Scapuloperoneal syndrome type Kaeser and a wide phenotypic spectrum of adult-onset, dominant myopathies are associated with the desmin mutation R350P
Walter, M. C., Reilich, P., Huebner, A., Fischer, D., Schröder, R., Vorgerd, M., Kress, W., Born, C., Schoser, B. G., Krause, K. H., Klutzny, U., Bulst, S., Frey, J. R., Lochmüller, H.
Published in Brain (London, England : 1878) (01.06.2007)
Published in Brain (London, England : 1878) (01.06.2007)
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Journal Article
Alterations in the trapezius muscle in young patients with migraine – A pilot case series with MRI
Landgraf, M.N, Ertl-Wagner, B, Koerte, I.K, Thienel, J, Langhagen, T, Straube, A, von Kries, R, Reilich, P, Pomschar, A, Heinen, F
Published in European journal of paediatric neurology (01.05.2015)
Published in European journal of paediatric neurology (01.05.2015)
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Journal Article
P541: The impact of spinal muscular atrophies with regard to patients’ quality of life: a socio-economic analysis of a German patient cohort
Schreiber, O, Klug, C, Thiele, S, Herrmann, C, Zowe, J, Reilich, P, Nagels, K, Walter, M.C
Published in Clinical neurophysiology (01.06.2014)
Published in Clinical neurophysiology (01.06.2014)
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Journal Article
G.P.166
Schreiber, O, Klug, C, Thiele, S, Schorling, E, Zowe, J, Reilich, P, Nagels, K, Walter, M.C
Published in Neuromuscular disorders : NMD (01.10.2014)
Published in Neuromuscular disorders : NMD (01.10.2014)
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Journal Article
Evaluation of Cost Of Illness (COI) and health care burden in Spinal Muscular Atrophies (SMA)
Klug, C, Thiele, S, Herrmann, C, Zowe, J, Reilich, P, Nagels, K, Walter, M.C
Published in Journal of the neurological sciences (15.10.2013)
Published in Journal of the neurological sciences (15.10.2013)
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Journal Article
Long-term efficiency of intravenously administered immunoglobulin in anti-Yo syndrome with paraneoplastic cerebellar degeneration
Schessl, J., Schuberth, M., Reilich, P., Schneiderat, P., Strigl-Pill, N., Walter, M. C., Schlotter-Weigel, B., Schoser, B.
Published in Journal of neurology (01.05.2011)
Published in Journal of neurology (01.05.2011)
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Journal Article
Seronegative myasthenic syndrome?
Selge, C, Kümpfel, T, Havla, J, Schöberl, F, Danek, A, Reilich, P
Published in Nervenarzt (01.02.2020)
Published in Nervenarzt (01.02.2020)
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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
Ten-year follow-up in a case series of integrative botulinum toxin intervention in adolescents with chronic daily headache and associated muscle pain
Schroeder, A S, Huss, K, Blaschek, A, Koerte, I K, Zeycan, B, Roser, T, Langhagen, T, Schwerin, A, Berweck, S, Reilich, P, Schaefer, J, Straube, A, Heinen, F
Published in Neuropediatrics (01.12.2012)
Published in Neuropediatrics (01.12.2012)
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Journal Article
P75 Muscle MRI findings in LGMD2L
Sarkozy, A, Hicks, P, Miller, J, Walter, M.C, Reilich, P, Radunovic, A, Vaidya, S.S, Lochmüller, H, Bushby, K, Straub, V
Published in Neuromuscular disorders : NMD (2011)
Published in Neuromuscular disorders : NMD (2011)
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Journal Article
P4.27 Muscle MRI findings in anoctaminopathy
Sarkozy, A, Hicks, D, Miller, J, Walter, M.C, Reilich, P, Lochmuller, H, Bushby, K, Straub, V
Published in Neuromuscular disorders : NMD (01.10.2010)
Published in Neuromuscular disorders : NMD (01.10.2010)
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Journal Article
P64 Neutral lipid storage myopathy due to PNPLA2 mutations may respond to beta-adrenergic treatment
Horvath, R, Reilich, P, Krause, S, Turnbull, D.M, Trenell, M, Hollingsworth, K.G, Gorman, G.S, Czermin, B, Holinski-Feder, E, Walter, M.C, Schoser, B, Lochmüller, H
Published in Neuromuscular disorders : NMD (2011)
Published in Neuromuscular disorders : NMD (2011)
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Journal Article
Brain imaging and neuropsychology in late-onset dementia due to a novel mutation (R93C) of valosin-containing protein
Krause, S, Göhringer, T, Walter, M C, Schoser, B G H, Reilich, P, Linn, J, Pöpperl, G E, Frölich, L, Hentschel, F, Lochmüller, H, Danek, A
Published in Clinical neuropathology (01.09.2007)
Published in Clinical neuropathology (01.09.2007)
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Journal Article
FKRP (826C>A) frequently causes limb-girdle muscular dystrophy in German patients
Walter, M C, Petersen, J A, Stucka, R, Fischer, D, Schröder, R, Vorgerd, M, Schroers, A, Schreiber, H, Hanemann, C O, Knirsch, U, Rosenbohm, A, Huebner, A, Barisic, N, Horvath, R, Komoly, S, Reilich, P, Müller-Felber, W, Pongratz, D, Müller, J S, Auerswald, E A, Lochmüller, H
Published in Journal of medical genetics (01.04.2004)
Published in Journal of medical genetics (01.04.2004)
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Journal Article
De novo missense mutation in a constitutively expressed exon of the slow alpha-tropomyosin gene TPM3 associated with an atypical, sporadic case of nemaline myopathy
Durling, H.J, Reilich, P, Müller-Höcker, J, Mendel, B, Pongratz, D, Wallgren-Pettersson, C, Gunning, P, Lochmüller, H, Laing, N.G
Published in Neuromuscular disorders : NMD (01.12.2002)
Published in Neuromuscular disorders : NMD (01.12.2002)
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Journal Article
P.47 - Congenital centronuclear myopathy and epidermolysis bullosa due to two novel mutations in the plectin gene
Walter, M., Reilich, P., Krause, S., Abicht, A., Schoser, B.
Published in Neuromuscular disorders : NMD (01.10.2017)
Published in Neuromuscular disorders : NMD (01.10.2017)
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Journal Article
Congenital centronuclear myopathy and epidermolysis bullosa due to two novel mutations in the plectin gene
Walter, M., Reilich, P., Krause, S., Abicht, A., Schoser, B.
Published in Neuromuscular disorders : NMD (01.10.2017)
Published in Neuromuscular disorders : NMD (01.10.2017)
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Journal Article
LGMD 2I due to the common mutation 826C>A in the FKRP gene presenting as myopathy with vacuoles and paired-helical filaments
Reilich, P, Petersen, J A, Vielhaber, S, Mawrin, C, Schneider-Gold, C, Sommer, C, Reiners, K, Deschauer, M, Pongratz, D, Lochmüller, H, Walter, M C
Published in Acta myologica (01.10.2006)
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Published in Acta myologica (01.10.2006)
Journal Article
Respiratory insufficiency as a presenting symptom of LGMD2D in adulthood
Walter, M C, Dekomien, G, Schlotter-Weigel, B, Reilich, P, Pongratz, D, Müller-Felber, W, Epplen, J T, Huebner, A, Lochmüller, H
Published in Acta myologica (01.05.2004)
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Published in Acta myologica (01.05.2004)
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