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

Year Number of Results
1986 1
1988 3
1989 2
1991 1
1992 1
1993 1
1994 1
1995 1
1998 1
2001 1
2002 1
2009 1
2011 6
2012 3
2013 2
2014 4
2015 3
2016 2
2017 5
2018 9
2019 5
2020 6
2021 10
2022 5
2023 4
2024 1

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66 results

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Page 1
The electrophysiological footprint of CACNA1A disorders.
Indelicato E, Unterberger I, Nachbauer W, Eigentler A, Amprosi M, Zeiner F, Haberlandt E, Kaml M, Gizewski E, Boesch S. Indelicato E, et al. Among authors: eigentler a. J Neurol. 2021 Jul;268(7):2493-2505. doi: 10.1007/s00415-021-10415-x. Epub 2021 Feb 5. J Neurol. 2021. PMID: 33544220 Free PMC article. Review.
Skeletal muscle transcriptomics dissects the pathogenesis of Friedreich's ataxia.
Indelicato E, Kirchmair A, Amprosi M, Steixner S, Nachbauer W, Eigentler A, Wahl N, Apostolova G, Krogsdam A, Schneider R, Wanschitz J, Trajanoski Z, Boesch S. Indelicato E, et al. Among authors: eigentler a. Hum Mol Genet. 2023 Jun 19;32(13):2241-2250. doi: 10.1093/hmg/ddad051. Hum Mol Genet. 2023. PMID: 37027192 Free PMC article.
Familial writer's cramp: a clinical clue for inherited coenzyme Q10 deficiency.
Amprosi M, Zech M, Steiger R, Nachbauer W, Eigentler A, Gizewski ER, Guger M, Indelicato E, Boesch S. Amprosi M, et al. Among authors: eigentler a. Neurogenetics. 2021 Mar;22(1):81-86. doi: 10.1007/s10048-020-00624-3. Epub 2020 Aug 24. Neurogenetics. 2021. PMID: 32830305 Free PMC article.
SYNE1-ataxia: Novel genotypic and phenotypic findings.
Indelicato E, Nachbauer W, Fauth C, Krabichler B, Schossig A, Eigentler A, Dichtl W, Wenning G, Wagner M, Fanciulli A, Janecke A, Boesch S. Indelicato E, et al. Among authors: eigentler a. Parkinsonism Relat Disord. 2019 May;62:210-214. doi: 10.1016/j.parkreldis.2018.12.007. Epub 2018 Dec 11. Parkinsonism Relat Disord. 2019. PMID: 30573412
Clinical management guidelines for Friedreich ataxia: best practice in rare diseases.
Corben LA, Collins V, Milne S, Farmer J, Musheno A, Lynch D, Subramony S, Pandolfo M, Schulz JB, Lin K, Delatycki MB; Clinical Management Guidelines Writing Group. Corben LA, et al. Orphanet J Rare Dis. 2022 Nov 12;17(1):415. doi: 10.1186/s13023-022-02568-3. Orphanet J Rare Dis. 2022. PMID: 36371255 Free PMC article.
Autonomic function testing in Friedreich's ataxia.
Indelicato E, Fanciulli A, Ndayisaba JP, Nachbauer W, Eigentler A, Granata R, Wanschitz J, Poewe W, Wenning GK, Boesch S. Indelicato E, et al. Among authors: eigentler a. J Neurol. 2018 Sep;265(9):2015-2022. doi: 10.1007/s00415-018-8946-0. Epub 2018 Jun 27. J Neurol. 2018. PMID: 29951702 Free PMC article.
Instrumented gait analysis defines the walking signature of CACNA1A disorders.
Indelicato E, Raccagni C, Runer S, Hannink J, Nachbauer W, Eigentler A, Amprosi M, Wenning G, Boesch S. Indelicato E, et al. Among authors: eigentler a. J Neurol. 2022 Jun;269(6):2941-2947. doi: 10.1007/s00415-021-10878-y. Epub 2021 Nov 9. J Neurol. 2022. PMID: 34755206 Free PMC article.
Targeting the glucocorticoid receptor signature gene Mono Amine Oxidase-A enhances the efficacy of chemo- and anti-androgen therapy in advanced prostate cancer.
Puhr M, Eigentler A, Handle F, Hackl H, Ploner C, Heidegger I, Schaefer G, Brandt MP, Hoefer J, Van der Pluijm G, Klocker H. Puhr M, et al. Among authors: eigentler a. Oncogene. 2021 Apr;40(17):3087-3100. doi: 10.1038/s41388-021-01754-0. Epub 2021 Apr 1. Oncogene. 2021. PMID: 33795839 Free PMC article.
66 results