van't Hoff WG - Search Results

1

Incompletely penetrant PKD1 alleles suggest a role for gene dosage in cyst initiation in polycystic kidney disease.

Rossetti S, Kubly VJ, Consugar MB, Hopp K, Roy S, Horsley SW, Chauveau D, Rees L, Barratt TM, van't Hoff WG, Niaudet P, Torres VE, Harris PC. Rossetti S, et al. Kidney Int. 2009 Apr;75(8):848-55. doi: 10.1038/ki.2008.686. Epub 2009 Jan 21. Kidney Int. 2009. PMID: 19165178 Free PMC article.

2

An association of tubular dysfunction, cortical macrocysts and chronic kidney disease.

Bockenhauer D, Rees L, van't Hoff W. Bockenhauer D, et al. Pediatr Nephrol. 2006 Apr;21(4):580-3. doi: 10.1007/s00467-006-0009-6. Epub 2006 Mar 1. Pediatr Nephrol. 2006. PMID: 16508772

3

Are there guidelines for a strategy according to glomerular filtration rate, plasma oxalate determination and the risk of oxalate accumulation?

Barratt TM, van't Hoff WG. Barratt TM, et al. Nephrol Dial Transplant. 1995;10 Suppl 8:22-3. doi: 10.1093/ndt/10.supp8.22. Nephrol Dial Transplant. 1995. PMID: 8592620 No abstract available.

4

Atypical familial juvenile hyperuricemic nephropathy associated with a hepatocyte nuclear factor-1beta gene mutation.

Bingham C, Ellard S, van't Hoff WG, Simmonds HA, Marinaki AM, Badman MK, Winocour PH, Stride A, Lockwood CR, Nicholls AJ, Owen KR, Spyer G, Pearson ER, Hattersley AT. Bingham C, et al. Kidney Int. 2003 May;63(5):1645-51. doi: 10.1046/j.1523-1755.2003.00903.x. Kidney Int. 2003. PMID: 12675839 Free article.

5

The use of steroid-sparing agents in steroid-sensitive nephrotic syndrome.

Abeyagunawardena AS, Dillon MJ, Rees L, van't Hoff W, Trompeter RS. Abeyagunawardena AS, et al. Pediatr Nephrol. 2003 Sep;18(9):919-24. doi: 10.1007/s00467-003-1216-z. Epub 2003 Jul 23. Pediatr Nephrol. 2003. PMID: 12883981

6

A fatal case of cerebral oedema with hyponatraemia and massive polyuria after renal transplantation.

Cansick J, Rees L, Koffman G, Van't Hoff W, Bockenhauer D. Cansick J, et al. Pediatr Nephrol. 2009 Jun;24(6):1231-4. doi: 10.1007/s00467-008-1100-y. Epub 2009 Jan 20. Pediatr Nephrol. 2009. PMID: 19153773

7

Clinico-pathological correlations of congenital and infantile nephrotic syndrome over twenty years.

Kari JA, Montini G, Bockenhauer D, Brennan E, Rees L, Trompeter RS, Tullus K, Van't Hoff W, Waters A, Ashton E, Lench N, Sebire NJ, Marks SD. Kari JA, et al. Pediatr Nephrol. 2014 Nov;29(11):2173-80. doi: 10.1007/s00467-014-2856-x. Epub 2014 Jun 6. Pediatr Nephrol. 2014. PMID: 24902943 Free PMC article.

8

Presymptomatic detection of familial juvenile hyperuricaemic nephropathy in children.

McBride MB, Rigden S, Haycock GB, Dalton N, Van't Hoff W, Rees L, Raman GV, Moro F, Ogg CS, Cameron JS, Simmonds HA. McBride MB, et al. Pediatr Nephrol. 1998 Jun;12(5):357-64. doi: 10.1007/s004670050466. Pediatr Nephrol. 1998. PMID: 9686952

9

Childhood thin GBM disease: review of 22 children with family studies and long-term follow-up.

Carasi C, Van't Hoff WG, Rees L, Risdon RA, Trompeter RS, Dillon MJ. Carasi C, et al. Pediatr Nephrol. 2005 Aug;20(8):1098-105. doi: 10.1007/s00467-005-1879-8. Epub 2005 Jun 7. Pediatr Nephrol. 2005. PMID: 15940548

10

Catch-up growth with normal parathyroid hormone levels in chronic renal failure.

Waller S, Ledermann S, Trompeter R, van't Hoff W, Ridout D, Rees L. Waller S, et al. Pediatr Nephrol. 2003 Dec;18(12):1236-41. doi: 10.1007/s00467-003-1284-0. Epub 2003 Oct 30. Pediatr Nephrol. 2003. PMID: 14586680

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