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

Year Number of Results
1984 1
1989 3
1990 2
1991 1
1992 5
1993 4
1995 1
1996 3
1997 1
1999 3
2000 2
2001 3
2002 4
2003 6
2004 8
2005 2
2006 3
2007 5
2008 3
2009 3
2010 3
2011 1
2012 4
2013 4
2014 5
2015 6
2016 4
2017 4
2018 3
2019 3
2020 4
2021 1
2022 1
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96 results
Results by year
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Page 1
A novel diagnostic approach to patients with myoclonus.
Zutt R, van Egmond ME, Elting JW, van Laar PJ, Brouwer OF, Sival DA, Kremer HP, de Koning TJ, Tijssen MA. Zutt R, et al. Among authors: kremer hp. Nat Rev Neurol. 2015 Dec;11(12):687-97. doi: 10.1038/nrneurol.2015.198. Epub 2015 Nov 10. Nat Rev Neurol. 2015. PMID: 26553594 Review.
Reviewing the genetic causes of spastic-ataxias.
de Bot ST, Willemsen MA, Vermeer S, Kremer HP, van de Warrenburg BP. de Bot ST, et al. Among authors: kremer hp. Neurology. 2012 Oct 2;79(14):1507-14. doi: 10.1212/WNL.0b013e31826d5fb0. Neurology. 2012. PMID: 23033504 Review.
A clinical diagnostic algorithm for early onset cerebellar ataxia.
Brandsma R, Verschuuren-Bemelmans CC, Amrom D, Barisic N, Baxter P, Bertini E, Blumkin L, Brankovic-Sreckovic V, Brouwer OF, Bürk K, Catsman-Berrevoets CE, Craiu D, de Coo IFM, Gburek J, Kennedy C, de Koning TJ, Kremer HPH, Kumar R, Macaya A, Micalizzi A, Mirabelli-Badenier M, Nemeth A, Nuovo S, Poll-The B, Lerman-Sagie T, Steinlin M, Synofzik M, Tijssen MAJ, Vasco G, Willemsen MAAP, Zanni G, Valente EM, Boltshauser E, Sival DA. Brandsma R, et al. Among authors: kremer hph. Eur J Paediatr Neurol. 2019 Sep;23(5):692-706. doi: 10.1016/j.ejpn.2019.08.004. Epub 2019 Aug 10. Eur J Paediatr Neurol. 2019. PMID: 31481303 Review.
What's wrong with Tourette syndrome?
Kremer HP. Kremer HP. Parkinsonism Relat Disord. 2007;13 Suppl 3:S385-6. doi: 10.1016/S1353-8020(08)70034-8. Parkinsonism Relat Disord. 2007. PMID: 18267268 Review.
The cerebral metabolic topography of spinocerebellar ataxia type 3.
Meles SK, Kok JG, De Jong BM, Renken RJ, de Vries JJ, Spikman JM, Ziengs AL, Willemsen ATM, van der Horn HJ, Leenders KL, Kremer HPH. Meles SK, et al. Among authors: kremer hph. Neuroimage Clin. 2018 Mar 29;19:90-97. doi: 10.1016/j.nicl.2018.03.038. eCollection 2018. Neuroimage Clin. 2018. PMID: 30035006 Free PMC article.
Child neurology: hereditary spastic paraplegia in children.
de Bot ST, van de Warrenburg BP, Kremer HP, Willemsen MA. de Bot ST, et al. Among authors: kremer hp. Neurology. 2010 Nov 9;75(19):e75-9. doi: 10.1212/WNL.0b013e3181fc2776. Neurology. 2010. PMID: 21060088 Review. No abstract available.
Adult metachromatic leukodystrophy treated by allo-SCT and a review of the literature.
de Hosson LD, van de Warrenburg BP, Preijers FW, Blijlevens NM, van der Reijden BA, Kremer HP, Lefeber DJ, Allebes WA, Al-Ali H, Niederwieser DW, Schaap NP, Schattenberg AV. de Hosson LD, et al. Among authors: kremer hp. Bone Marrow Transplant. 2011 Aug;46(8):1071-6. doi: 10.1038/bmt.2010.252. Epub 2010 Nov 1. Bone Marrow Transplant. 2011. PMID: 21042305 Review.
Riluzole in patients with hereditary cerebellar ataxia.
Brandsma R, Kremer HPH, Sival DA. Brandsma R, et al. Among authors: kremer hph. Lancet Neurol. 2016 Jul;15(8):788. doi: 10.1016/S1474-4422(16)00131-9. Lancet Neurol. 2016. PMID: 27302351 No abstract available.
96 results