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

Year Number of Results
1990 1
1991 1
1998 1
1999 1
2000 1
2001 2
2004 2
2005 2
2006 2
2007 1
2009 1
2010 2
2011 3
2012 4
2013 3
2014 1
2015 2
2016 5
2017 1
2018 3
2019 1
2020 1
2023 0
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35 results
Results by year
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Page 1
Increased axonal ribosome numbers in CMT diseases.
Verheijen MH, Lammens M, Ceuterick-de Groote C, Timmerman V, De Jonghe P, King RH, Smit AB, van Minnen J. Verheijen MH, et al. Among authors: ceuterick de groote c. J Peripher Nerv Syst. 2011 Mar;16(1):71-3. doi: 10.1111/j.1529-8027.2011.00322.x. J Peripher Nerv Syst. 2011. PMID: 21504506 No abstract available.
Neuropathology in classical and variant ataxia-telangiectasia.
Verhagen MM, Martin JJ, van Deuren M, Ceuterick-de Groote C, Weemaes CM, Kremer BH, Taylor MA, Willemsen MA, Lammens M. Verhagen MM, et al. Among authors: ceuterick de groote c. Neuropathology. 2012 Jun;32(3):234-44. doi: 10.1111/j.1440-1789.2011.01263.x. Epub 2011 Oct 24. Neuropathology. 2012. PMID: 22017321
Cathepsin A-related arteriopathy with strokes and leukoencephalopathy (CARASAL).
Bugiani M, Kevelam SH, Bakels HS, Waisfisz Q, Ceuterick-de Groote C, Niessen HW, Abbink TE, Lesnik Oberstein SA, van der Knaap MS. Bugiani M, et al. Among authors: ceuterick de groote c. Neurology. 2016 Oct 25;87(17):1777-1786. doi: 10.1212/WNL.0000000000003251. Epub 2016 Sep 24. Neurology. 2016. PMID: 27664989
Mutated CTSF in adult-onset neuronal ceroid lipofuscinosis and FTD.
van der Zee J, Mariën P, Crols R, Van Mossevelde S, Dillen L, Perrone F, Engelborghs S, Verhoeven J, D'aes T, Ceuterick-De Groote C, Sieben A, Versijpt J, Cras P, Martin JJ, Van Broeckhoven C. van der Zee J, et al. Among authors: ceuterick de groote c. Neurol Genet. 2016 Sep 16;2(5):e102. doi: 10.1212/NXG.0000000000000102. eCollection 2016 Oct. Neurol Genet. 2016. PMID: 27668283 Free PMC article.
Teenage-onset progressive myoclonic epilepsy due to a familial C9orf72 repeat expansion.
van den Ameele J, Jedlickova I, Pristoupilova A, Sieben A, Van Mossevelde S, Ceuterick-de Groote C, Hůlková H, Matej R, Meurs A, Van Broeckhoven C, Berkovic SF, Santens P, Kmoch S, Dermaut B. van den Ameele J, et al. Among authors: ceuterick de groote c. Neurology. 2018 Feb 20;90(8):e658-e663. doi: 10.1212/WNL.0000000000004999. Epub 2018 Jan 19. Neurology. 2018. PMID: 29352102
Distal myopathy with upper limb predominance caused by filamin C haploinsufficiency.
Guergueltcheva V, Peeters K, Baets J, Ceuterick-de Groote C, Martin JJ, Suls A, De Vriendt E, Mihaylova V, Chamova T, Almeida-Souza L, Ydens E, Tzekov C, Hadjidekov G, Gospodinova M, Storm K, Reyniers E, Bichev S, van der Ven PF, Fürst DO, Mitev V, Lochmüller H, Timmerman V, Tournev I, De Jonghe P, Jordanova A. Guergueltcheva V, et al. Among authors: ceuterick de groote c. Neurology. 2011 Dec 13;77(24):2105-14. doi: 10.1212/WNL.0b013e31823dc51e. Epub 2011 Nov 30. Neurology. 2011. PMID: 22131542
Functional characterization of novel MFSD8 pathogenic variants anticipates neurological involvement in juvenile isolated maculopathy.
Bauwens M, Storch S, Weisschuh N, Ceuterick-de Groote C, De Rycke R, Guillemyn B, De Jaegere S, Coppieters F, Van Coster R, Leroy BP, De Baere E. Bauwens M, et al. Among authors: ceuterick de groote c. Clin Genet. 2020 Mar;97(3):426-436. doi: 10.1111/cge.13673. Epub 2019 Dec 12. Clin Genet. 2020. PMID: 31721179 Free PMC article.
35 results