Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Roseli Teixeira, de Miranda"'
Autor:
Lívia Máris Ribeiro Paranaíba, Roseli Teixeira de Miranda, Leila Aparecida Ribeiro, Letízia Monteiro de Barros, Hercílio Martelli-Júnior
Publikováno v:
Revista Brasileira de Epidemiologia, Vol 14, Iss 1, Pp 151-160 (2011)
OBJECTIVE: To evaluate the frequency of craniofacial anomalies in patients treated at a Brazilian Reference Center for craniofacial deformities. METHOD: Retrospective epidemiological study evaluating the clinical records of 1,142 patients: 656 (57.4%
Externí odkaz:
https://doaj.org/article/61d6dd1b4e424ce98d154b5806112522
Autor:
Hercílio Martelli-Júnior, Roseli Teixeira de Miranda, Cassandro Moreira Fernandes, Paulo Rogério Ferreti Bonan, Lívia Máris Ribeiro Paranaíba, Edgard Graner, Ricardo D. Coletta
Publikováno v:
Journal of Applied Oral Science, Vol 18, Iss 6, Pp 646-649 (2010)
OBJECTIVES: Goldenhar syndrome (GS) is a relatively common developmental disorder characterized by craniofacial anomalies in association with vertebral, cardiac, renal, and central nervous system defects. This paper describes GS features with special
Externí odkaz:
https://doaj.org/article/7b0a36836e0148edaf90852aff1dc3e0
Autor:
Lívia Máris Ribeiro Paranaíba, Roseli Teixeira de Miranda, Daniella Reis Barbosa Martelli, Paulo Rogério Ferreti Bonan, Hudson de Almeida, Julian Miranda Orsi Júnior, Hercílio Martelli Júnior
Publikováno v:
Brazilian Journal of Otorhinolaryngology, Vol 76, Iss 5, Pp 649-653 (2010)
Fissuras do lábio e/ou palato (FL/P) representam as anomalias congênitas mais comuns da face, correspondendo a aproximadamente 65% de todas as malformações da região craniofacial. OBJETIVO: Descrever casos clínicos incomuns de FL/P não-sindrô
Externí odkaz:
https://doaj.org/article/8f6774c53d9140c4ad8bc67c31f95ada
Autor:
Florence J. M. Cuadra‐Zelaya, Ricardo D. Coletta, Renato Corrêa Viana Casarin, Renato Assis Machado, Hercílio Martelli-Júnior, Mônica Grazieli Corrêa, Roseli Teixeira de Miranda, Francisco Humberto Nociti
Publikováno v:
American Journal of Medical Genetics Part A. 179:2124-2131
Papillon-Lefevre syndrome (PLS; MIM#245000) is a rare recessive autosomal disorder characterized by palmar and plantar hyperkeratosis, and aggressively progressing periodontitis leading to premature loss of deciduous and permanent teeth. PLS is cause
Autor:
Sarah Vitor Teixeira Rodrigues, Maria Carolina Vaz Goulart, Fernanda Barbosa Esteves Rocha, Caroline Maria De Souza, Roseli Teixeira de Miranda, Mirella Moreira Miguel, Gérsika Bitencourt Santos
Publikováno v:
Revista Eletrônica Acervo Odontológico. 3:e5893
Paracoccidioidomycosis is a fungal disease resulting from the dimorphic fungus Paracoccidioides brasiliensis that has a predilection for hot and humid places, which is why there is a high incidence of the disease in Brazil. The primary site of the di
Reflexões sobre o tratamento da informação na Documentação Jurídica, com base na tríade: leitura documentária, linguagem jurídica e análise de discurso. Nesse contexto, discutem-se terminologia e representação da informação, em função
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6efe4944c9bd3efb7dba12fc340b7093
Autor:
Ricardo D. Coletta, Lívia Máris Ribeiro Paranaíba, Cassandro Moreira Fernandes, Paulo Rogério Ferreti Bonan, Hercílio Martelli-Júnior, Edgard Graner, Roseli Teixeira de Miranda
Publikováno v:
Journal of Applied Oral Science, Vol 18, Iss 6, Pp 646-649 (2010)
Journal of Applied Oral Science, Volume: 18, Issue: 6, Pages: 646-649, Published: DEC 2010
Journal of Applied Oral Science
Journal of Applied Oral Science v.18 n.6 2010
Journal of applied oral science
Universidade de São Paulo (USP)
instacron:USP
Journal of Applied Oral Science, Volume: 18, Issue: 6, Pages: 646-649, Published: DEC 2010
Journal of Applied Oral Science
Journal of Applied Oral Science v.18 n.6 2010
Journal of applied oral science
Universidade de São Paulo (USP)
instacron:USP
OBJECTIVES: Goldenhar syndrome (GS) is a relatively common developmental disorder characterized by craniofacial anomalies in association with vertebral, cardiac, renal, and central nervous system defects. This paper describes GS features with special
Autor:
Roseli Teixeira de Miranda, Luís Antônio Nogueira dos Santos, Hercílio Martelli, Paulo Rogério Ferreti Bonan, Letízia Monteiro de Barros
Publikováno v:
Journal of Oral Science. 52:509-512
Hemifacial hyperplasia is a developmental disorder characterized by marked unilateral facial asymmetry. It involves the hard and soft tissues of the face. The cause is unknown, although several predisposing factors have been described. A case report
Autor:
Hudson de Almeida, Lívia Máris Ribeiro Paranaíba, Roseli Teixeira de Miranda, Daniella Reis Barbosa Martelli, Paulo Rogério Ferreti Bonan, Hercílio Martelli Júnior, Julian Miranda Orsi Júnior
Publikováno v:
Brazilian Journal of Otorhinolaryngology, Volume: 76, Issue: 5, Pages: 649-653, Published: OCT 2010
Brazilian Journal of Otorhinolaryngology v.76 n.5 2010
Brazilian Journal of Otorhinolaryngology
Associação Brasileira de Otorrinolaringologia e Cirurgia Cérvico-Facial (ABORL-CCF)
instacron:ABORL-CCF
Brazilian Journal of Otorhinolaryngology v.76 n.5 2010
Brazilian Journal of Otorhinolaryngology
Associação Brasileira de Otorrinolaringologia e Cirurgia Cérvico-Facial (ABORL-CCF)
instacron:ABORL-CCF
Fissuras do lábio e/ou palato (FL/P) representam as anomalias congênitas mais comuns da face, correspondendo a aproximadamente 65% de todas as malformações da região craniofacial. OBJETIVO: Descrever casos clínicos incomuns de FL/P não-sindrô
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60ede33f5052386220741a83843a2f5d
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1808-86942010000500019&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1808-86942010000500019&lng=en&tlng=en
Autor:
Roseli Teixeira de Miranda, Hercílio Martelli-Júnior, Lívia Máris Ribeiro Paranaíba, Ruy Camargo Abdo Filho, Andreia Bufalino, Ricardo D. Coletta
Publikováno v:
The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association. 47(5)
Ectrodactyly-ectodermal dysplasia-clefting syndrome is an uncommon disorder that includes a clinical spectrum of limb, facial, ocular, internal ear, and urogenital malformations. The disease is caused by heterozygous mutations in the 3q27–29 locate