Vill K - Search Results

1

Jumping Mechanography as a Complementary Testing Tool for Motor Function in Children with Hereditary Motor and Sensory Neuropathy.

Vill K, Ille L, Blaschek A, Rawer R, Landgraf MN, Gerstl L, Schroeder SA, Müller-Felber W. Vill K, et al. Neuropediatrics. 2017 Dec;48(6):420-425. doi: 10.1055/s-0037-1603778. Epub 2017 Jun 22. Neuropediatrics. 2017. PMID: 28641335 No abstract available.

2

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. Among authors: vill k. Neuropediatrics. 2013 Dec;44(6):314-23. doi: 10.1055/s-0033-1358600. Epub 2013 Nov 7. Neuropediatrics. 2013. PMID: 24203857 Review.

3

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

4

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

5

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

6

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.

7

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

8

Successful mechanical thrombectomy in a three-year-old boy with cardioembolic occlusion of both the basilar artery and the left middle cerebral artery.

Gerstl L, Olivieri M, Heinen F, Borggraefe I, Schroeder AS, Tacke M, Vill K, Dalla-Pozza R, Reiter K, Lutz J, Brueckmann H, Janssen H. Gerstl L, et al. Among authors: vill k. Eur J Paediatr Neurol. 2016 Nov;20(6):962-965. doi: 10.1016/j.ejpn.2016.07.014. Epub 2016 Jul 25. Eur J Paediatr Neurol. 2016. PMID: 27477566

9

A homozygous splice variant in AP4S1 mimicking neurodegeneration with brain iron accumulation.

Vill K, Müller-Felber W, Alhaddad B, Strom TM, Teusch V, Weigand H, Blaschek A, Meitinger T, Haack TB. Vill K, et al. Mov Disord. 2017 May;32(5):797-799. doi: 10.1002/mds.26922. Epub 2017 Feb 2. Mov Disord. 2017. PMID: 28150420 No abstract available.

10

Clinical Neurophysiology in Neuromuscular Disorders: Old Fashioned or Still Relevant?

Müller-Felber W, Vill K. Müller-Felber W, et al. Among authors: vill k. Neuropediatrics. 2017 Aug;48(4):221-225. doi: 10.1055/s-0037-1603777. Epub 2017 Jun 19. Neuropediatrics. 2017. PMID: 28628940 Review. No abstract available.

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