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Detection of large deletion mutations in the COL4A5 gene of female Alport syndrome patients.
Pediatr Nephrol. 2008 Nov;23(11):2085-90. doi: 10.1007/s00467-008-0878-y. Epub 2008 Jun 27.
Pediatr Nephrol. 2008.
PMID: 18584212
The effect of aldosterone blockade in patients with Alport syndrome.
Kaito H, Nozu K, Iijima K, Nakanishi K, Yoshiya K, Kanda K, Przybyslaw Krol R, Yoshikawa N, Matsuo M.
Kaito H, et al. Among authors: przybyslaw krol r.
Pediatr Nephrol. 2006 Dec;21(12):1824-9. doi: 10.1007/s00467-006-0270-8. Epub 2006 Oct 13.
Pediatr Nephrol. 2006.
PMID: 17039334
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A novel mutation in KCNJ1 in a Bartter syndrome case diagnosed as pseudohypoaldosteronism.
Nozu K, Fu XJ, Kaito H, Kanda K, Yokoyama N, Przybyslaw Krol R, Nakajima T, Kajiyama M, Iijima K, Matsuo M.
Nozu K, et al. Among authors: przybyslaw krol r.
Pediatr Nephrol. 2007 Aug;22(8):1219-23. doi: 10.1007/s00467-007-0468-4. Epub 2007 Mar 31.
Pediatr Nephrol. 2007.
PMID: 17401586
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