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| 1 | Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible显示文摘 | Hinkes B Wiggins R C Gbadegesin R Vlangos C N Seelow D Nurnberg G | 2006 | Nat Genet2006，38，： | 1 |
| 2 | Mutational analysis of NPHS2 and WT1 in frequently relapsing and steroid -dependent nephrotie syndrome显示文摘 | Gbadegesin R Hinkes B Vlangos C | 2007 | Pediatr Nephrol2007，22，4： | 1 |
| 3 | Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS) 显示文摘 | Gbadegesin R Hinkes B G Hoskins B E Vlangos C N Heerin ga S F Liu J | 2008 | Nephrol Dial Transplant2008，23，： | 1 |
| 4 | Nephrotic syndrome in the first year of life: Two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2) 显示文摘 | Hinkes BG Mucha B Vlangos CN | 2007 | Pediatrics2007，119，4： | 1 |
| 5 | Nephrotic syndrome in the first year of life : Two thirds of cases are caused by mutations in 4 genes ( NPHS1, NPHS2, WT1, and LAMB2 ) 显示文摘 | Hinkes BG Mucha B Vlangos CN | 2007 | Pediatrics2007，119，4： | 1 |
| 6 | Mutationalanalysis of NPHS2 and WT1 in frequently relapsing andsteroid-dependent nephrotic syndrome 显示文摘 | Gbadegesin R Hinkes B Vlangos C | 2007 | Pediatr Nephrol2007，22，4： | 1 |
| 7 | Nephrotic syndrome in the first year of life:two thirds of cases are caused by mutations in 4 genes (NPHS1,NPHS2,WT1,and LAMB2)显示文摘 | Hinkes BG Mucha B Vlangos CN | | 0，，04： | 1 |
| 8 | Nephroticsyndrome in the first year of life: two thirds of cases arecaused by mutations in 4 genes (NPHS1, NPHS2, WT1, andLAMB2)显示文摘 | Hinkes B G Mucha B Vlangos C N | 2007 | Pediatrics2007，119，4： | 1 |
| 9 | Mutations in RAIl associated with Smith-Magenis syndrome 显示文摘 | Slager RE Newton TL Vlangos CN | 2003 | Nat Genet2003，33，4： | 1 |
| 10 | Nephrotic syndrome in the first year of life:two thirds of cases are caused by mutations in 4 genes (NPHS1,NPHS2,WT1,and LAMB2)显示文摘 | Hinkes B Mucha B Vlangos C | 2007 | Pediatrics2007，119，4： | 1 |
| 11 | Specific podocin mutations correlate with age of onset in steroid-resistant nephrotic syndrome显示文摘 | Hinkes B Vlangos C Heeringa S | 2008 | J Am Soc Nephrol2008，19，2： | 1 |
| 12 | Nephrotic syndrome in the first year of life : Two thirds of cases are caused by mutations in 4 genes ( NPHS1, NPHS2, WT1, and LAMB2 ) 显示文摘 | Hinkes BG Mucha B Vlangos CN | 2007 | Pediatrics2007，119，4： | 1 |
| 13 | Specific podoein mutations correlate with age of onset in steroid - resistant nephrotic syndrome 显示文摘 | Hinkes B Vlangos C Heeringa S | 2008 | J Am Soc Nephrol2008，19，2： | 1 |
| 14 | Nephrotic syndrome in the first year of life : two thirds of cases are caused by muta- tions in 4 genes (NPHS1 ,NPHS2,WT1 ,and LAMB2) 显示文摘 | Hinkes BG Mucha B Vlangos CN | 2007 | Pe- diatrics2007，119，4： | 1 |
| 15 | Specific podocin mutations correlate with age of onset in steroid-resistant nephrotic syndrome 显示文摘 | Hinkes B Vlangos C Heeringa S | 2008 | J Am Soc Nephrol2008，19，2： | 1 |
| 16 | Specific podocin mutations correlate with age of onset in steroid-resistant nephrotic syndrome显示文摘 | Hinkes B Vlangos C Heeringa S | 2008 | J Am Soc Nephrol2008，19，2： | 1 |
| 17 | Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome显示文摘 | HEERINGA S F VLANGOS C N CHERNIN G | 2008 | Nephrol Dial Transplant2008，23，11： | 1 |
| 18 | Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotie syndrome 显示文摘 | Heeringa SF Vlangos CN Chemin G | 2008 | Nephrol Dial Transplant2008，23，11： | 1 |
| 19 | Nephrotic syndrome in the first year of life : Two thirds of cases are caused by mutations in 4 genes ( NPHS1, NPHS2, WT1, and LAMB2 ) 显示文摘 | Hinkes BG Mucha B Vlangos CN | 2007 | Pediatrics2007，119，4： | 1 |
| 20 | Nephroticsyndrome in the first year of life: two thirds of cases arecaused by mutations in 4 genes (NPHSl, NPHS2, WTl, andLAMB2) 显示文摘 | Hinkes BG Mucha B Vlangos CN et a1 | 2007 | Pediatrics2007，119，4： | 1 |
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