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Sensory neuropathy due to RFC1 in a patient with ALS: more than a coincidence?
Schoeberl F, Abicht A, Kuepper C, Voelk S, Sonnenfeld S, Tonon M, Schaub A, Scholz V, Kleinle S, Erdmann H, Wolf DA, Reilich P. Schoeberl F, et al. Among authors: reilich p. J Neurol. 2022 May;269(5):2774-2777. doi: 10.1007/s00415-021-10835-9. Epub 2021 Nov 25. J Neurol. 2022. PMID: 34821988 Free PMC article. No abstract available.
[Molecular therapies in muscular dystrophies].
Walter MC, Reilich P. Walter MC, et al. Among authors: reilich p. Fortschr Neurol Psychiatr. 2018 Sep;86(9):535-542. doi: 10.1055/a-0624-9513. Epub 2018 Sep 24. Fortschr Neurol Psychiatr. 2018. PMID: 30248686 Review. German.
The phenotypic spectrum of neutral lipid storage myopathy due to mutations in the PNPLA2 gene.
Reilich P, Horvath R, Krause S, Schramm N, Turnbull DM, Trenell M, Hollingsworth KG, Gorman GS, Hans VH, Reimann J, MacMillan A, Turner L, Schollen A, Witte G, Czermin B, Holinski-Feder E, Walter MC, Schoser B, Lochmüller H. Reilich P, et al. J Neurol. 2011 Nov;258(11):1987-97. doi: 10.1007/s00415-011-6055-4. Epub 2011 May 5. J Neurol. 2011. PMID: 21544567
Prevalence of Pompe disease in 3,076 patients with hyperCKemia and limb-girdle muscular weakness.
Lukacs Z, Nieves Cobos P, Wenninger S, Willis TA, Guglieri M, Roberts M, Quinlivan R, Hilton-Jones D, Evangelista T, Zierz S, Schlotter-Weigel B, Walter MC, Reilich P, Klopstock T, Deschauer M, Straub V, Müller-Felber W, Schoser B. Lukacs Z, et al. Among authors: reilich p. Neurology. 2016 Jul 19;87(3):295-8. doi: 10.1212/WNL.0000000000002758. Epub 2016 May 11. Neurology. 2016. PMID: 27170567 Free PMC article.
Rare diagnosis of telethoninopathy (LGMD2G) in a Turkish patient.
Ikenberg E, Karin I, Ertl-Wagner B, Abicht A, Bulst S, Krause S, Schoser B, Reilich P, Walter MC. Ikenberg E, et al. Among authors: reilich p. Neuromuscul Disord. 2017 Sep;27(9):856-860. doi: 10.1016/j.nmd.2017.05.017. Epub 2017 Jun 1. Neuromuscul Disord. 2017. PMID: 28666572
59 results