van Engelen BG - Search Results

1

The Dutch patients' perspective on oculopharyngeal muscular dystrophy: A questionnaire study on fatigue, pain and impairments.

van der Sluijs BM, Knoop H, Bleijenberg G, van Engelen BG, Voermans NC. van der Sluijs BM, et al. Among authors: van engelen bg. Neuromuscul Disord. 2016 Mar;26(3):221-6. doi: 10.1016/j.nmd.2015.12.009. Epub 2016 Feb 13. Neuromuscul Disord. 2016. PMID: 26948710

2

A new phenotype of autosomal dominant nemaline myopathy.

Gommans IM, van Engelen BG, ter Laak HJ, Brunner HG, Kremer H, Lammens M, Vogels OJ. Gommans IM, et al. Among authors: van engelen bg. Neuromuscul Disord. 2002 Jan;12(1):13-8. doi: 10.1016/s0960-8966(01)00231-0. Neuromuscul Disord. 2002. PMID: 11731279

3

Oculopharyngeal muscular dystrophy (OPMD) due to a small duplication in the PABPN1 gene.

van der Sluijs BM, van Engelen BG, Hoefsloot LH. van der Sluijs BM, et al. Among authors: van engelen bg. Hum Mutat. 2003 May;21(5):553. doi: 10.1002/humu.9138. Hum Mutat. 2003. PMID: 12673802

4

Oculopharyngeal muscular dystrophy with limb girdle weakness as major complaint.

Van Der Sluijs BM, Hoefsloot LH, Padberg GW, Van Der Maarel SM, Van Engelen BG. Van Der Sluijs BM, et al. Among authors: van der maarel sm, van engelen bg. J Neurol. 2003 Nov;250(11):1307-12. doi: 10.1007/s00415-003-0201-6. J Neurol. 2003. PMID: 14648146

5

[Clinical reasoning and decision making in practice. A 23 year old woman with malaise, anorexia, fever and behavior changes].

Voermans NC, Hart W, van Engelen BG. Voermans NC, et al. Among authors: van engelen bg. Ned Tijdschr Geneeskd. 2004 May 29;148(22):1079-86. Ned Tijdschr Geneeskd. 2004. PMID: 15198060 Dutch.

6

[Fatigue in neuromuscular disease].

Van Engelen BG, Kalkman JS, Schillings ML, Van Der Werf SP, Bleijenberg G, Zwarts MJ. Van Engelen BG, et al. Among authors: van der werf sp. Ned Tijdschr Geneeskd. 2004 Jul 3;148(27):1336-41. Ned Tijdschr Geneeskd. 2004. PMID: 15283024 Review. Dutch.

7

Autosomal recessive oculopharyngodistal myopathy: a distinct phenotypical, histological, and genetic entity.

van der Sluijs BM, ter Laak HJ, Scheffer H, van der Maarel SM, van Engelen BG. van der Sluijs BM, et al. Among authors: van der maarel sm, van engelen bg. J Neurol Neurosurg Psychiatry. 2004 Oct;75(10):1499-501. doi: 10.1136/jnnp.2003.025072. J Neurol Neurosurg Psychiatry. 2004. PMID: 15377709 Free PMC article.

8

Diminished central activation during maximal voluntary contraction in chronic fatigue syndrome.

Schillings ML, Kalkman JS, van der Werf SP, van Engelen BG, Bleijenberg G, Zwarts MJ. Schillings ML, et al. Among authors: van engelen bg, van der werf sp. Clin Neurophysiol. 2004 Nov;115(11):2518-24. doi: 10.1016/j.clinph.2004.06.007. Clin Neurophysiol. 2004. PMID: 15465441

9

123rd ENMC International Workshop: management and therapy in myotonic dystrophy, 6-8 February 2004, Naarden, The Netherlands.

van Engelen BG, Eymard B, Wilcox D. van Engelen BG, et al. Neuromuscul Disord. 2005 May;15(5):389-94. doi: 10.1016/j.nmd.2005.02.001. Neuromuscul Disord. 2005. PMID: 15833434 No abstract available.

10

Statin-disclosed acid maltase deficiency.

Voermans NC, Lammens M, Wevers RA, Hermus AR, van Engelen BG. Voermans NC, et al. Among authors: van engelen bg. J Intern Med. 2005 Aug;258(2):196-7. doi: 10.1111/j.1365-2796.2005.01515.x. J Intern Med. 2005. PMID: 16018797 Free article. No abstract available.

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