Van Engelen BG - Search Results

1

Brody Disease, an Early-Onset Myopathy With Delayed Relaxation and Abnormal Gait: A Case Series of 9 Children.

Verhoeven JI, Kramer J, Seeger J, Molenaar JP, Braakman H, Kamsteeg EJ, Rodenburg RJ, Kusters B, Koudijs S, Van Engelen BG, Erasmus CE, Voermans NC. Verhoeven JI, et al. Among authors: van engelen bg. Neurology. 2024 Mar 12;102(5):e209164. doi: 10.1212/WNL.0000000000209164. Epub 2024 Feb 19. Neurology. 2024. PMID: 38373275

2

[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.

3

The effect of dantrolene sodium in Very Long Chain Acyl-CoA Dehydrogenase Deficiency.

Voermans NC, Poels PJ, Kluijtmans LA, van Engelen BG. Voermans NC, et al. Among authors: van engelen bg. Neuromuscul Disord. 2005 Dec;15(12):844-6. doi: 10.1016/j.nmd.2005.09.003. Epub 2005 Nov 8. Neuromuscul Disord. 2005. PMID: 16288870

4

Recurrent neuropathy associated with Ehlers-Danlos syndrome.

Voermans NC, Drost G, van Kampen A, Gabreëls-Festen AA, Lammens M, Hamel BC, Schalkwijk J, van Engelen BG. Voermans NC, et al. Among authors: van kampen a, van engelen bg. J Neurol. 2006 May;253(5):670-1. doi: 10.1007/s00415-005-0056-0. Epub 2005 Nov 29. J Neurol. 2006. PMID: 16311893 No abstract available.

5

Rhabdomyolysis caused by an inherited metabolic disease: very long-chain acyl-CoA dehydrogenase deficiency.

Voermans NC, van Engelen BG, Kluijtmans LA, Stikkelbroeck NM, Hermus AR. Voermans NC, et al. Among authors: van engelen bg. Am J Med. 2006 Feb;119(2):176-9. doi: 10.1016/j.amjmed.2005.07.064. Am J Med. 2006. PMID: 16443431 No abstract available.

6

Measurement of the energy-generating capacity of human muscle mitochondria: diagnostic procedure and application to human pathology.

Janssen AJ, Trijbels FJ, Sengers RC, Wintjes LT, Ruitenbeek W, Smeitink JA, Morava E, van Engelen BG, van den Heuvel LP, Rodenburg RJ. Janssen AJ, et al. Among authors: van engelen bg, van den heuvel lp. Clin Chem. 2006 May;52(5):860-71. doi: 10.1373/clinchem.2005.062414. Epub 2006 Mar 16. Clin Chem. 2006. PMID: 16543390 Free article.

7

The mitochondrial 13513G > A mutation is most frequent in Leigh syndrome combined with reduced complex I activity, optic atrophy and/or Wolff-Parkinson-White.

Ruiter EM, Siers MH, van den Elzen C, van Engelen BG, Smeitink JA, Rodenburg RJ, Hol FA. Ruiter EM, et al. Among authors: van engelen bg, van den elzen c. Eur J Hum Genet. 2007 Feb;15(2):155-61. doi: 10.1038/sj.ejhg.5201735. Epub 2006 Nov 15. Eur J Hum Genet. 2007. PMID: 17106447

8

Reduced quantitative muscle function in tenascin-X deficient Ehlers-Danlos patients.

Voermans NC, Altenburg TM, Hamel BC, de Haan A, van Engelen BG. Voermans NC, et al. Among authors: van engelen bg. Neuromuscul Disord. 2007 Aug;17(8):597-602. doi: 10.1016/j.nmd.2007.04.004. Epub 2007 Jun 27. Neuromuscul Disord. 2007. PMID: 17588758

9

Caffeine and muscle cramps: a stimulating connection.

Molema MM, Dekker MC, Voermans NC, van Engelen BG, Aarnoutse RE. Molema MM, et al. Among authors: van engelen bg. Am J Med. 2007 Aug;120(8):e1-2. doi: 10.1016/j.amjmed.2006.07.035. Am J Med. 2007. PMID: 17679106 Clinical Trial. No abstract available.

10

Chronic progressive external ophthalmoplegia caused by an m.4267A > G mutation in the mitochondrial tRNAIle.

Smits BW, Hol FA, van den Heuvel LP, Drost G, Rodenburg RJ, Ter Laak HJ, van Engelen BG. Smits BW, et al. Among authors: van den heuvel lp, van engelen bg. J Neurol. 2007 Nov;254(11):1614-5. doi: 10.1007/s00415-007-0608-6. Epub 2007 Nov 2. J Neurol. 2007. PMID: 17965958 No abstract available.

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