La complejidad clínica del gen PKHD1: de la letalidad perinatal al diagnóstico casual en etapas pediátricas tardías
Author:
Publisher
Elsevier BV
Reference6 articles.
1. Refining genotype–phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants;Burgmaier;Kidney Int.,2021
2. Diagnosis and Management of Renal Cystic Disease of the Newborn: Core Curriculum 2021;Raina;Am J Kidney Dis.,2021
3. Transplantation in autosomal recessive polycystic kidney disease: liver and/or kidney?;Chandar;Pediatr Nephrol.,2015
4. Early bilateral nephrectomy in neonatal autosomal recessive polycystic kidney disease: Improved prognosis or unnecessary effort?;Riechardt;Urologe A.,2017
5. Severe neurological outcomes after very early bilateral nephrectomies in patients with autosomal recessive polycystic kidney disease (ARPKD);Burgmaier;Sci Rep.,2020
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