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F1000Research, ISSN 2046-1402, 2019, Volume 8, p. 116
Autosomal dominant polycystic kidney disease (ADPKD) is a genetic systemic disorder causing the development of renal and hepatic cysts and decline in renal... 
ADPKD | Treatment | Diagnosis | Management | Prediction | Enzymes | Genetic disorders | Renal function | Kidneys | Polycystic kidney | Liver | Genes | Clinical trials | FDA approval | Patients | Proteins | Body mass index | Genetic counseling | Cysts | Fibrosis | Renal failure | Blood pressure | Mutation | Kidney diseases
Journal Article
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, ISSN 0931-0509, 06/2019, Volume 34, Issue 8, pp. 1272 - 1279
Alport syndrome (AS) is the most frequent inherited kidney disease after autosomal dominant polycystic kidney disease. It has three different patterns of... 
Journal Article
Medicina Clínica, ISSN 0025-7753, 2013, Volume 142, Issue 2, pp. 73 - 79
Resumen La poliquistosis renal autosómica dominante es la enfermedad renal hereditaria más frecuente. Carece de un tratamiento específico. Su prevalencia es de... 
Internal Medicine | Poliquistosis renal autosómica dominante | Patogénesis | Tratamiento | Treatment | Pathogenesis | Autosomal dominant polycystic kidney disease
Journal Article
Medicina Clinica, ISSN 0025-7753, 10/2017, Volume 149, Issue 7, p. 322
En este artículo publicado anteriormente, se han citado erróneamente algunos de los componentes indicados en el anexo. Los datos correctos son: 
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 09/2015, Volume 23, Issue 9, pp. 1192 - 1199
Journal Article
Kidney International, ISSN 0085-2538, 12/2008, Volume 74, Issue S111, pp. S29 - S32
Fabry disease is an X-linked lysosomal storage disorder that affects both sexes. Progressive cellular accumulation of glycolipids starts early in life and, if... 
renal outcome | treatment | agalsidase | renal pathology | Fabry | proteinuria | Agalsidase | Treatment | Proteinuria | Renal outcome | Renal pathology | INVOLVEMENT | FEMALES | ALPHA | ANTIBODY-FORMATION | NATURAL-HISTORY | OUTCOME SURVEY | NEPHROPATHY | UROLOGY & NEPHROLOGY | KIDNEY | ENZYME REPLACEMENT THERAPY | AGALSIDASE-BETA THERAPY
Journal Article
Clinical kidney journal, ISSN 2048-8505, 12/2018, Volume 11, Issue Suppl 1, p. i1
Journal Article
Clinical Kidney Journal, ISSN 2048-8505, 12/2018, Volume 11, Issue suppl_1, pp. i1 - i1
Journal Article
Clinical Kidney Journal, ISSN 2048-8505, 12/2018, Volume 11, Issue Suppl 1, pp. i1 - i1
Journal Article
Clinical Kidney Journal, ISSN 2048-8505, 12/2018, Volume 11, Issue suppl_1, pp. i1 - i1
Journal Article
Medicina Clinica, ISSN 0025-7753, 01/2014, Volume 142, Issue 2, pp. 73 - 79
Autosomal dominant polycystic kidney disease is the most frequent hereditary kidney disease. However it lacks a specific treatment. Its prevalence is 1/800 and... 
Pathogenesis | Autosomal dominant polycystic kidney disease | Treatment
Journal Article
Journal Article
Kidney International, ISSN 0085-2538, 03/2012, Volume 81, Issue 5, pp. 494 - 501
Journal Article
Journal Article
Kidney International, ISSN 0085-2538, 07/2015, Volume 88, Issue 1, pp. 17 - 27
Journal Article