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Year Number of Results
1951 1
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1982 2
1984 4
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1986 5
1987 7
1988 10
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1990 13
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1992 16
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1994 25
1995 30
1996 16
1997 25
1998 36
1999 32
2000 30
2001 30
2002 38
2003 41
2004 53
2005 49
2006 47
2007 29
2008 52
2009 39
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1,399 results

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Page 1
The genetics of Autosomal Recessive Polycystic Kidney Disease (ARPKD).
Goggolidou P, Richards T. Goggolidou P, et al. Biochim Biophys Acta Mol Basis Dis. 2022 Apr 1;1868(4):166348. doi: 10.1016/j.bbadis.2022.166348. Epub 2022 Jan 12. Biochim Biophys Acta Mol Basis Dis. 2022. PMID: 35032595 Free article. Review.
ARPKD is a genetically inherited kidney disease that manifests by bilateral enlargement of cystic kidneys and liver fibrosis. ...
ARPKD is a genetically inherited kidney disease that manifests by bilateral enlargement of cystic kidneys and liver fibrosis. …
Autosomal Recessive Polycystic Kidney Disease: Diagnosis, Prognosis, and Management.
Burgmaier K, Broekaert IJ, Liebau MC. Burgmaier K, et al. Adv Kidney Dis Health. 2023 Sep;30(5):468-476. doi: 10.1053/j.akdh.2023.01.005. Adv Kidney Dis Health. 2023. PMID: 38097335 Review.
Autosomal recessive polycystic kidney disease (ARPKD) is the rare and usually early-onset form of polycystic kidney disease with a typical clinical presentation of enlarged cystic kidneys and liver involvement with congenita …
Autosomal recessive polycystic kidney disease (ARPKD) is the rare and usually early-onset form of poly …
Consensus expert recommendations for the diagnosis and management of autosomal recessive polycystic kidney disease: report of an international conference.
Guay-Woodford LM, Bissler JJ, Braun MC, Bockenhauer D, Cadnapaphornchai MA, Dell KM, Kerecuk L, Liebau MC, Alonso-Peclet MH, Shneider B, Emre S, Heller T, Kamath BM, Murray KF, Moise K, Eichenwald EE, Evans J, Keller RL, Wilkins-Haug L, Bergmann C, Gunay-Aygun M, Hooper SR, Hardy KK, Hartung EA, Streisand R, Perrone R, Moxey-Mims M. Guay-Woodford LM, et al. J Pediatr. 2014 Sep;165(3):611-7. doi: 10.1016/j.jpeds.2014.06.015. Epub 2014 Jul 9. J Pediatr. 2014. PMID: 25015577 Free PMC article.
Autosomal recessive polycystic kidney disease (ARPKD; MIM 263200) is a severe, typically early onset form of cystic disease that primarily involves the kidneys and biliary tract. ...The meeting was funded by the National Institutes of Hea …
Autosomal recessive polycystic kidney disease (ARPKD; MIM 263200) is a severe, typically early onset form …
Cilia and polycystic kidney disease.
Ma M. Ma M. Semin Cell Dev Biol. 2021 Feb;110:139-148. doi: 10.1016/j.semcdb.2020.05.003. Epub 2020 May 28. Semin Cell Dev Biol. 2021. PMID: 32475690 Review.
Polycystic kidney disease (PKD), comprising autosomal dominant polycystic kidney disease (ADPKD) and autosomal recessive polycystic kidney disease (ARPKD), is characterized by incessant cyst forma …
Polycystic kidney disease (PKD), comprising autosomal dominant polycystic kidney disease (A …
Molecular Pathophysiology of Autosomal Recessive Polycystic Kidney Disease.
Cordido A, Vizoso-Gonzalez M, Garcia-Gonzalez MA. Cordido A, et al. Int J Mol Sci. 2021 Jun 17;22(12):6523. doi: 10.3390/ijms22126523. Int J Mol Sci. 2021. PMID: 34204582 Free PMC article. Review.
Autosomal recessive polycystic kidney disease (ARPKD) is a rare disorder and one of the most severe forms of polycystic kidney disease, leading to end-stage renal disease (ESRD) in childhood. ...However, the function …
Autosomal recessive polycystic kidney disease (ARPKD) is a rare disorder and one of the most severe forms …
Refining genotype-phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants.
Burgmaier K, Brinker L, Erger F, Beck BB, Benz MR, Bergmann C, Boyer O, Collard L, Dafinger C, Fila M, Kowalewska C, Lange-Sperandio B, Massella L, Mastrangelo A, Mekahli D, Miklaszewska M, Ortiz-Bruechle N, Patzer L, Prikhodina L, Ranchin B, Ranguelov N, Schild R, Seeman T, Sever L, Sikora P, Szczepanska M, Teixeira A, Thumfart J, Uetz B, Weber LT, Wühl E, Zerres K; ESCAPE Study group; GPN study group; Dötsch J, Schaefer F, Liebau MC; ARegPKD consortium. Burgmaier K, et al. Kidney Int. 2021 Sep;100(3):650-659. doi: 10.1016/j.kint.2021.04.019. Epub 2021 Apr 30. Kidney Int. 2021. PMID: 33940108
Autosomal recessive polycystic kidney disease (ARPKD) is a severe disease of early childhood that is clinically characterized by fibrocystic changes of the kidneys and the liver. ...Patients with two missense variants affecting amino acid …
Autosomal recessive polycystic kidney disease (ARPKD) is a severe disease of early childhood that …
Early clinical management of autosomal recessive polycystic kidney disease.
Liebau MC. Liebau MC. Pediatr Nephrol. 2021 Nov;36(11):3561-3570. doi: 10.1007/s00467-021-04970-8. Epub 2021 Feb 17. Pediatr Nephrol. 2021. PMID: 33594464 Free PMC article. Review.
Autosomal recessive polycystic kidney disease (ARPKD) is a rare but highly relevant disorder in pediatric nephrology. ...ARPKD frequently presents perinatally, and the management of perinatal and early disease symptoms may be challenging. …
Autosomal recessive polycystic kidney disease (ARPKD) is a rare but highly relevant disorder in pediatric …
Predictors of progression in autosomal dominant and autosomal recessive polycystic kidney disease.
Benz EG, Hartung EA. Benz EG, et al. Pediatr Nephrol. 2021 Sep;36(9):2639-2658. doi: 10.1007/s00467-020-04869-w. Epub 2021 Jan 21. Pediatr Nephrol. 2021. PMID: 33474686 Free PMC article. Review.
Autosomal dominant polycystic kidney disease (ADPKD) and autosomal recessive polycystic kidney disease (ARPKD) are characterized by bilateral cystic kidney disease leading to progressive kidney fu …
Autosomal dominant polycystic kidney disease (ADPKD) and autosomal recessive polycystic …
Autosomal recessive polycystic kidney disease.
Society for Maternal-Fetal Medicine (SMFM); Swanson K. Society for Maternal-Fetal Medicine (SMFM), et al. Am J Obstet Gynecol. 2021 Nov;225(5):B7-B8. doi: 10.1016/j.ajog.2021.06.038. Epub 2021 Sep 8. Am J Obstet Gynecol. 2021. PMID: 34507795 No abstract available.
Transplantation in autosomal recessive polycystic kidney disease: liver and/or kidney?
Chandar J, Garcia J, Jorge L, Tekin A. Chandar J, et al. Pediatr Nephrol. 2015 Aug;30(8):1233-42. doi: 10.1007/s00467-014-2887-3. Epub 2014 Aug 13. Pediatr Nephrol. 2015. PMID: 25115876 Review.
Autosomal recessive polycystic kidney disease (ARPKD) is characterized by enlarged kidneys with dilated collecting ducts and congenital hepatic fibrosis. ...In the presence of significant liver disease and ESKD, consideration should be gi …
Autosomal recessive polycystic kidney disease (ARPKD) is characterized by enlarged kidneys with dilated c …
1,399 results