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1. Early clinical management of autosomal recessive polycystic kidney disease.
2. Clinical features of autosomal recessive polycystic kidney disease in the Japanese population and analysis of splicing in PKHD1 gene for determination of phenotypes.
3. Systematic review on outcomes used in clinical research on autosomal recessive polycystic kidney disease-are patient-centered outcomes our blind spot?
4. [Gene variant analysis of a fetus with autosomal recessive polycystic kidney disease].
5. [Clinical characteristics and genetic analysis of a child with autosomal recessive polycystic kidney disease].
6. Contributions of afferent and sympathetic renal nerves to cystogenesis and arterial pressure regulation in a preclinical model of autosomal recessive polycystic kidney disease.
7. Clinical characteristics of Slovenian pediatric patients with autosomal recessive polycystic kidney disease.
8. Refining genotype-phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants.
9. Genetic autopsy and genetic counseling for a case of fatal oligohydramnios due to de novo 17q12 deletion syndrome.
10. The molecular structure and function of fibrocystin, the key gene product implicated in autosomal recessive polycystic kidney disease (ARPKD).