Müller-Felber W - Search Results

1

Six-minute walk test versus two-minute walk test in children with Duchenne muscular dystrophy: Is more time more information?

Vill K, Ille L, Schroeder SA, Blaschek A, Müller-Felber W. Vill K, et al. Eur J Paediatr Neurol. 2015 Nov;19(6):640-6. doi: 10.1016/j.ejpn.2015.08.002. Epub 2015 Aug 20. Eur J Paediatr Neurol. 2015. PMID: 26455815 Clinical Trial.

2

Myofascial trigger points in children with tension-type headache: a new diagnostic and therapeutic option.

von Stülpnagel C, Reilich P, Straube A, Schäfer J, Blaschek A, Lee SH, Müller-Felber W, Henschel V, Mansmann U, Heinen F. von Stülpnagel C, et al. J Child Neurol. 2009 Apr;24(4):406-9. doi: 10.1177/0883073808324540. J Child Neurol. 2009. PMID: 19339283 Free article. Clinical Trial.

3

Early white matter changes in childhood multiple sclerosis: a diffusion tensor imaging study.

Blaschek A, Keeser D, Müller S, Koerte IK, Sebastian Schröder A, Müller-Felber W, Heinen F, Ertl-Wagner B. Blaschek A, et al. AJNR Am J Neuroradiol. 2013 Oct;34(10):2015-20. doi: 10.3174/ajnr.A3581. Epub 2013 May 16. AJNR Am J Neuroradiol. 2013. PMID: 23681354 Free PMC article.

4

Salbutamol-responsive limb-girdle congenital myasthenic syndrome due to a novel missense mutation and heteroallelic deletion in MUSK.

Gallenmüller C, Müller-Felber W, Dusl M, Stucka R, Guergueltcheva V, Blaschek A, von der Hagen M, Huebner A, Müller JS, Lochmüller H, Abicht A. Gallenmüller C, et al. Neuromuscul Disord. 2014 Jan;24(1):31-5. doi: 10.1016/j.nmd.2013.08.002. Epub 2013 Aug 7. Neuromuscul Disord. 2014. PMID: 24183479 Free PMC article.

5

Pediatric idiopathic inflammatory myopathies: an update on diagnostic and treatment strategies.

Muller-Felber W, Wanschitz J, Vill K, Baumann M. Muller-Felber W, et al. Neuropediatrics. 2013 Dec;44(6):314-23. doi: 10.1055/s-0033-1358600. Epub 2013 Nov 7. Neuropediatrics. 2013. PMID: 24203857 Review.

6

Early infantile sensory-motor neuropathy with late onset respiratory distress.

Blaschek A, Gläser D, Kuhn M, Schroeder AS, Wimmer C, Heimkes B, Schön C, Müller-Felber W. Blaschek A, et al. Neuromuscul Disord. 2014 Mar;24(3):269-71. doi: 10.1016/j.nmd.2013.11.013. Epub 2013 Dec 1. Neuromuscul Disord. 2014. PMID: 24342282

7

Overlap phenotype between CMT1A and hereditary neuropathy with liability to pressure palsies caused by the novel small in-frame deletion c.407_418del12 in PMP22 gene.

Vill K, Kuhn M, Gläser D, Müller-Felber W. Vill K, et al. Neuropediatrics. 2015 Feb;46(1):44-8. doi: 10.1055/s-0034-1389897. Epub 2014 Sep 29. Neuropediatrics. 2015. PMID: 25265422

8

Muscle ultrasound in classic infantile and adult Pompe disease: a useful screening tool in adults but not in infants.

Vill K, Schessl J, Teusch V, Schroeder S, Blaschek A, Schoser B, Müller-Felber W. Vill K, et al. Neuromuscul Disord. 2015 Feb;25(2):120-6. doi: 10.1016/j.nmd.2014.09.016. Epub 2014 Oct 22. Neuromuscul Disord. 2015. PMID: 25455803

9

Long-Term Observations in an Affected Family with Neurogenic Scapuloperoneal Syndrome Caused by Mutation R269C in the TRPV4 Gene.

Vill K, Kuhn M, Gläser D, Walter MC, Müller-Felber W. Vill K, et al. Neuropediatrics. 2015 Aug;46(4):282-6. doi: 10.1055/s-0035-1554100. Epub 2015 Jun 25. Neuropediatrics. 2015. PMID: 26110311

10

Proximal muscular atrophy and weakness: An unusual adverse effect of deferasirox iron chelation therapy.

Vill K, Müller-Felber W, Teusch V, Blaschek A, Gerstl L, Huetker S, Albert MH. Vill K, et al. Neuromuscul Disord. 2016 Apr-May;26(4-5):322-5. doi: 10.1016/j.nmd.2016.02.011. Epub 2016 Feb 23. Neuromuscul Disord. 2016. PMID: 27068298

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