N A M E van der Beek
Overview
Explore the profile of N A M E van der Beek including associated specialties, affiliations and a list of published articles.
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15
Citations
338
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Recent Articles
11.
van der Beek N, Hagemans M, Reuser A, Hop W, van der Ploeg A, van Doorn P, et al.
Neuromuscul Disord
. 2008 Dec;
19(2):113-7.
PMID: 19084399
To determine the rate of disease progression in patients with late-onset Pompe disease, we collected longitudinal data on pulmonary function and skeletal muscle strength in 16 patients whose symptoms had...
12.
van der Beek N, Soliman O, van Capelle C, Geleijnse M, Vletter W, Kroos M, et al.
J Neurol Sci
. 2008 Sep;
275(1-2):46-50.
PMID: 18757064
Background And Objective: Pompe disease is an inherited metabolic disorder caused by deficiency of acid alpha-glucosidase. All affected neonates have a severe hypertrophic cardiomyopathy, leading to cardiac failure and death...
13.
Soliman O, van der Beek N, van Doorn P, Vletter W, Nemes A, van Dalen B, et al.
J Intern Med
. 2008 Apr;
264(4):333-9.
PMID: 18397245
Background: Glycogen storage disease type II or Pompe disease is a neuromuscular disorder caused by deficiency of lysosomal acid alpha- glucosidase. Classic infantile Pompe disease results in massive left ventricular...
14.
Kroos M, Pomponio R, Hagemans M, Keulemans J, Phipps M, DeRiso M, et al.
Neurology
. 2007 Jan;
68(2):110-5.
PMID: 17210890
Background: Pompe disease (acid maltase deficiency, glycogen storage disease type II; OMIM 232300) is an autosomal recessive lysosomal storage disorder characterized by acid alpha-glucosidase deficiency due to mutations in the...
15.
van der Beek N, Hagemans M, van der Ploeg A, Reuser A, van Doorn P
Acta Neurol Belg
. 2006 Aug;
106(2):82-6.
PMID: 16898258
Pompe disease (glycogen storage disease type II, acid maltase deficiency) is a progressive metabolic myopathy caused by deficiency of the lysosomal enzyme acid alpha-glucosidase. This leads to an accumulation of...