Müller-Felber W - Search Results

1

Determinants of Plasma Docosahexaenoic Acid Levels and Their Relationship to Neurological and Cognitive Functions in PKU Patients: A Double Blind Randomized Supplementation Study.

Demmelmair H, MacDonald A, Kotzaeridou U, Burgard P, Gonzalez-Lamuno D, Verduci E, Ersoy M, Gokcay G, Alyanak B, Reischl E, Müller-Felber W, Faber FL, Handel U, Paci S, Koletzko B. Demmelmair H, et al. Nutrients. 2018 Dec 7;10(12):1944. doi: 10.3390/nu10121944. Nutrients. 2018. PMID: 30544518 Free PMC article. Clinical Trial.

2

Does dietary DHA improve neural function in children? Observations in phenylketonuria.

Koletzko B, Beblo S, Demmelmair H, Müller-Felber W, Hanebutt FL. Koletzko B, et al. Prostaglandins Leukot Essent Fatty Acids. 2009 Aug-Sep;81(2-3):159-64. doi: 10.1016/j.plefa.2009.06.006. Epub 2009 Jul 16. Prostaglandins Leukot Essent Fatty Acids. 2009. PMID: 19615874

3

Creatine monohydrate in myotonic dystrophy: a double-blind, placebo-controlled clinical study.

Walter MC, Reilich P, Lochmüller H, Kohnen R, Schlotter B, Hautmann H, Dunkl E, Pongratz D, Müller-Felber W. Walter MC, et al. J Neurol. 2002 Dec;249(12):1717-22. doi: 10.1007/s00415-002-0923-x. J Neurol. 2002. PMID: 12529796 Clinical Trial.

4

Creatine monohydrate in muscular dystrophies: A double-blind, placebo-controlled clinical study.

Walter MC, Lochmüller H, Reilich P, Klopstock T, Huber R, Hartard M, Hennig M, Pongratz D, Müller-Felber W. Walter MC, et al. Neurology. 2000 May 9;54(9):1848-50. doi: 10.1212/wnl.54.9.1848. Neurology. 2000. PMID: 10802796 Clinical Trial.

5

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.

6

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

Müller-Felber W, Vill K. Müller-Felber W, et al. 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.

7

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.

8

Spinal Muscular Atrophy - Is Newborn Screening Too Late for Children with Two SMN2 Copies?

Schwartz O, Kölbel H, Blaschek A, Gläser D, Burggraf S, Röschinger W, Schara U, Müller-Felber W, Vill K. Schwartz O, et al. J Neuromuscul Dis. 2022;9(3):389-396. doi: 10.3233/JND-220789. J Neuromuscul Dis. 2022. PMID: 35431259

9

Are evoked potentials in patients with adult-onset pompe disease indicative of clinically relevant central nervous system involvement?

Wirsching A, Müller-Felber W, Schoser B. Wirsching A, et al. J Clin Neurophysiol. 2014 Aug;31(4):362-6. doi: 10.1097/WNP.0000000000000084. J Clin Neurophysiol. 2014. PMID: 25083849

10

High-dose immunoglobulin therapy in sporadic inclusion body myositis: a double-blind, placebo-controlled study.

Walter MC, Lochmüller H, Toepfer M, Schlotter B, Reilich P, Schröder M, Müller-Felber W, Pongratz D. Walter MC, et al. J Neurol. 2000 Jan;247(1):22-8. doi: 10.1007/s004150050005. J Neurol. 2000. PMID: 10701893 Clinical Trial.

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