Polycystic Kidney Disease
Mostrando 1-12 de 156 artigos, teses e dissertações.
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1. NOS3 gene intron 4 a/b polymorphism is associated with ESRD in autosomal dominant polycystic kidney disease patients
Resumo Introdução: Genes da óxido nítrico sintase endotelial (eNOS) têm sido implicados na hemodinâmica renal como potentes reguladores do tônus vascular e pressão arterial. Tem sido vinculado a uma redução nos níveis plasmáticos de óxido nítrico. Realizou-se recentemente vários estudos para investigar o papel de polimorfismos do gene NOS3 e
Brazilian Journal of Nephrology. Publicado em: 2022
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2. Refractory ascites and graft dysfunction in early renal transplantation
Resumo A ocorrência de ascite no pós-Transplante Renal (TR) é infrequente, podendo ser consequência de complicações cirúrgicas ou médicas. Caso clínico: 61 anos, masculino, antecedentes de hipertensão arterial, carcinoma da língua e hábitos alcoólicos 12-20g/dia. Doença renal crônica secundária à doença renal poliquística autossômica domi
J. Bras. Nefrol.. Publicado em: 18/03/2019
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3. Retroperitoneoscopic nephrectomy for huge autosomal-dominant polycystic kidney disease using morcellator
ABSTRACT Introduction and Objectives: Nephrectomy is occasionally required due to severe extra-renal symptom(s) such as dyspepsia in patients with autosomal dominant polycystic kidney disease (ADPKD), wherein a large incision is required for specimen extraction. Considering problems such as hernia, wound dehiscence, incidental bowel injury, and poor wound h
Int. braz j urol.. Publicado em: 2018-06
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4. Robotic Assisted Radical Cystoprostatectomy and Intracorporeal Ileal Conduit Urinary Diversion for a Kidney Transplant Recipient
ABSTRACT Introduction and Objectives: Robotic assisted radical cystectomy (RARC) is an alternative to open radical cystectomy. As experience is gained with the RARC approach the technique is being applied to more complex surgical cases. We describe here our technique for RARC with intracorporeal ileal conduit urinary diversion for a renal transplant recipie
Int. braz j urol.. Publicado em: 2017-12
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5. Sociodemographic characteristics and clinical features of patients with adult polycystic kidney disease undergoing hemodialysis; Características sociodemográficas e aspectos clínicos de pacientes com doença renal policística do adulto submetidos a hemodiá
AIMS: To analyze the sociodemographic and clinical characteristics of patients with adult polycystic kidney disease admitted to hemodialysis services in Northwestern Paraná state, Brazil. METHODS: This was an observational, descriptive and retrospective longitudinal study. Medical records of patients with polycystic kidneys who initiated hemodialysis betwee
Publicado em: 08/05/2015
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6. Autosomal dominant polycystic kidney disease in hemodialysis patients in southern Brazil; Doença renal policística autossômica dominante em pacientes em hemodiálise no sul
Introduction: Autosomal dominant polycystic kidney disease is the most common hereditary renal disease in humans. Objective: To examine the prevalence, clinical and laboratory characteristics of patients with polycystic kidneys and relate disease manifestations by gender. Methods: This was an observational and retrospective study. All the medical records of
Publicado em: 08/05/2015
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7. Autosomal dominant polycystic kidney disease: possible influences of single nucleotide polymorphism in cytokine genes; Doença renal policística autossômica dominante: possíveis influências de polimorfismos de um único nucleotídeo em genes de citocinas
Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited diseases in adults and is caused by mutations in one of two genes, PKD1 or PKD2, which result in accumulation of cysts in the kidneys that can lead to a loss of function. Is the third leading cause of chronic kidney disease (CKD) stage 5. Inflammation has been considered one of
Publicado em: 08/05/2015
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8. Estudo de associação entre os polimorfismos de um único nucleotídeo em genes de citocinas e a doença renal policística autossômica dominante em uma população brasileira
A doença Renal Policística Autossômica Dominante (DRPAD) é causada por mutações em um de dois genes, PKD1 ou PKD2, que resultam em acúmulos de cistos nos rins. O objetivo deste trabalho foi verificar a existência de possíveis associações entre variantes em genes de citocinas e em receptores de citocinas para as posições IL1A-889 (rs1800587), IL1
Publicado em: 03/02/2015
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9. Cyst infection in hospital-admitted autosomal dominant polycystic kidney disease patients is predominantly multifocal and associated with kidney and liver volume
Positron-emission tomography/computed tomography (PET/CT) has improved cyst infection (CI) management in autosomal dominant polycystic kidney disease (ADPKD). The determinants of kidney and/or liver involvement, however, remain uncertain. In this study, we evaluated clinical and imaging factors associated with CI in kidney (KCI) and liver (LCI) in ADPKD. A r
Braz J Med Biol Res. Publicado em: 13/06/2014
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10. O crescimento cístico renal é o principal determinante para o desenvolvimento de hipertensão e déficit de concentração em camundongos com deficiência do gene Pkd1 / Renal cyst growth is the main determinant for the development of hypertension and concentration deficit in Pkd1-deficient mice
O desenvolvimento de hipertensão arterial (HAS) ocorre dez anos mais cedo em pacientes com doença renal policística autossômica dominante (DRPAD) comparados à população geral, estando presente em ~60% dos indivíduos afetados antes da perda de função renal. Déficit de concentração renal também se constitui em um achado precoce nesses pacientes.
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 13/11/2012
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11. Caffeine intake by patients with autosomal dominant polycystic kidney disease
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 estimated by the average of 24-h dietary recalls obtained on 3 nonconsecutive days in 102 ADPKD patients (68 females, 34 males; 39 ± 12 ye
Brazilian Journal of Medical and Biological Research. Publicado em: 2012-09
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12. Mucinous cystadenoma of the appendix mimicking polycystic kidney disease
International braz j urol. Publicado em: 2012-04