Výsledky vyhledávání - "Luciano Sólia-Nasser"

Akademický článek

Prevalência de Tracoma em crianças em idade escolar no município de Turmalina, MG

Autor: Evanildo José da Silva, Layze Alves Vieira Oliveira, Luciano Sólia Nasser, Luciana Fernandes Amaro Leite, Antônio Prates Caldeira, Leida Calegário de Oliveira

Publikováno v: Revista Brasileira de Oftalmologia, Vol 75, Iss 3, Pp 181-184 (2016)

RESUMO O tracoma, tido equivocadamente como erradicado em nosso meio, encontra-se na lista de doenças negligenciadas. Trata-se da maior causa de cegueira evitável do mundo, sendo encontrado predominantemente nos países subdesenvolvidos. Diversos t

Externí odkaz: https://doaj.org/article/7453e9fc9ac7472ababc4edcfe8de13d

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Akademický článek

Association between hypertelorism and nonsyndromic oral clefts

Autor: Luciano Sólia Nasser, Letízia Monteiro de Barros, Daniella Reis Barbosa Martelli, João Vitor Quadros Tonelli, Mário Sérgio Oliveira Swerts, Hercílio Martelli Júnior

Publikováno v: Brazilian Journal of Oral Sciences, Vol 17 (2018)

Hypertelorism is characterized by the increased distance between the orbits, measured from the most medial portion of its inner walls. It represents a signal found in sev eral craniofacial defects, and oral clefts. Nonsyndromic oral clefts (NOC) are

Externí odkaz: https://doaj.org/article/572109b044b5467b85b2f7140543f6b4

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Report of two unrelated families with Jalili syndrome and a novel nonsense heterozygous mutation in CNNM4 gene

Autor: Renato Assis Machado, Hercílio Martelli-Júnior, Priscila Hae Hyun Rim, Ricardo D. Coletta, Elaine Lustosa-Mendes, Luciano Sólia Nasser, Vera Lúcia Gil-da-Silva-Lopes, Célia Márcia Fernandes Maia, Daniella Reis Barbosa Martelli, Verônica Oliveira Dias

Publikováno v: European Journal of Medical Genetics. 61:384-387

Jalili syndrome (JS) is an autosomal recessive disease characterized by a combination of cone-rode retinal dytrophy (CRD) and amelogenesis imperfect (AI). Mutations in cyclin and CBS domain divalent metal cation transport mediator 4 (CNNM4) gene caus

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee2b282471a327bec71fb2a831c85cae
https://doi.org/10.1016/j.ejmg.2018.02.003

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Waardenburg syndrome type I: dental phenotypes and genetic analysis of an extended family

Autor: Luciano Sólia-Nasser, Hercílio Martelli-Júnior, Aline-Francoise Cardoso, Pedro dos-Santos-Neto, Andreia Gomes, Sibele-Nascimento de Aquino, Lívia-Maris-R. Paranaíba, R. D. Coletta, Ana-Cláudia Frota

Publikováno v: Solia-Nasser, Luciano ; Aquino, Sibele Nascimento de ; Paranaíba, Lívia M. R. ; Gomes, Andreia ; Santos Neto, Pedro Eleutério dos ; Della Coletta, Ricardo ; Cardoso, Aline-Francoise ; Frota, Ana-Cláudia ; Martelli Júnior, Hercílio. Waardenburg syndrome type I: dental phenotypes and genetic analysis of an extended family. En: Medicina oral, patología oral y cirugía bucal. Ed inglesa, 2016, Vol. 21, No. 3: 321
RODERIC. Repositorio Institucional de la Universitat de Valéncia
instname
Medicina Oral, Patología Oral y Cirugía Bucal

Background: The aim of this study was to describe the pattern of inheritance and the clinical features in a large family with Waardenburg syndrome type I (WS1), detailing the dental abnormalities and screening for PAX3 mutations. Material and Methods

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c3b3e63a58edf1cfc1304936728463f
http://hdl.handle.net/10550/54775

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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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OP - AMELOGENESIS IMPERFECTA AND JALILI SYNDROME: A CASE REPORT

Autor: Verônica Oliveira Dias, Hercílio Martelli, Daniella R. Barbosa Martelli, Célia Fenandes Maia, Luciano Sólia Nasser, Ricardo D. Coletta

Publikováno v: Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology. 123:e33

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::79015848c568051e5731b7cd2480a7ed
https://doi.org/10.1016/j.oooo.2016.09.013

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Oclusão da artéria central da retina secundária a cineangiocoronariografia via artéria braquial: relato de caso Central retinal artery occlusion secondary to brachial cineangiocoronography: case report

Autor: Augusto Nakashima, Alan Diego Negretto, Alexandre Antonio Marques Rosa, Yoshitaka Nakashima, Luciano Sólia Nasser

Publikováno v: Arquivos Brasileiros de Oftalmologia, Vol 70, Iss 5, Pp 851-853 (2007)

Os autores relatam o caso de um paciente com insuficiência coronariana que desenvolveu quadro de oclusão de artéria central da retina após ser submetido a cateterização cardíaca por via braquial e realização de cineangiocoronariografia. Este

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doajarticles::f837e2028d9e103869b72c3cc6809e4d
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27492007000500022

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[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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[Central retinal artery occlusion secondary to brachial cineangiocoronography: case report]

Autor: Augusto, Nakashima, Alan Diego, Negretto, Alexandre Antonio Marques, Rosa, Yoshitaka, Nakashima, Luciano Sólia, Nasser

Publikováno v: Arquivos brasileiros de oftalmologia. 70(5)

The authors report a case of a patient with coronary insufficiency who developed central retinal artery occlusion following cardiac catheterism through the brachial artery and cineangiocoronography. This procedure can lead to embolic phenomena like t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::0548a5ca06c7c2531688cf2826c98791
https://pubmed.ncbi.nlm.nih.gov/18157313

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