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.
Published in Clinical genetics (01.01.2016)
Published in Clinical genetics (01.01.2016)
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Journal Article
Enzyme replacement therapy with alglucosidase alfa in 44 patients with late-onset glycogen storage disease type 2: 12-month results of an observational clinical trial
Strothotte, S., Strigl-Pill, N., Grunert, B., Kornblum, C., Eger, K., Wessig, C., Deschauer, M., Breunig, F., Glocker, F. X., Vielhaber, S., Brejova, A., Hilz, M., Reiners, K., Müller-Felber, W., Mengel, E., Spranger, M., Schoser, Benedikt
Published in Journal of neurology (2010)
Published in Journal of neurology (2010)
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Journal Article
Consequences of mutations within the C terminus of the FHL1 gene
Schoser, B, Goebel, H H, Janisch, I, Quasthoff, S, Rother, J, Bergmann, M, Müller-Felber, W, Windpassinger, C
Published in Neurology (18.08.2009)
Published in Neurology (18.08.2009)
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Journal Article
Diagnosis and treatment of Guillain-Barré Syndrome in childhood and adolescence: An evidence- and consensus-based guideline
Korinthenberg, R., Trollmann, R., Felderhoff-Müser, U., Bernert, G., Hackenberg, A., Hufnagel, M., Pohl, M., Hahn, G., Mentzel, H.J., Sommer, C., Lambeck, J., Mecher, F., Hessenauer, M., Winterholler, C., Kempf, U., Jacobs, B.C., Rostasy, K., Müller-Felber, W.
Published in European journal of paediatric neurology (01.03.2020)
Published in European journal of paediatric neurology (01.03.2020)
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Journal Article
Novel SBF2 mutations and clinical spectrum of Charcot‐Marie‐Tooth neuropathy type 4B2
Laššuthová, P., Vill, K., Erdem‐Ozdamar, S., Schröder, J.M., Topaloglu, H., Horvath, R., Müller‐Felber, W., Bansagi, B., Schlotter‐Weigel, B., Gläser, D., Neupauerová, J., Sedláčková, L., Staněk, D., Mazanec, R., Weis, J., Seeman, P., Senderek, J.
Published in Clinical genetics (01.11.2018)
Published in Clinical genetics (01.11.2018)
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Journal Article
Qualitative and quantitative muscle ultrasound in patients with Duchenne muscular dystrophy: Where do sonographic changes begin?
Vill, K., Sehri, M., Müller, C., Hannibal, I., Huf, V., Idriess, M., Gerstl, L., Bonfert, M.V., Tacke, M., Schroeder, A.S., Landgraf, M.N., Müller-Felber, W., Blaschek, A.
Published in European journal of paediatric neurology (01.09.2020)
Published in European journal of paediatric neurology (01.09.2020)
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Journal Article
A recurrent single-amino acid deletion (p.Glu500del) in the head domain of ß-cardiac myosin in two unrelated boys presenting with polyhydramnios, congenital axial stiffness and skeletal myopathy
Bader, Ingrid, Freilinger, M, Landauer, F, Waldmüller, S, Mueller-Felber, W, Rauscher, C, Sperl, W, Bittner, R. E, Schmidt, W. M, Mayr, J. A
Published in Orphanet journal of rare diseases (19.07.2022)
Published in Orphanet journal of rare diseases (19.07.2022)
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Journal Article
Methods for a prompt and reliable laboratory diagnosis of Pompe disease: Report from an international consensus meeting
Winchester, B., Bali, D., Bodamer, O.A., Caillaud, C., Christensen, E., Cooper, A., Cupler, E., Deschauer, M., Fumić, K., Jackson, M., Kishnani, P., Lacerda, L., Ledvinová, J., Lugowska, A., Lukacs, Z., Maire, I., Mandel, H., Mengel, E., Müller-Felber, W., Piraud, M., Reuser, A., Rupar, T., Sinigerska, I., Szlago, M., Verheijen, F., van Diggelen, O.P., Wuyts, B., Zakharova, E., Keutzer, J.
Published in Molecular genetics and metabolism (01.03.2008)
Published in Molecular genetics and metabolism (01.03.2008)
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Journal Article
Conference Proceeding
Early white matter changes in childhood multiple sclerosis: a diffusion tensor imaging study
Blaschek, A, Keeser, D, Müller, S, Koerte, I K, Sebastian Schröder, A, Müller-Felber, W, Heinen, F, Ertl-Wagner, B
Published in American journal of neuroradiology : AJNR (01.10.2013)
Published in American journal of neuroradiology : AJNR (01.10.2013)
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Journal Article
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, G.M, Korinthenberg, R
Published in Neuromuscular disorders : NMD (01.02.2014)
Published in Neuromuscular disorders : NMD (01.02.2014)
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Journal Article
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
Published in Neuromuscular disorders : NMD (01.04.2016)
Published in Neuromuscular disorders : NMD (01.04.2016)
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Journal Article
Adjunctive lithium treatment in the prevention of suicidal behaviour in depressive disorders: a randomised, placebo-controlled, 1-year trial
Lauterbach, E., Felber, W., Müller-Oerlinghausen, B., Ahrens, B., Bronisch, T., Meyer, T., Kilb, B., Lewitzka, U., Hawellek, B., Quante, A., Richter, K., Broocks, A., Hohagen, F.
Published in Acta Psychiatrica Scandinavica (01.12.2008)
Published in Acta Psychiatrica Scandinavica (01.12.2008)
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Journal Article
Creatine monohydrate in muscular dystrophies: A double-blind, placebo-controlled clinical study
Walter, M C, Lochmüller, H, Reilich, P, Klopstock, T, Huber, R, Hartard, M, Hennig, M, Pongratz, D, Müller-Felber, W
Published in Neurology (09.05.2000)
Published in Neurology (09.05.2000)
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Journal Article
Impaired receptor clustering in congenital myasthenic syndrome with novel RAPSN mutations
Müller, J S, Baumeister, S K, Rasic, V M, Krause, S, Todorovic, S, Kugler, K, Müller-Felber, W, Abicht, A, Lochmüller, H
Published in Neurology (10.10.2006)
Published in Neurology (10.10.2006)
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Journal Article
Rapsyn N88K is a frequent cause of congenital myasthenic syndromes in European patients
Müller, J S, Mildner, G, Müller-Felber, W, Schara, U, Krampfl, K, Petersen, B, Petrova, S, Stucka, R, Mortier, W, Bufler, J, Kurlemann, G, Huebner, A, Merlini, L, Lochmüller, H, Abicht, A
Published in Neurology (10.06.2003)
Published in Neurology (10.06.2003)
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Journal Article
Spinal muscular atrophy : Time for newborn screening?
Vill, K, Blaschek, A, Schara, U, Kölbel, H, Hohenfellner, K, Harms, E, Olgemöller, B, Walter, Maggie C, Müller-Felber, W
Published in Nervenarzt (01.12.2017)
Published in Nervenarzt (01.12.2017)
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