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21篇 您的检索式:作者名="Weely"
    题名 作者 年代 出处 被引量
1Moving instead of asking? Performance-based tests and BASFI-questionnaire measure different aspects of physical function in ankylosing spondylitis显示文摘Van Weely SF van Denderen JC Steultjens MP 0,,:1
2Ma-rked elevation of plasma chitotriosidase activity:a novel hallmark of Gaucher disease显示文摘Hollak CE Van Weely S Van Oers MH 1994J Clin Invest1994,93,:1
3Orphan drug development across Europe:bottlenecks and opportunities显示文摘Heemstra H E de Vrueh RL van Weely S 2008Drug Diseov Today2008,13,1516:1
4Translation of rare dis- ease research into orphan drug development: disease matters显示文摘Heemstra H E van Weely S Btiller H A 2009DrugDiscov Today2009,14,2324:1
5Marked elevation of plasma ehitotriosidase activity: a novel hallmark of Gaueher disease 显示文摘Hollak C E van Weely S van Oers M H 1994J Clin Invest1994,93,3:1
6Marked elevation of plasma chitotriosidase activity,a novel hallmark of Gaucher disease显示文摘HOLLAK C E M WEELY S VAN OVES M H J 1994J Clin Invest1994,93,:1
7Orphan drug development across Europe: bottlenecks and oppor- tunities显示文摘Heemstra HE de Vrueh RL van Weely S 2008Drug Discovery Today2008,13,1516:1
8Marked elevation of plasma chitotriosidase activity: a novel hallmark of Gaucher disease 显示文摘Hollak CE Weely S Oers MH 1994J Clin Invest1994,93,:1
9Translation of rare disease research into orphan drug development:disease matters 显示文摘Heemstra HE van Weely S Bullet HA 2009Drug Discov Today2009,14,2324:1
10Moving instead of asking? Performance-based tests and BASFI-questionnaire measure different aspects of physical function in ankylosing spondylitis显示文摘van Weely SF van Denderen JC Steultjens MP 2012Arthritis Res Ther2012,14,2:1
11Marked elevation of plasma chitotriosidase activity,a novel hakkmark of Gaucher disease显示文摘HOLLAK C E VAN WEELY S VAN OERS M H 1994J Clin Invest1994,93,:1
12Translation of Rare Disease Research into Orphan Drug Development:Disease Matters显示文摘Heemstra H E van Weely S Büller H A 2009Drug Discovery Today2009,14,23:1
13Does market exclusivity hinder the development of Follow-on Orphan Medicinal Products in Europe?显示文摘Anne E M Brabers Ellen H M Moors Sonja van Weely Remco L A de Vmeh 2011Orphanet journal of rare diseases2011,,6:1
14Translation of rare disease research into orphan drug development:disease matters显示文摘Heemstra H E van Weely S Büller H A 2009Drug Discov Today2009,14,2324:1
15Novel oral treatment of Gaucher’s disease with N -butyldeoxynojirimycin (OGT 918) to decrease substrate biosynthesis显示文摘Timothy Cox Robin Lachmann Carla Hollak Johannes Aerts Sonja van Weely Martin Hrebícek Frances Platt Terry Butters Raymond Dwek Chris Moyses Irene Gow Deborah Elstein Ari Zimran 2000The Lancet2000,,9214:1
16Marked elevation of plasma chitotriosidase activity: a novel hallmark of Gaucher disease显示文摘HOLLAK C E van WEELY S van OERS M H 1994J Clin Invest1994,93,3:1
17The frequency of lysosomal storage diseases in The Netherlands显示文摘B.J.H.M. Poorthuis R.A. Wevers W.J. Kleijer J.E.M. Groener J.G.N. de Jong S. van Weely K.E. Niezen-Koning O.P. van Diggelen 19991999 (1-2)1999,,1:1
18Marked elevation of plasma chitotriosidase acifivity 显示文摘Hollak C E van Weely S van Oers M H 1994J Clin Invest1994,93,:1
19Marked elevation of plasma chitotriosidase acitivity显示文摘Hollak CE van Weely S van Oers MH 0,,03:1
20Translation of rare disease research into orphan drug development:disease matters显示文摘Heemstra H E van Weely S Buller H A 2009Drug Discov Today2009,14,2324:1
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