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Pediatric Guillain-Barré Syndrome: Is a low amplitude of nerve action potentials always a bad omen?

Müller-Felber, Wolfgang

European Journal of Paediatric Neurology, November 2017, Vol.21(6), pp.804-804 [Rivista Peer Reviewed]

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

Vill, Katharina ; Müller‐Felber, Wolfgang ; Alhaddad, Bader ; Strom, Tim M. ; Teusch, Veronika ; Weigand, Heike ; Blaschek, Astrid ; Meitinger, Thomas ; Haack, Tobias B.

Movement Disorders, May 2017, Vol.32(5), pp.797-799 [Rivista Peer Reviewed]

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Absence of an Orphan Mitochondrial Protein, C19orf12, Causes a Distinct Clinical Subtype of Neurodegeneration with Brain Iron Accumulation

Hartig, Monika b ; Iuso, Arcangela ; Haack, Tobias ; Kmiec, Tomasz ; Jurkiewicz, Elzbieta ; Heim, Katharina ; Roeber, Sigrun ; Tarabin, Victoria ; Dusi, Sabrina ; Krajewska-Walasek, Malgorzata ; Jozwiak, Sergiusz ; Hempel, Maja ; Winkelmann, Juliane ; Elstner, Matthias ; Oexle, Konrad ; Klopstock, Thomas ; Mueller-Felber, Wolfgang ; Gasser, Thomas ; Trenkwalder, Claudia

The American Journal of Human Genetics, 2011, Vol.89(4), pp.543-550 [Rivista Peer Reviewed]

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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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NAXE Mutations Disrupt the Cellular NAD(P)HX Repair System and Cause a Lethal Neurometabolic Disorder of Early Childhood

Kremer, Laura S ; Danhauser, Katharina ; Herebian, Diran ; Petkovic Ramadža, Danijela ; Piekutowska-Abramczuk, Dorota ; Seibt, Annette ; Müller-Felber, Wolfgang ; Haack, Tobias B ; Płoski, Rafał ; Lohmeier, Klaus ; Schneider, Dominik ; Klee, Dirk ; Rokicki, Dariusz ; Mayatepek, Ertan ; Strom, Tim M ; Meitinger, Thomas

The American Journal of Human Genetics, 06 October 2016, Vol.99(4), pp.894-902 [Rivista Peer Reviewed]

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Prevalence of Pompe disease in 3,076 patients with hyperCKemia and limb-girdle muscular weakness

Lukacs, A., Zoltan ; Nieves Cobos, C., Paulina ; Wenninger, C., Stephan ; Willis, C., Tracey ; Guglieri, C., Michela ; Roberts, C., Marc ; Quinlivan, C., Rosaline ; Hilton-Jones, C., David ; Evangelista, C., Teresinha ; Zierz, C., Stephan ; Schlotter-Weigel, C., Beate ; Walter, C., Maggie ; Reilich, C., Peter ; Klopstock, C., Thomas ; Deschauer, C., Marcus ; Straub, C., Volker ; Müller-Felber, C., Wolfgang ; Schoser, C., Benedikt

Neurology, 2016, Vol.87(3), pp.295-298 [Rivista Peer Reviewed]

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

Vill, Katharina ; Ille, Lena ; Schroeder, Sebastian A ; Blaschek, Astrid ; Müller-Felber, Wolfgang

European Journal of Paediatric Neurology, November 2015, Vol.19(6), pp.640-646 [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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da questo autore/creatore:

  1. Müller-Felber, Wolfgang
  2. Müller-Felber, W.
  3. Muller-Felber, W
  4. Vill, Katharina
  5. Mueller-Felber, Wolfgang

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