a developmental component, compared to the general population. Previous literature on the relationship between orofacial clefts-the most common craniofacial bi
Externí odkaz:
https://doaj.org/article/dd806ce1c31549b188c19881c86818ad
Autor:
Joissy Aprigio, Carolina M. L. de Castro, Marcelo A. Costa Lima, Márcia G. Ribeiro, Iêda M. Orioli, Márcia R. Amorim
Publikováno v:
J Community Genet
Down syndrome is the main genetic cause of intellectual disability. Many studies describe the clinical characteristics of DS patients; however, few have investigated the clinical profile of mothers who have children with DS. Advanced maternal age (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a403ad9135987d9b3b30b653aef287a3
https://europepmc.org/articles/PMC10104982/
https://europepmc.org/articles/PMC10104982/
Autor:
Ana Maria Bolognese, Milagros M. Duenas-Roque, Viviane Freitas de Castro, Maria Teresa Vieira Sanseverino, Viviana Cosentino, Rachel Sayuri Honjo, Larissa Souza Mario Bueno, Juan C. Llerena, Luiz Carlos Santana da Silva, Júlio César Loguercio Leite, Daniel Mattos, Márcia Pereira Alves de Souza, Denise P. Cavalcanti, Pablo Barbero, Pricila Bernardi, Flávia Martinez de Carvalho, Patrícia Santana Correia, Clarice Pagani Savastano, Iêda M. Orioli
Publikováno v:
Molecular Syndromology. 12:219-233
Holoprosencephaly (HPE) is the failure of the embryonic forebrain to develop into 2 hemispheres promoting midline cerebral and facial defects. The wide phenotypic variability and causal heterogeneity make genetic counseling difficult. Heterozygous va
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ba2f0476a84a943b99e0e9ec2a83f4e
https://doi.org/10.1159/000515044
https://doi.org/10.1159/000515044
Autor:
Lucas Gabriel Gimenez, Marta Ascurra, Paula Hurtado-Villa, Jorge S. Lopez-Camelo, Maria Aurora Canessa‐Tapia, Dania Maria Pastora, Flávia Martinez de Carvalho, Daniel Mattos Correa, Iêda M. Orioli, Adriana Benavides-Lara, Boris Groisman, Flávia Schneider Soares, Giovanny Vinícius Araújo de França, Marisol Ibarra-Ramírez, Mariana Piola, Rosa Pardo, Helen Dolk, Ignacio Zarante, Eliana de Aquino Bonilha
Publikováno v:
American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 184:1078-1091
The early detection of congenital anomaly epidemics occurs when comparing current with previous frequencies in the same population. The success of epidemiologic surveillance depends on numerous factors, including the accuracy of the rates available i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26b277a7c232a409c943ffd94f340b68
https://doi.org/10.1002/ajmg.c.31872
https://doi.org/10.1002/ajmg.c.31872
Autor:
Jacqueline T. Hecht, Carmencita D. Padilla, Lina M. Moreno Uribe, Consuelo Valencia-Ramirez, Tong Wang, Iêda M. Orioli, Seth M. Weinberg, Carmen J. Buxó, Azeez Butali, Fernando A. Poletta, B.J. Howe, George L. Wehby, Mary L. Marazita, Ronilo Ragodos, Claudia P. Restrepo Muñeton
Children with orofacial clefting (OFC) present with a wide range of dental anomalies. Identifying these anomalies is vital to understand their etiology and to discern the complex phenotypic spectrum of OFC. Such anomalies are currently identified usi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c64bb247e93ba4ba06b4aac6d67cb7b
https://doi.org/10.21203/rs.3.rs-1061414/v1
https://doi.org/10.21203/rs.3.rs-1061414/v1
Autor:
Ronilo, Ragodos, Tong, Wang, Carmencita, Padilla, Jacqueline T, Hecht, Fernando A, Poletta, Iêda M, Orioli, Carmen J, Buxó, Azeez, Butali, Consuelo, Valencia-Ramirez, Claudia, Restrepo Muñeton, George L, Wehby, Seth M, Weinberg, Mary L, Marazita, Lina M, Moreno Uribe, Brian J, Howe
Publikováno v:
Scientific reports. 12(1)
Children with orofacial clefting (OFC) present with a wide range of dental anomalies. Identifying these anomalies is vital to understand their etiology and to discern the complex phenotypic spectrum of OFC. Such anomalies are currently identified usi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2347a494bbe78520691be3a4f7f924f4
https://pubmed.ncbi.nlm.nih.gov/35941160
https://pubmed.ncbi.nlm.nih.gov/35941160