van Engelen BGM - Search Results

1

Facioscapulohumeral Dystrophy in Childhood: A Nationwide Natural History Study.

Goselink RJM, Schreuder THA, van Alfen N, de Groot IJM, Jansen M, Lemmers RJLF, van der Vliet PJ, van der Stoep N, Theelen T, Voermans NC, van der Maarel SM, van Engelen BGM, Erasmus CE. Goselink RJM, et al. Among authors: van alfen n, van der maarel sm, van engelen bgm, van der stoep n, van der vliet pj. Ann Neurol. 2018 Nov;84(5):627-637. doi: 10.1002/ana.25326. Epub 2018 Oct 16. Ann Neurol. 2018. PMID: 30179273 Free PMC article.

2

Familial adult-onset muscular dystrophy with leukoencephalopathy.

van Engelen BG, Leyten QH, Bernsen PL, Gabreëls FJ, Barkhof F, Joosten EM, Hamel BC, ter Laak HJ, Ruijs MB, Cruysberg JR, et al. van Engelen BG, et al. Ann Neurol. 1992 Oct;32(4):577-80. doi: 10.1002/ana.410320415. Ann Neurol. 1992. PMID: 1456743

3

Lumbosacral plexus neuropathy: a case report and review of the literature.

van Alfen N, van Engelen BG. van Alfen N, et al. Clin Neurol Neurosurg. 1997 May;99(2):138-41. doi: 10.1016/s0303-8467(97)00603-3. Clin Neurol Neurosurg. 1997. PMID: 9213060 Review.

4

The natural history of hereditary neuralgic amyotrophy in the Dutch population: two distinct types?

van Alfen N, van Engelen BG, Reinders JW, Kremer H, Gabreëls FJ. van Alfen N, et al. Brain. 2000 Apr;123 ( Pt 4):718-23. doi: 10.1093/brain/123.4.718. Brain. 2000. PMID: 10734003

5

Epidemiology of inclusion body myositis in the Netherlands: a nationwide study.

Badrising UA, Maat-Schieman M, van Duinen SG, Breedveld F, van Doorn P, van Engelen B, van den Hoogen F, Hoogendijk J, Höweler C, de Jager A, Jennekens F, Koehler P, van der Leeuw H, de Visser M, Verschuuren JJ, Wintzen AR. Badrising UA, et al. Neurology. 2000 Nov 14;55(9):1385-7. doi: 10.1212/wnl.55.9.1385. Neurology. 2000. PMID: 11087787

6

Idiopathic neuralgic amyotrophy in children. A distinct phenotype compared to the adult form.

van Alfen N, Schuuring J, van Engelen BG, Rotteveel JJ, Gabreëls FJ. van Alfen N, et al. Neuropediatrics. 2000 Dec;31(6):328-32. doi: 10.1055/s-2000-12954. Neuropediatrics. 2000. PMID: 11508556 Review.

7

Llama-derived phage display antibodies in the dissection of the human disease oculopharyngeal muscular dystrophy.

van Koningsbruggen S, de Haard H, de Kievit P, Dirks RW, van Remoortere A, Groot AJ, van Engelen BG, den Dunnen JT, Verrips CT, Frants RR, van der Maarel SM. van Koningsbruggen S, et al. J Immunol Methods. 2003 Aug;279(1-2):149-61. doi: 10.1016/s0022-1759(03)00232-1. J Immunol Methods. 2003. PMID: 12969556

8

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. J Neurol. 2003 Nov;250(11):1307-12. doi: 10.1007/s00415-003-0201-6. J Neurol. 2003. PMID: 14648146

9

[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. Ned Tijdschr Geneeskd. 2004 May 29;148(22):1079-86. Ned Tijdschr Geneeskd. 2004. PMID: 15198060 Dutch.

10

Localization of 4q35.2 to the nuclear periphery: is FSHD a nuclear envelope disease?

Masny PS, Bengtsson U, Chung SA, Martin JH, van Engelen B, van der Maarel SM, Winokur ST. Masny PS, et al. Hum Mol Genet. 2004 Sep 1;13(17):1857-71. doi: 10.1093/hmg/ddh205. Epub 2004 Jul 6. Hum Mol Genet. 2004. PMID: 15238509

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