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18篇 您的检索式:作者名="RINAT C"
    题名 作者 年代 出处 被引量
1Mutations in NPHS2 encoding podocin are a prevalent cause of steroid- resistant nephrotic syndrome among Israeli-Arab children 显示文摘Frishberg Y Rinat C Megged O 2002J Am Soc Nephrol2002,13,2:1
2Mutated podocin manifesting as CMV - associated congenital nephrotic syndrome 显示文摘Frishberg Y Rinat C Feinstein S 2003Pediatr Nephrol2003,18,3:1
3B-type natriuretic pep- tides are reliable markers of cardiac strain in CKD pediatric pa- tients显示文摘Rinat C Becker-Cohen R Nir A 2012Pediatr Nephrol2012,27,4:1
4Mutations in the mitochondrial seryl- tRNAsynthetase cause hyperuricemia, pulmonary hypertension, renal failure in infancy and alkalosis, HUPRA syndrome显示文摘Belostotsky R Ben-Shalom E Rinat C 2011Am J Hum Genet2011,88,2:1
5Familial inheritance of crossed fused renal ectopia显示文摘Rinat C Farkas A Frishberg Y 2001Pediatr Nephrol2001,16,3:1
6Mutations in NPHS2 encoding podocin are a prevalent cause of steroid-resistant nephrotic syndrome among Israeli-Arab children显示文摘Frishberg Y Rinat C Megged O 2002J Am Soc Nephrol2002,13,2:1
7Mutations in NPHS2 en- coding podoein are a prevalent cause of steroid-resistant nephrotic syndrome among Israeli-Arab children 显示文摘Frishberg Y Rinat C Megged O 2002J Am Soc Nephrol2002,13,6:1
8Mutated podocin manifesting as CMV-associated congenital nephrotic syndrome 显示文摘Frishberg Y Rinat C Feinstein S 2003Pediatr Nephrol2003,18,:1
9Mutations in NPHS2 encoding podocin are a prevalent cause of steroid-resistant nephrotic syndrome among Israeli-Arab children显示文摘FRISHBERG Y RINAT C MEGGED O 2002J Am Soc Nephrol2002,13,2:1
10Familial inheritance of crossed fused renal ectopia显示文摘Rinat C Farkas A Frishherg Y 2001Pediatr Nephrol2001,16,3:1
11Mutations in NPHS2encoding podocin are a prevalent cause of steroid-resistant nephrotic syndrome among Israeli-Arab children显示文摘Frishberg Y Rinat C Megged 0 2002J Am Soc Nephrol2002,13,2:1
12Genetic analysis-a diagnostic tool for primary hyperoxaluria type I 显示文摘Milosevic D Rinat C Batinic D 2002Pediatr Nephrol2002,17,11:1
13Is noncompliance among adolescent renal transplantrecipients inevitable?显示文摘Feinstein S Keich R Becker-Cohen R Rinat C Schwartz SB Frishberg Y 2005Pediatrics2005,115,4:1
14B-type natriuretic peptides are reliable markers of cardiac strain in CKD pediatric patients显示文摘Rinat C Cohen RB Sofia Feinstein AN 0,,:1
15Mutations in themitochondrial Seryl-tRNA synthetase cause hyperuricemia,pulmonary hypertension, renal failure in infancy and alkalosis, HUPRAsyndrome 显示文摘Belostotsky R Ben-Shalom E Rinat C 2011Am J Hum Genet2011,88,2:1
16Familial inheritance of crossed fused renal ectopia 显示文摘Rinat C Farkas A Frishberg Y 2001Pediatr Nephrol2001,16,3:1
17Reaction pathways显示文摘Sutherland I W Hamilton N G Dudman C C Chlo- rination and dehydrochlorination reactions relevant to the manufacture of trichloroethene and tetrachloroethene Part 1 2011Applied Catalysis A: General2011,1,399:1
18Risk factors for cardiovascular disease in children and young adults after renal transplantation显示文摘Becker-Cohen R Nir A Rinat C 2006Clin J Am Soc Nephrol2006,1,6:1
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