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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 2
2022 2
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42 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.
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.
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.
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.
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.
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.
Regional Brain and Spinal Cord Volume Loss in Spinocerebellar Ataxia Type 3.
Faber J, Schaprian T, Berkan K, Reetz K, França MC Jr, de Rezende TJR, Hong J, Liao W, van de Warrenburg B, van Gaalen J, Durr A, Mochel F, Giunti P, Garcia-Moreno H, Schoels L, Hengel H, Synofzik M, Bender B, Oz G, Joers J, de Vries JJ, Kang JS, Timmann-Braun D, Jacobi H, Infante J, Joules R, Romanzetti S, Diedrichsen J, Schmid M, Wolz R, Klockgether T. Faber J, et al. Among authors: van gaalen j. Mov Disord. 2021 Oct;36(10):2273-2281. doi: 10.1002/mds.28610. Epub 2021 May 5. Mov Disord. 2021. PMID: 33951232
Polyglutamine-Expanded Ataxin-3: A Target Engagement Marker for Spinocerebellar Ataxia Type 3 in Peripheral Blood.
Hübener-Schmid J, Kuhlbrodt K, Peladan J, Faber J, Santana MM, Hengel H, Jacobi H, Reetz K, Garcia-Moreno H, Raposo M, van Gaalen J, Infante J, Steiner KM, de Vries J, Verbeek MM, Giunti P, Pereira de Almeida L, Lima M, van de Warrenburg B, Schöls L, Klockgether T, Synofzik M; European Spinocerebellar Ataxia Type-3/Machado-Joseph Disease Initiative (ESMI) Study Group, Riess O. Hübener-Schmid J, et al. Among authors: van gaalen j. Mov Disord. 2021 Nov;36(11):2675-2681. doi: 10.1002/mds.28749. Epub 2021 Aug 16. Mov Disord. 2021. PMID: 34397117
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.
42 results