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Autosomal recessive renal glucosuria attributable to a mutation in the sodium glucose cotransporter (SGLT2).
van den Heuvel LP, Assink K, Willemsen M, Monnens L. van den Heuvel LP, et al. Among authors: monnens l. Hum Genet. 2002 Dec;111(6):544-7. doi: 10.1007/s00439-002-0820-5. Epub 2002 Sep 27. Hum Genet. 2002. PMID: 12436245
Nephrogenic diabetes insipidus: close linkage with markers from the distal long arm of the human X chromosome.
Knoers N, van der Heyden H, van Oost BA, Ropers HH, Monnens L, Willems J. Knoers N, et al. Among authors: monnens l. Hum Genet. 1988 Sep;80(1):31-8. doi: 10.1007/BF00451451. Hum Genet. 1988. PMID: 2843456
Autosomal recessive hypophosphataemic rickets with hypercalciuria is not caused by mutations in the type II renal sodium/phosphate cotransporter gene.
van den Heuvel L, Op de Koul K, Knots E, Knoers N, Monnens L. van den Heuvel L, et al. Among authors: monnens l. Nephrol Dial Transplant. 2001 Jan;16(1):48-51. doi: 10.1093/ndt/16.1.48. Nephrol Dial Transplant. 2001. PMID: 11208993
Mutation analysis and clinical implications of von Willebrand factor-cleaving protease deficiency.
Assink K, Schiphorst R, Allford S, Karpman D, Etzioni A, Brichard B, van de Kar N, Monnens L, van den Heuvel L. Assink K, et al. Among authors: monnens l. Kidney Int. 2003 Jun;63(6):1995-9. doi: 10.1046/j.1523-1755.63.6s.1.x. Kidney Int. 2003. PMID: 12753286
Bigenic heterozygosity and the development of steroid-resistant focal segmental glomerulosclerosis.
Löwik M, Levtchenko E, Westra D, Groenen P, Steenbergen E, Weening J, Lilien M, Monnens L, van den Heuvel L. Löwik M, et al. Among authors: monnens l. Nephrol Dial Transplant. 2008 Oct;23(10):3146-51. doi: 10.1093/ndt/gfn208. Epub 2008 Apr 28. Nephrol Dial Transplant. 2008. PMID: 18443213
A missense mutation in factor I (IF) predisposes to atypical haemolytic uraemic syndrome.
Geelen J, van den Dries K, Roos A, van de Kar N, de Kat Angelino C, Klasen I, Monnens L, van den Heuvel L. Geelen J, et al. Among authors: monnens l. Pediatr Nephrol. 2007 Mar;22(3):371-5. doi: 10.1007/s00467-006-0320-2. Epub 2006 Nov 15. Pediatr Nephrol. 2007. PMID: 17106690
Anticardiolipin antibodies in D+ hemolytic uremic syndrome.
te Loo M, van der Velden T, Onland W, van den Heuvel L, Monnens L. te Loo M, et al. Among authors: monnens l. Pediatr Nephrol. 2002 Dec;17(12):1042-6. doi: 10.1007/s00467-002-0965-4. Epub 2002 Nov 1. Pediatr Nephrol. 2002. PMID: 12478355 Clinical Trial.
Severe hypomagnesemia in a neonate with isolated renal magnesium loss.
Meij I, Illy KE, Monnens L. Meij I, et al. Among authors: monnens l. Nephron. 2000 Feb;84(2):198. doi: 10.1159/000045575. Nephron. 2000. PMID: 10657728 No abstract available.
Fungal bezoars as a cause of renal insufficiency in neonates and infants--recommended treatment strategy.
Visser D, Monnens L, Feitz W, Semmekrot B. Visser D, et al. Among authors: monnens l. Clin Nephrol. 1998 Mar;49(3):198-201. Clin Nephrol. 1998. PMID: 9543603 Review.
Three-point linkage analysis using multiple DNA polymorphic markers in families with X-linked nephrogenic diabetes insipidus.
Knoers N, van der Heyden H, van Oost BA, Monnens L, Willems J, Ropers HH. Knoers N, et al. Among authors: monnens l. Genomics. 1989 Apr;4(3):434-7. doi: 10.1016/0888-7543(89)90352-2. Genomics. 1989. PMID: 2714800
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