• Nenhum resultado encontrado

Renal and extrarenal manifestations of autosomal dominant polycystic kidney disease

N/A
N/A
Protected

Academic year: 2019

Share "Renal and extrarenal manifestations of autosomal dominant polycystic kidney disease"

Copied!
6
0
0

Texto

Loading

Imagem

Table 1. Clinical and laboratory data of patients with autosomal dominant polycystic kidney disease.
Table 2. Intracranial alterations in patients with autosomal dominant polycystic kidney disease.

Referências

Documentos relacionados

Indications for unilateral nephrectomy were pyonephrosis in 6 patients (one of them with adult polycystic kidney disease - APKD) and giant hydro- nephrosis without a

Materials and Methods: We retrospectively reviewed the charts of 18 patients with symptomatic autosomal dominant polycystic kidney disease who underwent bilateral hand

BACKGROUND: Patients with end-stage renal failure due to huge autosomal dominant polycystic kidney disease usually have an umbilical hernia and rectus abdominis diastasis, which

Cyst infection in hospital-admitted autosomal dominant polycystic kidney disease patients is predominantly multifocal and associated with kidney and liver

In a general framework, Ang and Bekaert (2002a, 2004) show that regime- switching dynamics should be incorporated in asset allocation strategies. Although it is common to treat

(2017) – Controlo estrutural de mineralizações de Cobre na Mina dos Mociços (Zona de Ossa-Morena); dados preliminares.. (1991) – Traços gerais da

Patients with adult polycystic disease and symptoms of pain or discomfort can ben- efit from these minimally invasive procedures through decortication surgery, performed on kidney

Quality of life was evaluated by the Kidney Disease and Quality of Life Short- Form, pain by the Brief Pain Inventory, emotional factors by Beck anxiety and depression scales