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Page 1
Renal complications in 6p duplication syndrome: microarray-based investigation of the candidate gene(s) for the development of congenital anomalies of the kidney and urinary tract (CAKUT) and focal segmental glomerular sclerosis (FSGS).
Am J Med Genet A. 2015 Mar;167A(3):592-601. doi: 10.1002/ajmg.a.36942.
Am J Med Genet A. 2015.
PMID: 25691411
Review.
Morbidity in children with frequently relapsing nephrosis: 10-year follow-up of a randomized controlled trial.
Ishikura K, Yoshikawa N, Nakazato H, Sasaki S, Nakanishi K, Matsuyama T, Ito S, Hamasaki Y, Yata N, Ando T, Iijima K, Honda M; Japanese Study Group of Renal Disease in Children.
Ishikura K, et al.
Pediatr Nephrol. 2015 Mar;30(3):459-68. doi: 10.1007/s00467-014-2955-8. Epub 2014 Oct 3.
Pediatr Nephrol. 2015.
PMID: 25277597
Clinical Trial.
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