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

Year Number of Results
1993 1
1997 1
1998 1
1999 3
2000 3
2001 1
2002 3
2003 3
2004 5
2005 4
2006 5
2007 2
2008 1
2009 6
2010 7
2011 6
2012 11
2013 7
2014 7
2015 8
2016 9
2017 9
2018 7
2019 9
2020 15
2021 10
2022 8
2023 1
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123 results
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Page 1
Congenital Myasthenic Syndromes Overview.
Abicht A, Müller JS, Lochmüller H. Abicht A, et al. 2003 May 9 [updated 2021 Dec 23]. In: Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2023. 2003 May 9 [updated 2021 Dec 23]. In: Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2023. PMID: 20301347 Free Books & Documents. Review.
Persistent hypokalaemia and intermittent muscle weakness.
Rabenstein M, Abicht A, Brunn A, Lehmann H, Wunderlich G. Rabenstein M, et al. Among authors: abicht a. Pract Neurol. 2022 Dec;22(6):518-520. doi: 10.1136/pn-2022-003433. Epub 2022 Jul 30. Pract Neurol. 2022. PMID: 35907633
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: abicht a. 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
The Curse of Apneic Spells.
Radke J, Dreesmann M, Radke M, von Moers A, Abicht A, Stenzel W, Goebel HH. Radke J, et al. Among authors: abicht a. Semin Pediatr Neurol. 2018 Jul;26:56-58. doi: 10.1016/j.spen.2017.03.006. Epub 2017 Apr 13. Semin Pediatr Neurol. 2018. PMID: 29961520
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: abicht a. Brain. 2022 Sep 14:awac336. doi: 10.1093/brain/awac336. Online ahead of print. Brain. 2022. PMID: 36100962
Novel TPM3 mutation in a family with cap myopathy and review of the literature.
Schreckenbach T, Schröder JM, Voit T, Abicht A, Neuen-Jacob E, Roos A, Bulst S, Kuhl C, Schulz JB, Weis J, Claeys KG. Schreckenbach T, et al. Among authors: abicht a. Neuromuscul Disord. 2014 Feb;24(2):117-24. doi: 10.1016/j.nmd.2013.10.002. Epub 2013 Oct 23. Neuromuscul Disord. 2014. PMID: 24239060 Review.
A Novel Gain-of-Function Nav1.9 Mutation in a Child With Episodic Pain.
Huang J, Estacion M, Zhao P, Dib-Hajj FB, Schulman B, Abicht A, Kurth I, Brockmann K, Waxman SG, Dib-Hajj SD. Huang J, et al. Among authors: abicht a. Front Neurosci. 2019 Sep 3;13:918. doi: 10.3389/fnins.2019.00918. eCollection 2019. Front Neurosci. 2019. PMID: 31551682 Free PMC article.
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: abicht a. 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.
A new case of limb girdle muscular dystrophy 2G in a Greek patient, founder effect and review of the literature.
Brusa R, Magri F, Papadimitriou D, Govoni A, Del Bo R, Ciscato P, Savarese M, Cinnante C, Walter MC, Abicht A, Bulst S, Corti S, Moggio M, Bresolin N, Nigro V, Comi GP. Brusa R, et al. Among authors: abicht a. Neuromuscul Disord. 2018 Jun;28(6):532-537. doi: 10.1016/j.nmd.2018.04.006. Epub 2018 Apr 13. Neuromuscul Disord. 2018. PMID: 29759638 Review.
123 results