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Outcome of renal transplantation in patients with autosomal dominant polycystic kidney disease
(SOC MEDICA SANTIAGO, 2012)
Background: Patients with autosomal dominant polycystic kidney disease (ADPKD) have a better survival in chronic dialysis than patients with other etiologies of renal failure. It has been suggested that extra-renal ...
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 ...
Molecular and cellular pathogenesis of autosomal dominant polycystic kidney disease
(Associação Brasileira de Divulgação Científica, 2011)
Autosomal dominant polycystic kidney disease (ADPKD) is one of the most common human life-threatening monogenic disorders. The disease is characterized by bilateral, progressive renal cystogenesis and cyst and kidney ...
Frequency and clinical profile of patients with polycystic kidney disease in Southern Brazil
(TAYLOR & FRANCIS INC, 2008)
Background. Autosomal dominant polycystic kidney disease (ADPKD) is one of the most common genetic nephropathies, affecting one in every 800-1000 individuals in the worldwide general population and 5-10% of hemodialysis ...
Congenital hepatic fibrosis. Report of five cases.
(2004)
Background. Congenital hepatic fibrosis (CHF) is an autosomic dominant disease that has been associated with polycystic kidney disease. Aim: To describe the medical management of 5 children with CHF and to evaluate the ...
Caffeine intake by patients with autosomal dominant polycystic kidney disease
(Associação Brasileira de Divulgação Científica, 2012-09-01)
Because caffeine may induce cyst and kidney enlargement in autosomal dominant polycystic kidney disease (ADPKD), we evaluated caffeine intake and renal volume using renal ultrasound in ADPKD patients. Caffeine intake was ...
Señalización celular de enfermedades crónicas no transmisibles: Revisión de la poliquistosis renal
(Ediciones Universidad Simón BolívarFacultad de Ciencias de la Salud, 2021-06)
Antecedentes: La poliquistosis renal es una enfermedad genética que afecta a más de 13 millones de personas a nivel mundial, siguiendo el patrón de herencia mendeliano al transmitirse de forma autosómica dominante o ...
Influence of ACE I/D gene polymorphism in the progression of renal failure in autosomal dominant polycystic kidney disease: a meta-analysis
(Oxford Univ Press, 2006-11-01)
Background. Autosomal dominant polycystic kidney disease (ADPKD) is a renal disease characterized by an important variability in clinical course, which cannot be fully explained by the genetic heterogeneity of the disease. ...
Avaliação do consumo de cafeína em pacientes com Doença Renal Policística Autossômica Dominante (DRPAD)
(Universidade Federal de São Paulo (UNIFESP), 2010-10-27)
A cafeína tem sido considerada um fator de risco para o crescimento dos cistos na Doença Renal Policística Autossômica Dominante (DRPAD) devido ao aumento de secreção de fluido e proliferação celular induzidos pelo acúmulo ...