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

Year Number of Results
1986 1
1987 2
1988 3
1989 3
1990 6
1991 5
1992 10
1993 4
1994 3
1995 8
1996 4
1997 11
1998 7
1999 8
2000 2
2001 1
2002 7
2003 8
2004 4
2005 9
2006 5
2007 5
2008 9
2009 8
2010 4
2011 6
2012 6
2013 8
2014 7
2015 6
2016 6
2017 9
2018 5
2019 13
2020 3
2021 2
2022 2
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Publication date

Search Results

196 results
Results by year
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Page 1
GRIN2A-related disorders: genotype and functional consequence predict phenotype.
Strehlow V, Heyne HO, Vlaskamp DRM, Marwick KFM, Rudolf G, de Bellescize J, Biskup S, Brilstra EH, Brouwer OF, Callenbach PMC, Hentschel J, Hirsch E, Kind PC, Mignot C, Platzer K, Rump P, Skehel PA, Wyllie DJA, Hardingham GE, van Ravenswaaij-Arts CMA, Lesca G, Lemke JR; GRIN2A study group. Strehlow V, et al. Among authors: brouwer of. Brain. 2019 Jan 1;142(1):80-92. doi: 10.1093/brain/awy304. Brain. 2019. PMID: 30544257 Free PMC article.
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: brouwer of. 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.
Acute flaccid myelitis and enterovirus D68: lessons from the past and present.
Helfferich J, Knoester M, Van Leer-Buter CC, Neuteboom RF, Meiners LC, Niesters HG, Brouwer OF. Helfferich J, et al. Among authors: brouwer of. Eur J Pediatr. 2019 Sep;178(9):1305-1315. doi: 10.1007/s00431-019-03435-3. Epub 2019 Jul 23. Eur J Pediatr. 2019. PMID: 31338675 Free PMC article. Review.
Cohesin complex-associated holoprosencephaly.
Kruszka P, Berger SI, Casa V, Dekker MR, Gaesser J, Weiss K, Martinez AF, Murdock DR, Louie RJ, Prijoles EJ, Lichty AW, Brouwer OF, Zonneveld-Huijssoon E, Stephan MJ, Hogue J, Hu P, Tanima-Nagai M, Everson JL, Prasad C, Cereda A, Iascone M, Schreiber A, Zurcher V, Corsten-Janssen N, Escobar L, Clegg NJ, Delgado MR, Hajirnis O, Balasubramanian M, Kayserili H, Deardorff M, Poot RA, Wendt KS, Lipinski RJ, Muenke M. Kruszka P, et al. Among authors: brouwer of. Brain. 2019 Sep 1;142(9):2631-2643. doi: 10.1093/brain/awz210. Brain. 2019. PMID: 31334757 Free PMC article.
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: brouwer of. 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.
[Epileptic seizures in children].
Brouwer OF. Brouwer OF. Ned Tijdschr Geneeskd. 1999 Jan 23;143(4):190-3. Ned Tijdschr Geneeskd. 1999. PMID: 10086140 Review. Dutch.
Migraine and epilepsy: genetically linked?
Haan J, van den Maagdenberg AM, Brouwer OF, Ferrari MD. Haan J, et al. Among authors: brouwer of. Expert Rev Neurother. 2008 Sep;8(9):1307-11. doi: 10.1586/14737175.8.9.1307. Expert Rev Neurother. 2008. PMID: 18759542 Review.
The outcome of childhood epilepsy: what improvements are needed?
Camfield P, Camfield C, Arts WF, Brouwer OF, Arzimanoglou A. Camfield P, et al. Among authors: brouwer of. Epileptic Disord. 2013 Jun;15(2):101-4. doi: 10.1684/epd.2013.0583. Epileptic Disord. 2013. PMID: 23774399 Free article. No abstract available.
196 results