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Browsing by Author Schwartz, M.

Full Text	Issue Date	Title	Author(s)
	2012	Best practice guidelines and recommendations on the molecular diagnosis of myotonic dystrophy types 1 and 2	Kamsteeg, E.J.; Kress, W.; Catalli, C.; Hertz, J.M.; Witsch-Baumgartner, M., et al
	2010	Barriers to the implementation of traffic calming in Israeli towns and cities and ways to overcome them	Rofé, Y.; Schwartz, M.; Garb, Y.; Martens, C.J.C.M.; Meged-Doron, E., et al
	2008	Barriers to the implementation of traffic calming in Israeli towns and cities and ways to overcome them (in Hebrew)	Rofe, Y.; Aschak, R.; Garb, Y.; Klieger, I.; Martens, C.J.C.M., et al
	2008	Heparanase induces a differential loss of heparan sulphate domains in overt diabetic nephropathy.	Wijnhoven, T.J.; Hoven, M.J.W. van den; Ding, H.; Kuppevelt, A.H.M.S.M. van; Vlag, J. van der, et al
	1997	Molecular basis of choroideremia (CHM): mutations involving the Rab escort protein-1 (REP-1) gene	Hurk, J.A.J.M. van den; Schwartz, M.; Bokhoven, H. van; Pol, T.J.R. van de; Bogerd, L., et al