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Hallazgos anatomohistopatológicos en un canino con enfermedad glomerular quística bilateralAnatomohistopathological findings in a dog with bilateral glomerular cystic disease
(Universidad Nacional del Nordeste. Facultad de Ciencias VeterinariasRevista Veterinaria, 2007-01-01)
El objetivo de esta comunicación fue reportar los hallazgos anatomohistopatológicos de un caso de enfermedad glomerular quística bilateral en un cachorro de cuatro meses de edad, de raza pastor alemán, que concurrió a la ...
Idiopathic pulmonary hemosiderosis with cystic lesions: A rare presentation
(Lippincott Williams & Wilkins, 2000-06-01)
This report describes a case of a 49-year-old man with cough, recurrent hemoptysis, and dyspnea during 18 months, presenting with radiological findings of alveolar infiltrate and cystic lesions in left upper lobe. Laboratory ...
Idiopathic pulmonary hemosiderosis with cystic lesions: A rare presentation
(Lippincott Williams & Wilkins, 2000-06-01)
This report describes a case of a 49-year-old man with cough, recurrent hemoptysis, and dyspnea during 18 months, presenting with radiological findings of alveolar infiltrate and cystic lesions in left upper lobe. Laboratory ...
Idiopathic pulmonary hemosiderosis with cystic lesions: A rare presentation
(2000-01-01)
This report describes a case of a 49-year-old man with cough, recurrent hemoptysis, and dyspnea during 18 months, presenting with radiological findings of alveolar infiltrate and cystic lesions in left upper lobe. Laboratory ...
Idiopathic pulmonary hemosiderosis with cystic lesions: A rare presentation
(Lippincott Williams & Wilkins, 2014)
Histogenesis of the cysts in the autosomal dominant polycystic kidney disease: An immunohistochemical study
(1998-01-01)
The histogenesis of the cysts in the autosomal dominant polycystic kidney disease was investigated in 33 patients by immunohistochemistry. The antibodies and lectins used to identify the different segments of the nephrons ...
Contribuição do exame de imagem para avaliação de pacientes com deficiência de alfa-galactosidase A
(Universidade Federal de São Paulo (UNIFESP), 2018-06-28)
Introduction: Alpha-galactosidase A (α-GalA) deficiency is more commonly referred
to as Fabry's disease. It is a rare, recessive, X-linked disease caused by mutations in
the gene encoding the lysosomalα-GalA enzyme, which ...
Variáveis clínicas e bioquímicas associadas com a evolução do peso e da estatura de crianças e adolescentes com doença renal crônica em tratamento conservador
(Universidade Federal de Minas GeraisUFMG, 2012-03-01)
The purpose of this study was to evaluate the evolution of anthropometric parameters of children and adolescents with chronic kidney disease (CKD) in conservative treatment. Measurements of weight, stature and biochemical ...
Fatores preditivos de progressão da doença renal crônica em umacoorte de crianças e adolescentes em tratamento conservador: desenvolvimento de um modelo clínico preditivo de risco
(Universidade Federal de Minas GeraisUFMG, 2012-06-13)
Objective: This retrospective cohort study was observational longitudinal carried out in order to develop a model to predict risk for CKD terminal using demographic, clinical and laboratory features of children and adolescents ...
Avaliação do estado nutricional de pacientes portadores de Doença Renal Policística Autossômica Dominante e sua associação com parâmetros clínicos e laboratoriais preditores de progressão
(Universidade Federal de São Paulo, 2021)
Introdução: A Doença Renal Policística Autossômica Dominante (DRPAD) é uma nefropatia de origem hereditária, mas apesar do caráter genético, vários fatores potencialmente modificáveis como os de caráter clínico, laboratorial, ...