Müller-Felber W - Search Results

1

Newborn screening for spinal muscular atrophy in Germany: clinical results after 2 years.

Vill K, Schwartz O, Blaschek A, Gläser D, Nennstiel U, Wirth B, Burggraf S, Röschinger W, Becker M, Czibere L, Durner J, Eggermann K, Olgemöller B, Harms E, Schara U, Kölbel H, Müller-Felber W. Vill K, et al. Orphanet J Rare Dis. 2021 Mar 31;16(1):153. doi: 10.1186/s13023-021-01783-8. Orphanet J Rare Dis. 2021. PMID: 33789695 Free PMC article.

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

Somatropin treatment of spinal muscular atrophy: a placebo-controlled, double-blind crossover pilot study.

Kirschner J, Schorling D, Hauschke D, Rensing-Zimmermann C, Wein U, Grieben U, Schottmann G, Schara U, Konrad K, Müller-Felber W, Thiele S, Wilichowski E, Hobbiebrunken E, Stettner GM, Korinthenberg R. Kirschner J, et al. Neuromuscul Disord. 2014 Feb;24(2):134-42. doi: 10.1016/j.nmd.2013.10.011. Epub 2013 Nov 13. Neuromuscul Disord. 2014. PMID: 24300782 Clinical Trial.

7

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

8

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

9

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

10

Diagnostic algorithms in Charcot-Marie-Tooth neuropathies: experiences from a German genetic laboratory on the basis of 1206 index patients.

Rudnik-Schöneborn S, Tölle D, Senderek J, Eggermann K, Elbracht M, Kornak U, von der Hagen M, Kirschner J, Leube B, Müller-Felber W, Schara U, von Au K, Wieczorek D, Bußmann C, Zerres K. Rudnik-Schöneborn S, et al. Clin Genet. 2016 Jan;89(1):34-43. doi: 10.1111/cge.12594. Epub 2015 Apr 29. Clin Genet. 2016. PMID: 25850958

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