Autosomal dominant tubulointerstitial kidney disease (ADTKD) in Ireland-Reference-Cited by-同舟云学术

Autosomal dominant tubulointerstitial kidney disease (ADTKD) in Ireland

Published:2019-01-01 Issue:1 Volume:41 Page:832-841
ISSN:0886-022X
Container-title:Renal Failure
language:en
Short-container-title:Renal Failure

Author:

Cormican S.¹,Connaughton D. M.¹²³,Kennedy C.¹⁴,Murray S.¹⁴,Živná M.⁵,Kmoch S.⁵,Fennelly N. K.⁶,O’Kelly P.¹,Benson K. A.¹⁴,Conlon E. T.¹,Cavalleri G.⁴,Foley C.³⁷,Doyle B.⁶,Dorman A.⁶,Little M. A.³⁸,Lavin P.⁸,Kidd K.⁹,Bleyer A. J.⁹,Conlon P. J.¹⁴

Affiliation:

1. Nephrology Department, Beaumont Hospital, Dublin, Ireland;

2. Department of Medicine, Boston Children’s Hospital, Harvard Medical School, Boston, MA, USA;

3. Trinity Health Kidney Centre, Trinity Translational Medicine Institute, Dublin, Ireland;

4. Department of Medicine, Royal College of Surgeons, Dublin, Ireland;

5. Department of Pediatrics and Adolescent Medicine, Research Unit for Rare Diseases, First Faculty of Medicine, Charles University, Prague, Czech Republic;

6. Pathology Department, Beaumont Hospital, Dublin, Ireland;

7. Clinical Research Centre, Royal College of Surgeons, Dublin, Ireland;

8. Trinity Health Kidney Centre, Tallaght Hospital, Dublin, Ireland;

9. Section on Nephrology, Wake Forest School of Medicine, Winston-Salem, NC, USA

Publisher

Informa UK Limited

Subject

Nephrology,Critical Care and Intensive Care Medicine,General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/0886022X.2019.1655452

Reference34 articles.

1. Autosomal dominant tubulointerstitial kidney disease: of names and genes

2. Diagnosis, management, and prognosis of HNF1B nephropathy in adulthood

3. Medicine M-N. Online Mendelian inheritance in man. An online catalog of human genes and genetic disorders [Website]. John Hopkins University: OMIM; 2018 [updated 2018 Sep 7]. Available from: https://www.omim.org.

4. Heterozygous Loss-of-Function SEC61A1 Mutations Cause Autosomal-Dominant Tubulo-Interstitial and Glomerulocystic Kidney Disease with Anemia

5. Variable Clinical Presentation of an MUC1 Mutation Causing Medullary Cystic Kidney Disease Type 1

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