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Mueller, Roman-Ulrich, Haas, Christian S. and Sayer, John A. 
ORCID: 0000-0003-1881-3782
(2018).
Practical approaches to the management of autosomal dominant polycystic kidney disease patients in the era of tolvaptan.
Clin. Kidney J., 11 (1).
S. 62 - 70.
OXFORD:
OXFORD UNIV PRESS.
ISSN 2048-8513
Braun, Daniela A., Schueler, Markus, Halbritter, Jan, Gee, Heon Yung ORCID: 0000-0002-8741-6177, Porath, Jonathan D., Lawson, Jennifer A., Airik, Rannar, Shril, Shirlee, Allen, Susan J., Stein, Deborah, Al Kindy, Adila, Beck, Bodo B., Cengiz, Nurcan, Moorani, Khemchand N., Ozaltin, Fatih, Hashmi, Seema, Sayer, John A. ORCID: 0000-0003-1881-3782, Bockenhauer, Detlef ORCID: 0000-0001-5878-941X, Soliman, Neveen A., Otto, Edgar A., Lifton, Richard P. and Hildebrandt, Friedhelm
(2016).
Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicity.
Kidney Int., 89 (2).
S. 468 - 476.
NEW YORK:
ELSEVIER SCIENCE INC.
ISSN 1523-1755
Beck, Bodo B., Trachtman, Howard ORCID: 0000-0001-7447-9489, Gitman, Michael, Miller, Ilene, Sayer, John A. ORCID: 0000-0003-1881-3782, Pannes, Andrea, Baasner, Anne, Hildebrandt, Friedhelm and Wolf, Matthias T. F.
(2011).
Autosomal Dominant Mutation in the Signal Peptide of Renin in a Kindred With Anemia, Hyperuricemia, and CKD.
Am. J. Kidney Dis., 58 (5).
S. 821 - 826.
PHILADELPHIA:
W B SAUNDERS CO-ELSEVIER INC.
ISSN 0272-6386