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

Müller-Felber, Wolfgang ; Vill, Katharina

Neuropediatrics, 2017, Vol.48(04) Neuropediatrics, 2017, Vol.48(04), pp.221-225 [Rivista Peer Reviewed]

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Unilateral Tongue Fasciculation Associated with Genetic Paraganglioma Syndrome

Borggraefe, Ingo ; Mueller-Felber, Wolfgang ; Schmid, Irene ; Huetker, Sebastian

Neuropediatrics, 2018, Vol.49(01) Neuropediatrics, 2017, Vol.49(01), pp.078-079 [Rivista Peer Reviewed]

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Overlap Phenotype between CMT1A and Hereditary Neuropathy with Liability to Pressure Palsies Caused by the Novel Small In-frame Deletion c.407_418del12 in Gene

Vill, Katharina ; Kuhn, Marius ; Gläser, Dieter ; Müller-Felber, Wolfgang

Neuropediatrics, 2014, Vol.46(01) Neuropediatrics, 2015, Vol.46(01), pp.044-048 [Rivista Peer Reviewed]

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

Vill, Katharina ; Kuhn, Marius ; Gläser, Dieter ; Walter, Maggie ; Müller-Felber, Wolfgang

Neuropediatrics, 2015, Vol.46(04) Neuropediatrics, 2015, Vol.46(04), pp.282-286 [Rivista Peer Reviewed]

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P 913. Heterozygous Nonsense Variant in the TCF20 Gene as a Cause of Congenital Myopathy

Vill, Katharina ; Müller-Felber, Wolfgang ; Blaschek, Astrid ; Schröder, Sebastian ; Gläser, Dieter ; Kuhn, Marius ; Meitinger, Thomas ; Wagner, Matias

Neuropediatrics, 2018, Vol.49 Neuropediatrics, 2018, Vol.49, pp.S1-S69 [Rivista Peer Reviewed]

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

Vill, Katharina ; Ille, Lena ; Blaschek, Astrid ; Rawer, Rainer ; Landgraf, Mirjam ; Gerstl, Lucia ; Schroeder, Sebastian ; Müller-Felber, Wolfgang

Neuropediatrics, 2017, Vol.48(06) Neuropediatrics, 2017, Vol.48(06), pp.420-425 [Rivista Peer Reviewed]

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FV 318. Infant Automated Motion Recognition Technology Using RGB-Depth Sensors for Markerless, Rater-Independent Detection of Abnormal Movements in Early Infancy—In a Motion Project

Schröder, Sebastian ; Hesse, Nikolas ; Tacke, Uta ; Weinberger, Raphael ; Schulz, Anne ; Vill, Katharina ; Blaschek, Astrid ; Gerstl, Lucia ; Heinen, Florian ; Bodensteiner, Christoph ; Arens, Michael ; Müller-Felber, Wolfgang

Neuropediatrics, 2018, Vol.49 Neuropediatrics, 2018, Vol.49, pp.S1-S69 [Rivista Peer Reviewed]

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Neuromuscular Disorders in Children

Müller-Felber, Wolfgang

Neuropediatrics, 2019, Vol.50(06) Neuropediatrics, 2019, Vol.50(06), pp.412-412 [Rivista Peer Reviewed]

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PRUNE1 Deficiency: Expanding the Clinical and Genetic Spectrum

Alhaddad, Bader ; Schossig, Anna ; Haack, Tobias ; Kovács-Nagy, Reka ; Braunisch, Matthias ; Makowski, Christine ; Senderek, Jan ; Vill, Katharina ; Müller-Felber, Wolfgang ; Strom, Tim ; Krabichler, Birgit ; Freisinger, Peter ; Deshpande, Charu ; Polster, Tilman ; Wolf, Nicole ; Desguerre, Isabelle ; Wörmann, Friedrich ; Rötig, Agnès ; Ahting, Uwe ; Kopajtich, Robert ; Prokisch, Holger ; Meitinger, Thomas ; Feichtinger, René ; Mayr, Johannes ; Jungbluth, Heinz ; Hubmann, Michael ; Zschocke, Johannes ; Distelmaier, Felix ; Koch, Johannes

Neuropediatrics, 2018, Vol.49(05) Neuropediatrics, 2018, Vol.49(05), pp.330-338 [Rivista Peer Reviewed]

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Is Exercise-Induced Fatigue a Problem in Children with Duchenne Muscular Dystrophy?

Blaschek, Astrid ; Rodrigues, Martin ; Ille, Lena ; Idriess, Mohammed ; Well, Therese ; Warken, Birgit ; Müller, Christine ; Hannibal, Iris ; Tacke, Moritz ; Müller-Felber, Wolfgang ; Vill, Katharina

Neuropediatrics, 2020 [Rivista Peer Reviewed]

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da questo autore/creatore:

  1. Müller-Felber, Wolfgang
  2. Vill, Katharina
  3. Müller-Felber, W.
  4. Vill, K.
  5. Blaschek, Astrid

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