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

Year Number of Results
1966 1
1967 1
1971 1
1988 3
2001 1
2011 3
2012 6
2013 3
2014 4
2015 2
2016 1
2017 1
2018 4
2019 9
2020 6
2021 1
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39 results
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Page 1
KIF1A variants are a frequent cause of autosomal dominant hereditary spastic paraplegia.
Pennings M, Schouten MI, van Gaalen J, Meijer RPP, de Bot ST, Kriek M, Saris CGJ, van den Berg LH, van Es MA, Zuidgeest DMH, Elting MW, van de Kamp JM, van Spaendonck-Zwarts KY, Die-Smulders C, Brilstra EH, Verschuuren CC, de Vries BBA, Bruijn J, Sofou K, Duijkers FA, Jaeger B, Schieving JH, van de Warrenburg BP, Kamsteeg EJ. Pennings M, et al. Among authors: van gaalen j. Eur J Hum Genet. 2020 Jan;28(1):40-49. doi: 10.1038/s41431-019-0497-z. Epub 2019 Sep 5. Eur J Hum Genet. 2020. PMID: 31488895 Free PMC article.
Sjögren-Larsson syndrome: The mild end of the phenotypic spectrum.
Staps P, van Gaalen J, van Domburg P, Steijlen PM, Ferdinandusse S, den Heijer T, Seyger MMB, Theelen T, Willemsen MAAP. Staps P, et al. Among authors: van gaalen j. JIMD Rep. 2020 Mar 25;53(1):61-70. doi: 10.1002/jmd2.12099. eCollection 2020 May. JIMD Rep. 2020. PMID: 32395410 Free PMC article.
The preclinical stage of spinocerebellar ataxias.
Maas RP, van Gaalen J, Klockgether T, van de Warrenburg BP. Maas RP, et al. Among authors: van gaalen j. Neurology. 2015 Jul 7;85(1):96-103. doi: 10.1212/WNL.0000000000001711. Epub 2015 Jun 10. Neurology. 2015. PMID: 26062625 Review.
Movement disorders in spinocerebellar ataxias.
van Gaalen J, Giunti P, van de Warrenburg BP. van Gaalen J, et al. Mov Disord. 2011 Apr;26(5):792-800. doi: 10.1002/mds.23584. Epub 2011 Mar 2. Mov Disord. 2011. PMID: 21370272 Review.
Drug-induced cerebellar ataxia: a systematic review.
van Gaalen J, Kerstens FG, Maas RP, Härmark L, van de Warrenburg BP. van Gaalen J, et al. CNS Drugs. 2014 Dec;28(12):1139-53. doi: 10.1007/s40263-014-0200-4. CNS Drugs. 2014. PMID: 25391707 Review.
Inclusion body myositis in patients with spinocerebellar ataxia types 3 and 6.
Rietveld A, van Gaalen J, Saris C, Okkersen K, Küsters B, van de Warrenburg B, van Engelen B, Sacconi S, Raaphorst J. Rietveld A, et al. Among authors: van gaalen j. J Neurol Neurosurg Psychiatry. 2020 Aug;91(8):876-878. doi: 10.1136/jnnp-2020-323270. Epub 2020 Jun 23. J Neurol Neurosurg Psychiatry. 2020. PMID: 32576615
Classic ataxia-telangiectasia: the phenotype of long-term survivors.
van Os NJH, van Deuren M, Weemaes CMR, van Gaalen J, Hijdra H, Taylor AMR, van de Warrenburg BPC, Willemsen MAAP. van Os NJH, et al. Among authors: van gaalen j. J Neurol. 2020 Mar;267(3):830-837. doi: 10.1007/s00415-019-09641-1. Epub 2019 Nov 27. J Neurol. 2020. PMID: 31776720 Free PMC article.
A hereditary spastic paraplegia predominant phenotype caused by variants in the NEFL gene.
Mul K, Schouten MI, van der Looij E, Dooijes D, Hennekam FAM, Notermans NC, Praamstra P, van Gaalen J, Kamsteeg EJ, Verbeek NE, van de Warrenburg BPC. Mul K, et al. Among authors: van gaalen j. Parkinsonism Relat Disord. 2020 Nov;80:98-101. doi: 10.1016/j.parkreldis.2020.09.016. Epub 2020 Sep 12. Parkinsonism Relat Disord. 2020. PMID: 32979786 Free article.
De novo SPAST mutations may cause a complex SPG4 phenotype.
Schieving JH, de Bot ST, van de Pol LA, Wolf NI, Brilstra EH, Frints SG, van Gaalen J, Misra-Isrie M, Pennings M, Verschuuren-Bemelmans CC, Kamsteeg EJ, van de Warrenburg BP, Willemsen MA. Schieving JH, et al. Among authors: van gaalen j. Brain. 2019 Jul 1;142(7):e31. doi: 10.1093/brain/awz140. Brain. 2019. PMID: 31157359 No abstract available.
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