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Value of plasma chitotriosidase to assess non-neuronopathic Gaucher disease severity and progression in the era of enzyme replacement therapy.
van Dussen L, Hendriks EJ, Groener JE, Boot RG, Hollak CE, Aerts JM. van Dussen L, et al. J Inherit Metab Dis. 2014 Nov;37(6):991-1001. doi: 10.1007/s10545-014-9711-x. Epub 2014 May 16. J Inherit Metab Dis. 2014. PMID: 24831585
Modelling Gaucher disease progression: long-term enzyme replacement therapy reduces the incidence of splenectomy and bone complications.
van Dussen L, Biegstraaten M, Dijkgraaf MG, Hollak CE. van Dussen L, et al. Orphanet J Rare Dis. 2014 Jul 24;9:112. doi: 10.1186/s13023-014-0112-x. Orphanet J Rare Dis. 2014. PMID: 25056340 Free PMC article.
Lung Transplantation in Gaucher Disease: A Learning Lesson in Trying to Avoid Both Scylla and Charybdis.
de Boer GM, van Dussen L, van den Toorn LM, den Bakker MA, Hoek RA, Hesselink DA, Hollak CE, van Hal PT. de Boer GM, et al. Among authors: van dussen l. Chest. 2016 Jan;149(1):e1-5. doi: 10.1016/j.chest.2015.09.011. Epub 2016 Jan 6. Chest. 2016. PMID: 26757299
Hepatocellular carcinoma in Gaucher disease: an international case series.
Regenboog M, van Dussen L, Verheij J, Weinreb NJ, Santosa D, Vom Dahl S, Häussinger D, Müller MN, Canbay A, Rigoldi M, Piperno A, Dinur T, Zimran A, Mistry PK, Salah KY, Belmatoug N, Kuter DJ, Hollak CEM. Regenboog M, et al. Among authors: van dussen l. J Inherit Metab Dis. 2018 Sep;41(5):819-827. doi: 10.1007/s10545-018-0142-y. Epub 2018 Feb 8. J Inherit Metab Dis. 2018. PMID: 29423829 Free PMC article. Clinical Trial.
Cost-effectiveness of enzyme replacement therapy for type 1 Gaucher disease.
van Dussen L, Biegstraaten M, Hollak CE, Dijkgraaf MG. van Dussen L, et al. Orphanet J Rare Dis. 2014 Apr 14;9:51. doi: 10.1186/1750-1172-9-51. Orphanet J Rare Dis. 2014. PMID: 24731506 Free PMC article.
Liver fibrosis in type I Gaucher disease: magnetic resonance imaging, transient elastography and parameters of iron storage.
Bohte AE, van Dussen L, Akkerman EM, Nederveen AJ, Sinkus R, Jansen PL, Stoker J, Hollak CE. Bohte AE, et al. Among authors: van dussen l. PLoS One. 2013;8(3):e57507. doi: 10.1371/journal.pone.0057507. Epub 2013 Mar 15. PLoS One. 2013. PMID: 23554863 Free PMC article. Clinical Trial.
Effects of switching from a reduced dose imiglucerase to velaglucerase in type 1 Gaucher disease: clinical and biochemical outcomes.
van Dussen L, Cox TM, Hendriks EJ, Morris E, Akkerman EM, Maas M, Groener JE, Aerts JM, Deegan PB, Hollak CE. van Dussen L, et al. Haematologica. 2012 Dec;97(12):1850-4. doi: 10.3324/haematol.2011.059071. Epub 2012 Jul 6. Haematologica. 2012. PMID: 22773601 Free PMC article.
Characteristics of type I Gaucher disease associated with persistent thrombocytopenia after treatment with imiglucerase for 4-5 years.
Hollak CE, Belmatoug N, Cole JA, Vom Dahl S, Deegan PB, Goldblatt J, Rosenbloom B, van Dussen L, Tylki-Szymańska A, Weinreb NJ, Zimran A, Cappellini MD. Hollak CE, et al. Among authors: van dussen l. Br J Haematol. 2012 Aug;158(4):528-38. doi: 10.1111/j.1365-2141.2012.09175.x. Epub 2012 May 29. Br J Haematol. 2012. PMID: 22640238 Clinical Trial.
These patients were stratified by last platelet count: ≥ 120 × 10(9) /l (n = 772); ≥ 100 to <120 × 10(9) /l (n = 94); ≥ 80 to <100 × 10(9) /l (n = 80); and <80 × 10(9) /l (n = 70; 20 with <60 × 10(9) /l) and characterized by initial …
These patients were stratified by last platelet count: ≥ 120 × 10(9) /l (n = 772); ≥ 100 to <120 × 10(9) /l (n = 94); ≥ 80 …
Elevated plasma glucosylsphingosine in Gaucher disease: relation to phenotype, storage cell markers, and therapeutic response.
Dekker N, van Dussen L, Hollak CE, Overkleeft H, Scheij S, Ghauharali K, van Breemen MJ, Ferraz MJ, Groener JE, Maas M, Wijburg FA, Speijer D, Tylki-Szymanska A, Mistry PK, Boot RG, Aerts JM. Dekker N, et al. Among authors: van dussen l, van breemen mj. Blood. 2011 Oct 20;118(16):e118-27. doi: 10.1182/blood-2011-05-352971. Epub 2011 Aug 25. Blood. 2011. PMID: 21868580 Free PMC article.
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