Zobrazeno 1 - 10 of 19 pro vyhledávání: '"Lívia Maris Ribeiro Paranaíba"'
1
Akademický článek
Prevalence of depressive symptoms in patients with cleft lip and palate
Autor: Leonardo Santos Lima, Gustavo Silveira Ribeiro, Sibele Nascimento de Aquino, Fernando Madalena Volpe, Daniella Reis Barbosa Martelli, Mário Sérgio Oliveira Swerts, Lívia Maris Ribeiro Paranaíba, Hercílio Martelli Júnior
Publikováno v: Brazilian Journal of Otorhinolaryngology, Vol 81, Iss 2, Pp 177-183 (2015)
INTRODUCTION: Cleft lip and/or palate (CL/P) represent the most common congenital anomalies of the face.OBJECTIVE: To evaluate the prevalence of depressive symptoms in children and adolescents with nonsyndromic cleft lip and/or palate (nsCL/P).METHOD
Externí odkaz: https://doaj.org/article/f29f491f0e1840f59dfa1bee3bac4094
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2
Akademický článek
Técnicas cirúrgicas correntes para fissuras lábio-palatinas, em Minas Gerais, Brasil Current surgical techniques for cleft lip-palate in Minas Gerais, Brazil
Autor: Lívia Maris Ribeiro Paranaíba, Hudson de Almeida, Letízia Monteiro de Barros, Daniella Reis Barbosa Martelli, Julian Dias Orsi Júnior, Hercílio Martelli Júnior
Publikováno v: Brazilian Journal of Otorhinolaryngology, Vol 75, Iss 6, Pp 839-843 (2009)
Fissuras do lábio e/ou palato (FL/P) representam as anomalias congênitas crânio-facial mais comuns. OBJETIVO: Avaliar as técnicas cirúrgicas correntes na reabilitação de FL/P em um Serviço de referência no Estado de Minas Gerais. MATERIAL E
Externí odkaz: https://doaj.org/article/34dc5f10b52b4577b60a2efc08e50ddf
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3
Two rare cases of oral metastasis arising from lung adenocarcinoma and esophageal carcinoma
Autor: Ciro-Dantas Dantas, Martinho-Campolina-Rebello Horta, Maria-Goretti-Freire de Carvalho, Lucianne-Maia-Costa Lima, Mário-Rodrigues de Melo-Filho, Breno Amaral Rocha, Lívia-Maris-Ribeiro Paranaíba, Giovanna-Ribeiro Souto
Publikováno v: Journal of Clinical and Experimental Dentistry
Rocha, Breno-Amaral ; Paranaíba, Lívia M. R. ; Dantas, Ciro-Dantas ; de Carvalho, Maria Goretti Freire ; Filho, Mário-Rodrigues-Melo ; Lima, Lucianne-Maia-Costa ; Souto, Giovanna Ribeiro ; Horta, Martinho Campolina Rebello. Two rare cases of oral metastasis arising from lung adenocarcinoma and esophageal carcinoma. En: Journal of Clinical and Experimental Dentistry, 12 10 2020: 999-1004
RODERIC. Repositorio Institucional de la Universitat de Valéncia
instname
RODERIC: Repositorio Institucional de la Universitat de Valéncia
Metastasis to the oral cavity are rare, representing only 1% of all oral malignancies, and originate from various sites such as the breast, prostate, lung and kidney. Clinically, they can simulate reactive and inflammatory lesions common in the oral
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1864137c07dc17fc90dd74e9c26ca4db
https://doi.org/10.4317/jced.57125
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5
Prevalence of depressive symptoms in patients with cleft lip and palate
Autor: Fernando Madalena Volpe, Gustavo Silveira Ribeiro, Mário Sérgio Oliveira Swerts, Sibele Nascimento de Aquino, Hercílio Martelli Júnior, Lívia Maris Ribeiro Paranaíba, Leonardo Santos Lima, Daniella Reis Barbosa Martelli
Publikováno v: Brazilian Journal of Otorhinolaryngology, Volume: 81, Issue: 2, Pages: 177-183, Published: APR 2015
Brazilian Journal of Otorhinolaryngology v.81 n.2 2015
Brazilian Journal of Otorhinolaryngology
Associação Brasileira de Otorrinolaringologia e Cirurgia Cérvico-Facial (ABORL-CCF)
instacron:ABORL-CCF
Brazilian Journal of Otorhinolaryngology, Vol 81, Iss 2, Pp 177-183 (2015)
INTRODUCTION: Cleft lip and/or palate (CL/P) represent the most common congenital anomalies of the face.OBJECTIVE: To evaluate the prevalence of depressive symptoms in children and adolescents with nonsyndromic cleft lip and/or palate (nsCL/P).METHOD
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b088b7ff7851fc52dd3ace8f28048e8b
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6
Síndrome de Waardenburg: aspectos oftalmológicos e critérios de diagnóstico: relatos de casos Waardenburg syndrome: ophthalmic findings and criteria for diagnosis: case reports
Autor: Luciano Sólia Nasser, Lívia Maris Ribeiro Paranaíba, Ana Cláudia Frota, Andreia Gomes, Gisele Versiani, Hercílio Martelli Júnior
Publikováno v: Arquivos Brasileiros de Oftalmologia, Vol 75, Iss 5, Pp 352-355 (2012)
OBJETIVO: Descrever as características clínicas e imaginológicas de duas famílias com a síndrome de Waardenburg, sendo uma do tipo I e outra do tipo II, enfatizando as manifestações oftalmológicas, bem como o padrão de herança genética. M
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doajarticles::a1466667ce3d6e5b0675d10be71f229b
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27492012000500012
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7
Akademický článek
Stress induced phosphoprotein 1 overexpression controls proliferation, migration and invasion and is associated with poor survival in oral squamous cell carcinoma
Autor: Mauricio Rocha Dourado, Amr Elseragy, Bruno Cesar da Costa, Fábio Haach Téo, Gustavo Narvaes Guimarães, Renato Assis Machado, Maija Risteli, Wafa Wahbi, Clarissa Araujo Gurgel Rocha, Lívia Máris Ribeiro Paranaíba, Wilfredo Alejandro González-Arriagada, Sabrina Daniela da Silva, Ana Lucia Carrinho Ayroza Rangel, Marcelo Rocha Marques, Carlos Rossa Junior, Tuula Salo, Ricardo D. Coletta
Publikováno v: Frontiers in Oncology, Vol 12 (2023)
ObjectiveAlthough there have been remarkable achievements in the molecular landscape of oral squamous cell carcinoma (OSCC) in recent years, bringing advances in the understanding of its pathogenesis, development and progression, little has been appl
Externí odkaz: https://doaj.org/article/c30439d8141d48e5829cdf7d53325583
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8
[Waardenburg syndrome--ophthalmic findings and criteria for diagnosis: case reports]
Autor: Luciano Sólia, Nasser, Lívia Maris Ribeiro, Paranaíba, Ana Cláudia, Frota, Andreia, Gomes, Gisele, Versiani, Hercílio, Martelli Júnior
Publikováno v: Arquivos brasileiros de oftalmologia. 75(5)
To describe the clinical and imaginological features of two families with Waardenburg syndrome: type I and II, with emphasis on ophthalmic manifestations, as well as the pattern of genetic inheritance.We conducted a clinical study involving two famil
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::148bd86171a63936a8ee1899ae1e1e34
https://pubmed.ncbi.nlm.nih.gov/23471332
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9
Apert syndrome: report of a case with emphasis on craniofacial and genetic features
Autor: Hercílio, Martelli, Lívia Maris Ribeiro, Paranaíba, Roseli Teixeira, de Miranda, Julian, Orsi, Ricardo D, Coletta
Publikováno v: Pediatric dentistry. 30(6)
Apert syndrome is 1 of the 5 craniosynostosis syndromes that shore clinical features and are caused by allelic mutations in the fibroblast growth factor receptor 2 (FGFR2) gene. The purpose of this paper was to report a case of Apert syndrome, with p
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::77d40a658c65e6a5540882c47ffb4dce
https://pubmed.ncbi.nlm.nih.gov/19186770
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