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Browsing by Author Veldink, J.H.

Full Text	Issue Date	Title	Author(s)
	2011	Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis.	Es, M.A. van; Schelhaas, H.J.; Vught, P.W. van; Ticozzi, N.; Andersen, P.M., et al
	2011	Population based epidemiology of amyotrophic lateral sclerosis using capture-recapture methodology	Huisman, M.H.; Jong, S.W. de; Doormaal, P.T. van; Weinreich, S.S.; Schelhaas, H.J., et al
	2011	European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptibility gene	Rafnar, T.; Vermeulen, H.H.M.; Sulem, P.; Thorleifsson, G.; Aben, K.K.H., et al
	2011	Family history of neurodegenerative and vascular diseases in ALS: a population-based study	Huisman, M.H.; Jong, S.W. de; Verwijs, M.C.; Schelhaas, H.J.; Kooi, A.J. van der, et al
	2010	Correlates of outcome and response to IVIg in 88 patients with multifocal motor neuropathy	Cats, E.A.; Pol, W.L. van der; Piepers, S.; Franssen, H.; Jacobs, B.C., et al
	2010	FUS mutations in familial amyotrophic lateral sclerosis in the Netherlands.	Groen, E.J.; Es, M.A. van; Vught, P.W. van; Spliet, W.G.; Engelen-Lee, J. van, et al
	2010	A large genome scan for rare CNVs in amyotrophic lateral sclerosis.	Blauw, H.M.; Al-Chalabi, A.; Andersen, P.M.; Vught, P.W. van; Diekstra, F.P., et al
	2010	Amyotrofische laterale sclerose	Veldink, J.H.; Weikamp, J.G.; Schelhaas, H.J.; Berg, L.H. van den
	2009	Analysis of FGGY as a risk factor for sporadic amyotrophic lateral sclerosis.	Es, M.A. van; Vught, P.W. van; Veldink, J.H.; Andersen, P.M.; Birve, A., et al
	2009	Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.	Es, M.A. van; Veldink, J.H.; Saris, C.G.; Blauw, H.M.; Vught, P.W. van, et al
	2009	A case of ALS-FTD in a large FALS pedigree with a K17I ANG mutation.	Es, M.A. van; Diekstra, F.P.; Veldink, J.H.; Baas, F.; Bourque, P.R., et al
	2009	Differentiation of hereditary spastic paraparesis from primary lateral sclerosis in sporadic adult-onset upper motor neuron syndromes.	Brugman, F.; Veldink, J.H.; Franssen, H.; Visser, M. de; Jong, J.M. de, et al
	2009	Randomized sequential trial of valproic acid in amyotrophic lateral sclerosis.	Piepers, S.; Veldink, J.H.; Jong, S.W. de; Tweel, I. van de; Pol, W.L. van der, et al
	2008	Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis.	Es, M.A. van; Vught, P.W. van; Blauw, H.M.; Franke, L.; Saris, C.G., et al
	2008	Paraplegin mutations in sporadic adult-onset upper motor neuron syndromes.	Brugman, F.; Scheffer, H.; Wokke, J.H.; Nillesen, W.M.; Visser, M. de, et al
	2007	ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study.	Es, M.A. van; Vught, P.W. van; Blauw, H.M.; Franke, L.; Saris, C.G., et al
	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