Childhood Polycystic Kidney Disease
Author:
Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/978-3-662-43596-0_32
Reference409 articles.
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3. Hildebrandt F, Benzing T, Katsanis N. Ciliopathies. N Engl J Med. 2011;364(16):1533–43.
4. Valente EM, Dallapiccola B, Bertini E. Joubert syndrome and related disorders. Handb Clin Neurol. 2013;113:1879–88.
5. Barker AR, Thomas R, Dawe HR. Meckel-Gruber syndrome and the role of primary cilia in kidney, skeleton, and central nervous system development. Organogenesis. 2014;10(1):96–107.
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1. Complications and prognosis of patients diagnosed with autosomal recessive polycystic kidney disease in neonatal period;CEN Case Reports;2023-10-25
2. Nephronophthisis due to mutation in the TMEM67 gene;Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics);2022-06-10
3. Renal oligohydramnios and Potter sequence with cystic kidney disease;Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics);2021-03-31
4. Rapidly progressive nephromegaly in a neonate with autosomal recessive poly cystic kidney disease;Journal of Nephropathology;2017-07-19
5. Emerging Therapies for Childhood Polycystic Kidney Disease;Frontiers in Pediatrics;2017-04-19
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