Monnens L - Search Results

1

Congenital eyelid ptosis, decreased glomerular filtration, and orthostatic hypotension: Answers.

Wassenberg T, Willemsen M, Dijkman H, Deinum J, Monnens L. Wassenberg T, et al. Among authors: monnens l. Pediatr Nephrol. 2017 Jul;32(7):1171-1174. doi: 10.1007/s00467-016-3515-1. Epub 2016 Nov 17. Pediatr Nephrol. 2017. PMID: 27858196 Free PMC article. No abstract available.

2

The glycosaminoglycan content of renal basement membranes in the congenital nephrotic syndrome of the Finnish type.

Van den Heuvel LP, Van den Born J, Jalanko H, Schröder CH, Veerkamp JH, Assmann KJ, Berden JH, Holmberg C, Rapola J, Monnens LA. Van den Heuvel LP, et al. Among authors: monnens la. Pediatr Nephrol. 1992 Jan;6(1):10-5. doi: 10.1007/BF00856820. Pediatr Nephrol. 1992. PMID: 1536728

3

The development of anti-glomerular basement membrane nephritis in two children with Alport's syndrome after renal transplantation: characterization of the antibody target.

vd Heuvel LP, Schröder CH, Savage CO, Menzel D, Assmann KJ, Monnens LA, Veerkamp JH. vd Heuvel LP, et al. Among authors: monnens la. Pediatr Nephrol. 1989 Oct;3(4):406-13. doi: 10.1007/BF00850217. Pediatr Nephrol. 1989. PMID: 2642109

4

The syndrome of hypertension and hyperkalaemia with normal glomerular function (Gordon's syndrome). A pathophysiological study.

Semmekrot B, Monnens L, Theelen BG, Rascher W, Gabreëls F, Willems J. Semmekrot B, et al. Among authors: monnens l. Pediatr Nephrol. 1987 Jul;1(3):473-8. doi: 10.1007/BF00849256. Pediatr Nephrol. 1987. PMID: 2978968

5

2,8-Dihydroxyadenine stone formation in a renal transplant recipient due to adenine phosphoribosyltransferase deficiency.

de Jong DJ, Assmann KJ, De Abreu RA, Monnens LA, van Liebergen FJ, Dijkman HB, Huysmans FT. de Jong DJ, et al. Among authors: monnens la. J Urol. 1996 Nov;156(5):1754-5. doi: 10.1097/00005392-199611000-00057. J Urol. 1996. PMID: 8863589 No abstract available.

6

Hereditary disorders of the glomerular basement membrane.

Smeets HJ, Knoers VV, van de Heuvel LP, Lemmink HH, Schröder CH, Monnens LA. Smeets HJ, et al. Among authors: monnens la. Pediatr Nephrol. 1996 Dec;10(6):779-88. doi: 10.1007/s004670050217. Pediatr Nephrol. 1996. PMID: 8971907 Review.

7

Evidence for the existence of multiple heparan sulfate proteoglycans in the human glomerular basement membrane and mesangial matrix.

Groffen AJ, Hop FW, Tryggvason K, Dijkman H, Assmann KJ, Veerkamp JH, Monnens LA, Van den Heuvel LP. Groffen AJ, et al. Among authors: monnens la. Eur J Biochem. 1997 Jul 1;247(1):175-82. doi: 10.1111/j.1432-1033.1997.00175.x. Eur J Biochem. 1997. PMID: 9249024 Free article.

8

Agrin is a major heparan sulfate proteoglycan in the human glomerular basement membrane.

Groffen AJ, Ruegg MA, Dijkman H, van de Velden TJ, Buskens CA, van den Born J, Assmann KJ, Monnens LA, Veerkamp JH, van den Heuvel LP. Groffen AJ, et al. Among authors: monnens la. J Histochem Cytochem. 1998 Jan;46(1):19-27. doi: 10.1177/002215549804600104. J Histochem Cytochem. 1998. PMID: 9405491

9

Monocyte chemoattractant protein-1 and interleukin-8 levels in urine and serum of patents with hemolytic uremic syndrome.

van Setten PA, van Hinsbergh VW, van den Heuvel LP, Preyers F, Dijkman HB, Assmann KJ, van der Velden TJ, Monnens LA. van Setten PA, et al. Among authors: monnens la. Pediatr Res. 1998 Jun;43(6):759-67. doi: 10.1203/00006450-199806000-00008. Pediatr Res. 1998. PMID: 9621985

10

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

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