Clinical aspects of autosomal recessive polycystic kidney disease
Dias, Natasha Favoretto; Lanzarini, Vivian; Onuchic, Luiz Fernando; Koch, Vera Hermina Kalika.
J. bras. nefrol
; 32(3): 263-267, jul.-set. 2010. tab
Artigo em Português | LILACS | ID: lil-562918
Documentos relacionados
Clinical characteristics of Slovenian pediatric patients with autosomal recessive polycystic kidney disease.
Early clinical management of autosomal recessive polycystic kidney disease.
Contributions of afferent and sympathetic renal nerves to cystogenesis and arterial pressure regulation in a preclinical model of autosomal recessive polycystic kidney disease.
Autosomal recessive polycystic kidney disease.
The molecular structure and function of fibrocystin, the key gene product implicated in autosomal recessive polycystic kidney disease (ARPKD).
Systematic review on outcomes used in clinical research on autosomal recessive polycystic kidney disease-are patient-centered outcomes our blind spot?
Refining genotype-phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants.
Clinical features of autosomal recessive polycystic kidney disease in the Japanese population and analysis of splicing in PKHD1 gene for determination of phenotypes.
[Gene variant analysis of a fetus with autosomal recessive polycystic kidney disease].
[Clinical characteristics and genetic analysis of a child with autosomal recessive polycystic kidney disease].