End stage renal disease, differential diagnosis, a rare genetic disorder: bardet-biedl syndrome: case report and review.
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Update on the genetics of bardet-biedl syndromeAssociation of angiotensin II type-1 receptor A1166C gene polymorphism with the susceptibility of end-stage renal disease.Two brothers with bardet-biedl syndrome presenting with chronic renal failure.Bardet-biedl syndrome: a rare cause of chronic kidney disease.Association of endothelial nitric oxide synthase Glu298Asp gene polymorphism with the risk of end-stage renal disease.Association of endothelial nitric oxide synthase gene polymorphisms with end-stage renal disease: a systematic review and meta-analysis.Bardet-Biedl syndrome presenting with steroid sensitive nephrotic syndrome.
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P2860
End stage renal disease, differential diagnosis, a rare genetic disorder: bardet-biedl syndrome: case report and review.
description
2011 nî lūn-bûn
@nan
2011 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
End stage renal disease, diffe ...... drome: case report and review.
@ast
End stage renal disease, diffe ...... drome: case report and review.
@en
type
label
End stage renal disease, diffe ...... drome: case report and review.
@ast
End stage renal disease, diffe ...... drome: case report and review.
@en
prefLabel
End stage renal disease, diffe ...... drome: case report and review.
@ast
End stage renal disease, diffe ...... drome: case report and review.
@en
P2093
P2860
P1476
End stage renal disease, diffe ...... drome: case report and review.
@en
P2093
B Sowjanya
N Sivaranjani
U Sreenivasulu
P2860
P2888
P304
P356
10.1007/S12291-011-0116-4
P577
2011-02-04T00:00:00Z