Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

77 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Home-Based Infusion of Alglucosidase Alfa Can Safely be Implemented in Adults with Late-Onset Pompe Disease: Lessons Learned from 18,380 Infusions.
Ditters IAM, van Kooten HA, van der Beek NAME, Hardon JF, Ismailova G, Brusse E, Kruijshaar ME, van der Ploeg AT, van den Hout JMP, Huidekoper HH. Ditters IAM, et al. Among authors: brusse e. BioDrugs. 2023 Sep;37(5):685-698. doi: 10.1007/s40259-023-00609-2. Epub 2023 Jun 16. BioDrugs. 2023. PMID: 37326923 Free PMC article.
Autosomal recessive spinocerebellar ataxia 7 (SCAR7) is caused by variants in TPP1, the gene involved in classic late-infantile neuronal ceroid lipofuscinosis 2 disease (CLN2 disease).
Sun Y, Almomani R, Breedveld GJ, Santen GW, Aten E, Lefeber DJ, Hoff JI, Brusse E, Verheijen FW, Verdijk RM, Kriek M, Oostra B, Breuning MH, Losekoot M, den Dunnen JT, van de Warrenburg BP, Maat-Kievit AJ. Sun Y, et al. Among authors: brusse e. Hum Mutat. 2013 May;34(5):706-13. doi: 10.1002/humu.22292. Epub 2013 Mar 11. Hum Mutat. 2013. PMID: 23418007
Assessment of disability in idiopathic inflammatory myopathy: a call for linearity.
Min M, Walter AW, Lim J, Eftimov F, Verhamme C, de Visser M, van Schaik IN, Aggarwal R, de Haan RJ, van der Kooi AJ, Raaphorst J; Dutch Myositis Network. Min M, et al. Rheumatology (Oxford). 2022 Aug 3;61(8):3420-3426. doi: 10.1093/rheumatology/keab906. Rheumatology (Oxford). 2022. PMID: 34875011 Free PMC article.
Extension of the clinical spectrum of Danon disease.
van der Kooi AJ, van Langen IM, Aronica E, van Doorn PA, Wokke JH, Brusse E, Langerhorst CT, Bergin P, Dekker LR, dit Deprez RH, de Visser M. van der Kooi AJ, et al. Among authors: brusse e. Neurology. 2008 Apr 15;70(16):1358-9. doi: 10.1212/01.wnl.0000309219.61785.b3. Neurology. 2008. PMID: 18413590 No abstract available.
Pulsed high-dose dexamethasone versus standard prednisolone treatment for chronic inflammatory demyelinating polyradiculoneuropathy (PREDICT study): a double-blind, randomised, controlled trial.
van Schaik IN, Eftimov F, van Doorn PA, Brusse E, van den Berg LH, van der Pol WL, Faber CG, van Oostrom JC, Vogels OJ, Hadden RD, Kleine BU, van Norden AG, Verschuuren JJ, Dijkgraaf MG, Vermeulen M. van Schaik IN, et al. Among authors: brusse e. Lancet Neurol. 2010 Mar;9(3):245-53. doi: 10.1016/S1474-4422(10)70021-1. Epub 2010 Feb 2. Lancet Neurol. 2010. PMID: 20133204 Clinical Trial.
Enzyme replacement therapy and fatigue in adults with Pompe disease.
Güngör D, de Vries JM, Brusse E, Kruijshaar ME, Hop WC, Murawska M, van den Berg LE, Reuser AJ, van Doorn PA, Hagemans ML, Plug I, van der Ploeg AT. Güngör D, et al. Among authors: brusse e. Mol Genet Metab. 2013 Jun;109(2):174-8. doi: 10.1016/j.ymgme.2013.03.016. Epub 2013 Apr 3. Mol Genet Metab. 2013. PMID: 23603069 Free article.
Phenotypical variation within 22 families with Pompe disease.
Wens SC, van Gelder CM, Kruijshaar ME, de Vries JM, van der Beek NA, Reuser AJ, van Doorn PA, van der Ploeg AT, Brusse E. Wens SC, et al. Among authors: brusse e. Orphanet J Rare Dis. 2013 Nov 19;8:182. doi: 10.1186/1750-1172-8-182. Orphanet J Rare Dis. 2013. PMID: 24245577 Free PMC article.
77 results