de Voogt WG - Search Results

1

Cardiac and pulmonary investigations in Bethlem myopathy.

van der Kooi AJ, de Voogt WG, Bertini E, Merlini L, Talim FB, Ben Yaou R, Urtziberea A, de Visser M. van der Kooi AJ, et al. Among authors: de voogt wg, de visser m. Arch Neurol. 2006 Nov;63(11):1617-21. doi: 10.1001/archneur.63.11.1617. Arch Neurol. 2006. PMID: 17101832

2

The heart in Becker muscular dystrophy, facioscapulohumeral dystrophy, and Bethlem myopathy.

de Visser M, de Voogt WG, la Rivière GV. de Visser M, et al. Among authors: de voogt wg. Muscle Nerve. 1992 May;15(5):591-6. doi: 10.1002/mus.880150510. Muscle Nerve. 1992. PMID: 1584251

3

A newly recognized autosomal dominant limb girdle muscular dystrophy with cardiac involvement.

van der Kooi AJ, Ledderhof TM, de Voogt WG, Res CJ, Bouwsma G, Troost D, Busch HF, Becker AE, de Visser M. van der Kooi AJ, et al. Among authors: de voogt wg, de visser m. Ann Neurol. 1996 May;39(5):636-42. doi: 10.1002/ana.410390513. Ann Neurol. 1996. PMID: 8619549 Free article.

4

Cardiac involvement in Dutch patients with sarcoglycanopathy: a cross-sectional cohort and follow-up study.

Schade van Westrum SM, Dekker LR, de Voogt WG, Wilde AA, Ginjaar IB, de Visser M, van der Kooi AJ. Schade van Westrum SM, et al. Among authors: de voogt wg. Muscle Nerve. 2014 Dec;50(6):909-13. doi: 10.1002/mus.24233. Muscle Nerve. 2014. PMID: 24619517

5

Evolution of cardiac abnormalities in Becker muscular dystrophy over a 13-year period.

Hoogerwaard EM, de Voogt WG, Wilde AA, van der Wouw PA, Bakker E, van Ommen GJ, de Visser M. Hoogerwaard EM, et al. Among authors: de voogt wg, de visser m. J Neurol. 1997 Oct;244(10):657-63. doi: 10.1007/s004150050163. J Neurol. 1997. PMID: 9402544 Clinical Trial.

6

The heart in limb girdle muscular dystrophy.

van der Kooi AJ, de Voogt WG, Barth PG, Busch HF, Jennekens FG, Jongen PJ, de Visser M. van der Kooi AJ, et al. Among authors: de voogt wg, de visser m. Heart. 1998 Jan;79(1):73-7. doi: 10.1136/hrt.79.1.73. Heart. 1998. PMID: 9505924 Free PMC article.

7

Long-term follow-up study on patients with Miyoshi phenotype of distal muscular dystrophy.

Linssen WH, de Voogt WG, Krahn M, Bernard R, Levy N, Wokke JH, Ginjaar HB, de Visser M. Linssen WH, et al. Among authors: de voogt wg. Eur J Neurol. 2013 Jun;20(6):968-74. doi: 10.1111/ene.12129. Epub 2013 Mar 26. Eur J Neurol. 2013. PMID: 23530687

8

[The heartache of muscular dystrophy].

Hoogerwaard EM, Ginjaar HB, Wilde AA, Leschot NJ, de Voogt WG, de Visser M. Hoogerwaard EM, et al. Among authors: de voogt wg, de visser m. Ned Tijdschr Geneeskd. 2000 Nov 11;144(46):2181-4. Ned Tijdschr Geneeskd. 2000. PMID: 11103252 Review. Dutch.

9

Meta-analysis of clinical characteristics of 299 carriers of LMNA gene mutations: do lamin A/C mutations portend a high risk of sudden death?

van Berlo JH, de Voogt WG, van der Kooi AJ, van Tintelen JP, Bonne G, Yaou RB, Duboc D, Rossenbacker T, Heidbüchel H, de Visser M, Crijns HJ, Pinto YM. van Berlo JH, et al. Among authors: de voogt wg, de visser m. J Mol Med (Berl). 2005 Jan;83(1):79-83. doi: 10.1007/s00109-004-0589-1. Epub 2004 Nov 13. J Mol Med (Berl). 2005. PMID: 15551023

10

Early prediction of improvement in ejection fraction after acute myocardial infarction using low dose dobutamine echocardiography.

Nijland F, Kamp O, Verhorst PM, de Voogt WG, Visser CA. Nijland F, et al. Among authors: de voogt wg. Heart. 2002 Dec;88(6):592-6. doi: 10.1136/heart.88.6.592. Heart. 2002. PMID: 12433887 Free PMC article.

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