The clinical complexity of PKHD1 gene: from neonatal lethality to casual diagnosis in late pediatric stages-Reference-Cited by-同舟云学术

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The clinical complexity of PKHD1 gene: from neonatal lethality to casual diagnosis in late pediatric stages

Published:2024-06 Issue:6 Volume:100 Page:467-471
ISSN:2341-2879
Container-title:Anales de Pediatría (English Edition)
language:en
Short-container-title:Anales de Pediatría (English Edition)

Author:

Rubio-Granda Ana,Gil-Peña Helena,Rodríguez-Márquez Carlos,Solís-Sánchez Gonzalo,Ordóñez-Álvarez Flor Angel

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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