Results 81 to 90 of about 291 (104)

SINDROME DE HORNER, UMA RARA COMPLICAÇAO POS-OPERATORIA DE PARATIREOIDECTOMIA E TIREOIDECTOMIA SUBTOTAL: RELATO DE CASO

BJN Abstract-CPN25
Introdução: A síndrome de claude bernard-horner é uma condição neurológica que ocorre devido à interrupção da via simpática que conecta o hipotálamo ao olho, composta por três neurônios.
Edna Carla Epifânio, Giselle Reis Fernandes, M. Silva, Suellen Christina Klein, Edgard Augusto Villas Boas   +4 more
semanticscholar   +1 more source

COMPARAÇÃO DOS DESFECHOS CARDIOMETABÓLICOS ENTRE AGONISTAS DE GLP-1 E CIRURGIA BARIÁTRICA EM PACIENTES COM SÍNDROME METABÓLICA

Lumen et Virtus
Metabolic syndrome is a set of interrelated metabolic disorders, including abdominal obesity, dyslipidemia, arterial hypertension and insulin resistance, which significantly increase the risk of cardiovascular disease and type 2 diabetes.
Francisco de Oliveira Borges, Victor Rocha Dias, Mateus Giovani Senna, Laura de Paiva Rodrigues da Silva, Shanna Silva Mello Dantas, Thaís Gomes De Oliveira, Marines Valadares Freitas De Castro, Valdinei Klein Conti, Lia Amaral de Sousa, Diegomaier Nunes Neri, Fabio Shiavon, Jaime Javier Garcia Caro, Larissa Gabriele Fausto Silva, Gillyane Pedreira Silva, Lucas Cardeal Simão Ribeiro   +14 more
semanticscholar   +1 more source

Biallelic variants in PAX3 cause Klein syndrome

Clinical Genetics, 2022
Joël Zlotogora
exaly  

Síndrome de implantación del cemento

, 2016
M. Morozov, B. Klein
semanticscholar   +1 more source

Alterações dentárias na síndrome de waardenburg

, 2014
Edimilson Martins de Freitas, Aquino Sn, Paranaíba Lmr, R. D. Coletta, H. MartelliJúnior   +4 more
semanticscholar   +1 more source

Waardenburg syndrome type 3 (Klein-Waardenburg syndrome) segregating with a heterozygous deletion in the paired box domain ofPAX3: a simple variant or a true syndrome?

Clinical Genetics, 2001
Mustafa Tekin
exaly  

O SUJEITO COM A SÍNDROME DE WAARDENBURG NA ESCOLA COMUM: UM ESTUDO DE CASO

, 2014
Fabiana Zanol Araújo, M. Araújo, V. M. Gonring   +2 more
semanticscholar   +1 more source

Autosomal dominant inheritance of Klein-Waardenburg syndrome

American Journal of Medical Genetics Part A, 1992
Joël Zlotogora
exaly  

First report of Klein-Waardenburg Syndrome in Iran and a novel pathogenic splice site variant in PAX3 gene

International Journal of Pediatric Otorhinolaryngology, 2018
Hamzeh Salmani, Arezou Karamzade, Mohammad Keramatipour   +2 more
exaly  

Homozygous and heterozygous inheritance of PAX3 mutations causes different types of Waardenburg syndrome

American Journal of Medical Genetics, Part A, 2003
Hulya Kayserili
exaly