Voermans NC - Search Results

1

Experiences with bariatric surgery in patients with facioscapulohumeral dystrophy and myotonic dystrophy type 1: A qualitative study.

Abel EEDH, Cup EHC, Lanser A, Leclercq WKG, Raaphorst J, Padberg GW, Satink T, Voermans NC. Abel EEDH, et al. Among authors: voermans nc. Neuromuscul Disord. 2018 Nov;28(11):938-946. doi: 10.1016/j.nmd.2018.09.003. Epub 2018 Sep 19. Neuromuscul Disord. 2018. PMID: 30342904

2

Sarcomeric dysfunction contributes to muscle weakness in facioscapulohumeral muscular dystrophy.

Lassche S, Stienen GJ, Irving TC, van der Maarel SM, Voermans NC, Padberg GW, Granzier H, van Engelen BG, Ottenheijm CA. Lassche S, et al. Among authors: voermans nc. Neurology. 2013 Feb 19;80(8):733-7. doi: 10.1212/WNL.0b013e318282513b. Epub 2013 Jan 30. Neurology. 2013. PMID: 23365058 Free PMC article.

3

Determining the role of sarcomeric proteins in facioscapulohumeral muscular dystrophy: a study protocol.

Lassche S, Ottenheijm CA, Voermans NC, Westeneng HJ, Janssen BH, van der Maarel SM, Hopman MT, Padberg GW, Stienen GJ, van Engelen BG. Lassche S, et al. Among authors: voermans nc. BMC Neurol. 2013 Oct 11;13:144. doi: 10.1186/1471-2377-13-144. BMC Neurol. 2013. PMID: 24119284 Free PMC article.

4

Compound heterozygous mutations of the TNXB gene cause primary myopathy.

Voermans NC, Gerrits K, van Engelen BG, de Haan A. Voermans NC, et al. Neuromuscul Disord. 2014 Jan;24(1):88-9. doi: 10.1016/j.nmd.2013.10.007. Epub 2013 Nov 5. Neuromuscul Disord. 2014. PMID: 24300784 No abstract available.

5

High prevalence of incomplete right bundle branch block in facioscapulohumeral muscular dystrophy without cardiac symptoms.

van Dijk GP, van der Kooi E, Behin A, Smeets J, Timmermans J, van der Maarel S, Padberg G, Voermans N, van Engelen B. van Dijk GP, et al. Funct Neurol. 2014 Jul-Sep;29(3):159-65. Funct Neurol. 2014. PMID: 25473735 Free PMC article.

6

Primary cataract as a key to recognition of myotonic dystrophy type 1.

Voermans NC, Erasmus CE, Ockeloen CW, Van Engelen BG, Eggink CA. Voermans NC, et al. Eur J Ophthalmol. 2015 May 25;25(4):e46-9. doi: 10.5301/ejo.5000565. Eur J Ophthalmol. 2015. PMID: 25655594

7

Facioscapulohumeral muscular dystrophy as a genetic cause of pectus excavatum.

Mul K, Padberg GW, Voermans NC. Mul K, et al. Among authors: voermans nc. Eur J Med Genet. 2015 Apr;58(4):203-4. doi: 10.1016/j.ejmg.2015.02.007. Epub 2015 Feb 25. Eur J Med Genet. 2015. PMID: 25725206 No abstract available.

8

What's in a name? The clinical features of facioscapulohumeral muscular dystrophy.

Mul K, Lassche S, Voermans NC, Padberg GW, Horlings CG, van Engelen BG. Mul K, et al. Among authors: voermans nc. Pract Neurol. 2016 Jun;16(3):201-7. doi: 10.1136/practneurol-2015-001353. Epub 2016 Feb 9. Pract Neurol. 2016. PMID: 26862222 Review.

9

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: voermans nc. 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

10

Facioscapulohumeral dystrophy in children: design of a prospective, observational study on natural history, predictors and clinical impact (iFocus FSHD).

Goselink RJ, Schreuder TH, Mul K, Voermans NC, Pelsma M, de Groot IJ, van Alfen N, Franck B, Theelen T, Lemmers RJ, Mah JK, van der Maarel SM, van Engelen BG, Erasmus CE. Goselink RJ, et al. Among authors: voermans nc. BMC Neurol. 2016 Aug 17;16:138. doi: 10.1186/s12883-016-0664-6. BMC Neurol. 2016. PMID: 27530735 Free PMC article. Clinical Trial.

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