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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2000 2
2001 1
2002 2
2004 4
2005 1
2006 2
2007 4
2008 3
2009 2
2010 3
2011 3
2012 2
2013 3
2014 1
2015 1
2016 2
2017 3
2018 1
2019 3
2020 2
2021 5
2022 4
2023 6
2024 4

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59 results

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Page 1
[Seronegative myasthenic syndrome?].
Selge C, Kümpfel T, Havla J, Schöberl F, Danek A, Reilich P. Selge C, et al. Among authors: reilich p. Nervenarzt. 2020 Feb;91(2):150-152. doi: 10.1007/s00115-019-00810-1. Nervenarzt. 2020. PMID: 31535177 German. 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.
Clinical and genetic features of amyotrophic lateral sclerosis patients with C9orf72 mutations.
Wiesenfarth M, Günther K, Müller K, Witzel S, Weiland U, Mayer K, Herrmann C, Brenner D, Schuster J, Freischmidt A, Lulé D, Meyer T, Regensburger M, Grehl T, Emmer A, Petri S, Großkreutz J, Rödiger A, Steinbach R, Klopstock T, Reilich P, Schöberl F, Wolf J, Hagenacker T, Weyen U, Zeller D, Ludolph AC, Dorst J. Wiesenfarth M, et al. Among authors: reilich p. Brain Commun. 2023 Mar 21;5(2):fcad087. doi: 10.1093/braincomms/fcad087. eCollection 2023. Brain Commun. 2023. PMID: 37006326 Free PMC article.
Spectrum and frequency of genetic variants in sporadic amyotrophic lateral sclerosis.
Ruf WP, Boros M, Freischmidt A, Brenner D, Grozdanov V, de Meirelles J, Meyer T, Grehl T, Petri S, Grosskreutz J, Weyen U, Guenther R, Regensburger M, Hagenacker T, Koch JC, Emmer A, Roediger A, Steinbach R, Wolf J, Weishaupt JH, Lingor P, Deschauer M, Cordts I, Klopstock T, Reilich P, Schoeberl F, Schrank B, Zeller D, Hermann A, Knehr A, Günther K, Dorst J, Schuster J, Siebert R, Ludolph AC, Müller K. Ruf WP, et al. Among authors: reilich p. Brain Commun. 2023 May 9;5(3):fcad152. doi: 10.1093/braincomms/fcad152. eCollection 2023. Brain Commun. 2023. PMID: 37223130 Free PMC article.
Cutaneous T-cell lymphoma mimicking myopathy with lipoatrophy.
Hiebeler M, Reinholz M, Flaig M, Schmidt C, Schoser B, Herzinger T, Abicht A, Reilich P. Hiebeler M, et al. Among authors: reilich p. Neuromuscul Disord. 2022 Jan;32(1):65-70. doi: 10.1016/j.nmd.2021.11.009. Epub 2021 Nov 20. Neuromuscul Disord. 2022. PMID: 34937683
Myelitis as a side effect of tofersen therapy in SOD1-associated ALS.
Reilich P, Schöberl F, Hiebeler M, Tonon M, Ludolph AC, Senel M. Reilich P, et al. J Neurol. 2024 Apr;271(4):2114-2118. doi: 10.1007/s00415-023-12130-1. Epub 2023 Dec 9. J Neurol. 2024. PMID: 38066205 Free PMC article. No abstract available.
Methylation of the 4q35 D4Z4 repeat defines disease status in facioscapulohumeral muscular dystrophy.
Erdmann H, Scharf F, Gehling S, Benet-Pagès A, Jakubiczka S, Becker K, Seipelt M, Kleefeld F, Knop KC, Prott EC, Hiebeler M, Montagnese F, Gläser D, Vorgerd M, Hagenacker T, Walter MC, Reilich P, Neuhann T, Zenker M, Holinski-Feder E, Schoser B, Abicht A. Erdmann H, et al. Among authors: reilich p. Brain. 2023 Apr 19;146(4):1388-1402. doi: 10.1093/brain/awac336. Brain. 2023. PMID: 36100962
Clinical Effectiveness of Newborn Screening for Spinal Muscular Atrophy: A Nonrandomized Controlled Trial.
Schwartz O, Vill K, Pfaffenlehner M, Behrens M, Weiß C, Johannsen J, Friese J, Hahn A, Ziegler A, Illsinger S, Smitka M, von Moers A, Kölbel H, Schreiber G, Kaiser N, Wilichowski E, Flotats-Bastardas M, Husain RA, Baumann M, Köhler C, Trollmann R, Schwerin-Nagel A, Eisenkölbl A, Schimmel M, Fleger M, Kauffmann B, Wiegand G, Baumgartner M, Rauscher C, Cirak S, Gläser D, Bernert G, Hagenacker T, Goldbach S, Probst-Schendzielorz K, Lochmüller H, Müller-Felber W, Schara-Schmidt U, Walter MC, Kirschner J, Pechmann A; SMARTCARE study group. Schwartz O, et al. JAMA Pediatr. 2024 Apr 8:e240492. doi: 10.1001/jamapediatrics.2024.0492. Online ahead of print. JAMA Pediatr. 2024. PMID: 38587854
59 results