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

Year Number of Results
1993 2
1996 1
1997 3
1998 3
1999 2
2000 10
2001 5
2002 3
2003 5
2004 4
2005 3
2006 4
2007 1
2008 5
2009 4
2010 5
2011 4
2012 5
2013 3
2014 5
2015 7
2016 3
2017 8
2018 10
2019 8
2020 5
2021 5
2022 4
2023 3
2024 1
2025 1

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114 results

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Page 1
Autosomal recessive limb-girdle and Miyoshi muscular dystrophies in the Netherlands: The clinical and molecular spectrum of 244 patients.
Ten Dam L, Frankhuizen WS, Linssen WHJP, Straathof CS, Niks EH, Faber K, Fock A, Kuks JB, Brusse E, de Coo R, Voermans N, Verrips A, Hoogendijk JE, van der Pol L, Westra D, de Visser M, van der Kooi AJ, Ginjaar I. Ten Dam L, et al. Among authors: verrips a. Clin Genet. 2019 Aug;96(2):126-133. doi: 10.1111/cge.13544. Epub 2019 May 6. Clin Genet. 2019. PMID: 30919934
[Cerebrotendinous xanthomatosis].
Verrips A. Verrips A. Ned Tijdschr Geneeskd. 2001 Sep 1;145(35):1673-7. Ned Tijdschr Geneeskd. 2001. PMID: 11561482 Dutch.
[Awakening ptosis].
Nobels-Janssen E, de Kort FAS, Linn FHH, Verrips A. Nobels-Janssen E, et al. Among authors: verrips a. Ned Tijdschr Geneeskd. 2021 Dec 20;165:D6108. Ned Tijdschr Geneeskd. 2021. PMID: 35138710 Dutch.
Movement disorders in cerebrotendinous xanthomatosis.
Stelten BML, van de Warrenburg BPC, Wevers RA, Verrips A. Stelten BML, et al. Among authors: verrips a. Parkinsonism Relat Disord. 2019 Jan;58:12-16. doi: 10.1016/j.parkreldis.2018.07.006. Epub 2018 Jul 19. Parkinsonism Relat Disord. 2019. PMID: 30054180 Review.
Cerebrotendinous xanthomatosis without neurological involvement.
Stelten BML, Raal FJ, Marais AD, Riksen NP, Roeters van Lennep JE, Duell PB, van der Graaf M, Kluijtmans LAJ, Wevers RA, Verrips A. Stelten BML, et al. Among authors: verrips a. J Intern Med. 2021 Nov;290(5):1039-1047. doi: 10.1111/joim.13277. Epub 2021 Apr 8. J Intern Med. 2021. PMID: 33830582 Free article.
Hepatitis E: A breathtaking virus.
van de Wardt J, Verrips A, van Griensven CHS, van Eijk JJJ. van de Wardt J, et al. Among authors: verrips a. Neurol Clin Pract. 2019 Oct;9(5):e39-e41. doi: 10.1212/CPJ.0000000000000600. Neurol Clin Pract. 2019. PMID: 31750032 Free PMC article. No abstract available.
Hypoglycorrhachia: a simple clue, simply missed.
Willemsen MA, Verrips A, Verbeek MM, Voit T, Klepper J. Willemsen MA, et al. Among authors: verrips a. Ann Neurol. 2001 May;49(5):685-6. Ann Neurol. 2001. PMID: 11357965 No abstract available.
A novel seven-octapeptide repeat insertion in the prion protein gene (PRNP) in a Dutch pedigree with Gerstmann-Sträussler-Scheinker disease phenotype: comparison with similar cases from the literature.
Jansen C, Voet W, Head MW, Parchi P, Yull H, Verrips A, Wesseling P, Meulstee J, Baas F, van Gool WA, Ironside JW, Rozemuller AJ. Jansen C, et al. Among authors: verrips a. Acta Neuropathol. 2011 Jan;121(1):59-68. doi: 10.1007/s00401-010-0656-3. Epub 2010 Mar 3. Acta Neuropathol. 2011. PMID: 20198483 Free PMC article. Review.
114 results