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Year Number of Results
1993 1
2008 1
2009 1
2011 2
2012 3
2013 2
2014 1
2015 1
2016 3
2017 1
2018 2
2019 6
2020 4
2021 4
2022 4
2023 7
2024 2

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35 results

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Page 1
GNAO1-Related Disorder.
Briere L, Thiel M, Sweetser DA, Koy A, Axeen E. Briere L, et al. Among authors: koy a. 2023 Nov 9. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2023 Nov 9. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 37956232 Free Books & Documents. Review.
Long-Term Follow-Up of Pediatric Patients with Dyskinetic Cerebral Palsy and Deep Brain Stimulation.
Koy A, Kühn AA, Schiller P, Huebl J, Schneider GH, Eckenweiler M, Rensing-Zimmermann C, Coenen VA, Krauss JK, Saryyeva A, Hartmann H, Lorenz D, Volkmann J, Matthies C, Schnitzler A, Vesper J, Gharabaghi A, Weiss D, Bevot A, Marks W, Howser A, Monbaliu E, Mueller J, Prinz-Langenohl R, Visser-Vandewalle V, Timmermann L; STIM-CP investigators. Koy A, et al. Mov Disord. 2023 Sep;38(9):1736-1742. doi: 10.1002/mds.29516. Epub 2023 Jun 26. Mov Disord. 2023. PMID: 37358761
Advances in management of movement disorders in children.
Koy A, Lin JP, Sanger TD, Marks WA, Mink JW, Timmermann L. Koy A, et al. Lancet Neurol. 2016 Jun;15(7):719-735. doi: 10.1016/S1474-4422(16)00132-0. Epub 2016 May 9. Lancet Neurol. 2016. PMID: 27302239 Review.
Genotype-phenotype correlation and treatment effects in young patients with GNAO1-associated disorders.
Thiel M, Bamborschke D, Janzarik WG, Assmann B, Zittel S, Patzer S, Auhuber A, Opp J, Matzker E, Bevot A, Seeger J, van Baalen A, Stüve B, Brockmann K, Cirak S, Koy A. Thiel M, et al. Among authors: koy a. J Neurol Neurosurg Psychiatry. 2023 Oct;94(10):806-815. doi: 10.1136/jnnp-2022-330261. Epub 2023 May 24. J Neurol Neurosurg Psychiatry. 2023. PMID: 37225406
PNPT1 mutations may cause Aicardi-Goutières-Syndrome.
Bamborschke D, Kreutzer M, Koy A, Koerber F, Lucas N, Huenseler C, Herkenrath P, Lee-Kirsch MA, Cirak S. Bamborschke D, et al. Among authors: koy a. Brain Dev. 2021 Feb;43(2):320-324. doi: 10.1016/j.braindev.2020.10.005. Epub 2020 Nov 4. Brain Dev. 2021. PMID: 33158637
The genomic and clinical landscape of fetal akinesia.
Pergande M, Motameny S, Özdemir Ö, Kreutzer M, Wang H, Daimagüler HS, Becker K, Karakaya M, Ehrhardt H, Elcioglu N, Ostojic S, Chao CM, Kawalia A, Duman Ö, Koy A, Hahn A, Reimann J, Schoner K, Schänzer A, Westhoff JH, Schwaibold EMC, Cossee M, Imbert-Bouteille M, von Pein H, Haliloglu G, Topaloglu H, Altmüller J, Nürnberg P, Thiele H, Heller R, Cirak S. Pergande M, et al. Among authors: koy a. Genet Med. 2020 Mar;22(3):511-523. doi: 10.1038/s41436-019-0680-1. Epub 2019 Nov 4. Genet Med. 2020. PMID: 31680123 Free article.
The phenotypic spectrum of PCDH12 associated disorders - Five new cases and review of the literature.
Fazeli W, Bamborschke D, Moawia A, Bakhtiari S, Tafakhori A, Giersdorf M, Hahn A, Weik A, Kolzter K, Shafiee S, Jin SC, Körber F, Lee-Kirsch MA, Darvish H, Cirak S, Kruer MC, Koy A. Fazeli W, et al. Among authors: koy a. Eur J Paediatr Neurol. 2022 Jan;36:7-13. doi: 10.1016/j.ejpn.2021.10.011. Epub 2021 Oct 30. Eur J Paediatr Neurol. 2022. PMID: 34773825 Free PMC article. Review.
Diffusion tensor imaging in pediatric patients with dystonia.
Loução R, Burkhardt J, Wirths J, Kabbasch C, Dembek TA, Heiden P, Cirak S, Al-Fatly B, Treuer H, Visser-Vandewalle V, Hoevels M, Koy A. Loução R, et al. Among authors: koy a. Neuroimage. 2024 Feb 15;287:120507. doi: 10.1016/j.neuroimage.2024.120507. Epub 2024 Jan 18. Neuroimage. 2024. PMID: 38244876 Free article.
35 results