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Browsing by Author Lemmink, H.H.

Full Text	Issue Date	Title	Author(s)
	2005	SMN genotypes producing less SMN protein increase susceptibility to and severity of sporadic ALS.	Veldink, J.H.; Kalmijn, S.; Hout, A.H. van der; Lemmink, H.H.; Groeneveld, G.J., et al
	1997	Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Barrter syndrome : evidence for genetic heterogeneity	Károlyi, L.; Konrad, M.; Köckerling, A.; Ziegler, A.; Zimmermann, D.K., et al
	1997	Autosomal dominant Alport syndrome linked to the type IV collagen alpha3 and alpha4 genes	Jefferson, J.A.; Lemmink, H.H.; Hughes, A.E.; Hill, C.M.; Smeets, H.J.M., et al
	1997	Functional analysis of ROMK gene mutations in antenatal Bartter syndrome	Lemmink, H.H.; Heuvel, L.P.W.J. van den; Buskens, C.; Kansen, M.; Kemp, A. van der, et al
	1997	Mutation in mitochondrial tRNA (Leu(UUR) gene associated with progressive kidney disease	Jansen, J.J.M.; Maassen, J.A.; Woude, F. van der; Lemmink, H.H.; Ouweland, J.M.W. van den, et al
	1997	The clinical spectrum of type IV collagen mutations	Lemmink, H.H.; Schröder, C.H.; Monnens, L.A.H.; Smeets, H.J.M.
	1996	Linkage of Gitelman syndrome to the thiazide-sensitive sodium-chloride cotransporter gene and identification of mutations in Dutch families	Lemmink, H.H.; Heuvel, L.P.W.J. van den; Dijk, H.A. van; Merkx, G.F.M.; Smilde, T.J., et al
	1996	Benign familial hematuria due to mutation of the type IV collagen alpha-4 gene	Lemmink, H.H.; Nillesen, W.N.; Mochizuki, T.; Schröder, C.H.; Brunner, H.G., et al
	1996	Linkage of Gitelman syndrome to the thiazide-sensitive sodium-chloride cotransporter gene with identification of mutations in Dutch families	Lemmink, H.H.; Heuvel, L.P.W.J. van den; Dijk, H.A. van; Merkx, G.F.M.; Smilde, T.J., et al
	1996	Hereditary disorders of the glomerular basement membrane	Smeets, H.J.M.; Knoers, N.V.A.M.; Heuvel, L.P.W.J. van den; Lemmink, H.H.; Schröder, C.H., et al
	1996	Mutational analyses in Gitelman syndrome	Heuvel, L.P.W.J. van den; Lemmink, H.H.; Tachner, P.E.M.; Vargas, R.; Niaudet, P., et al
	1995	Nieuwe ontwikkelingen in de diagnostiek van het syndroom van Alport	Schröder, C.H.; Lemmink, H.H.; Heuvel, L.P.W.J. van den; Smeets, H.J.M.
	1995	A COL4A3 gene mutation and post-transplant anti-α3(IV) collagen alloantibodies in Alport syndrome	Kalluri, R.; Heuvel, L.P. van den; Smeets, H.J.M.; Schroder, C.H.; Lemmink, H.H., et al