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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 12
2009 10
2010 4
2011 6
2012 6
2013 8
2014 8
2015 6
2016 6
2017 9
2018 5
2019 13
2020 4
2021 2
2022 3
2023 2
2024 0

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204 results

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Page 1
Clinical spectrum of 4H leukodystrophy caused by POLR3A and POLR3B mutations.
Wolf NI, Vanderver A, van Spaendonk RM, Schiffmann R, Brais B, Bugiani M, Sistermans E, Catsman-Berrevoets C, Kros JM, Pinto PS, Pohl D, Tirupathi S, Strømme P, de Grauw T, Fribourg S, Demos M, Pizzino A, Naidu S, Guerrero K, van der Knaap MS, Bernard G; 4H Research Group. Wolf NI, et al. Neurology. 2014 Nov 18;83(21):1898-905. doi: 10.1212/WNL.0000000000001002. Epub 2014 Oct 22. Neurology. 2014. PMID: 25339210 Free PMC article.
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.
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.
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.
Epidemiology of acute flaccid myelitis in children in the Netherlands, 2014 to 2019.
Helfferich J, de Lange MM, Benschop KS, Jacobs BC, Van Leer-Buter CC, Meijer A, Bakker DP, de Bie E, Braakman HM, Brandsma R, Neuteboom RF, Niks EH, Niermeijer JM, Roelfsema V, Schoenmaker N, Sie LT, Niesters HG, Brouwer OF, Te Wierik MJ. Helfferich J, et al. Among authors: brouwer of. Euro Surveill. 2022 Oct;27(42):2200157. doi: 10.2807/1560-7917.ES.2022.27.42.2200157. Euro Surveill. 2022. PMID: 36268734 Free PMC article. Review.
Unusual Course of Lafora Disease.
Zutt R, Drost G, Vos YJ, Elting JW, Miedema I, Tijssen MAJ, Brouwer OF, de Jong BM. Zutt R, et al. Among authors: brouwer of. Epilepsia Open. 2016 Aug 25;1(3-4):136-139. doi: 10.1002/epi4.12009. eCollection 2016 Dec. Epilepsia Open. 2016. PMID: 29588937 Free PMC article.
Pediatric acute flaccid myelitis: Evaluation of diagnostic criteria and differentiation from other causes of acute flaccid paralysis.
Helfferich J, Neuteboom RF, de Lange MMA, Benschop KSM, Van Leer-Buter CC, Meijer A, Bakker DP, de Bie E, Braakman HMH, Brandsma R, Niks EH, Niermeijer JM, Roelfsema V, Schoenmaker N, Sie LT, Niesters HG, Te Wierik MJM, Jacobs BC, Brouwer OF. Helfferich J, et al. Among authors: brouwer of. Eur J Paediatr Neurol. 2023 May;44:28-36. doi: 10.1016/j.ejpn.2023.03.002. Epub 2023 Mar 22. Eur J Paediatr Neurol. 2023. PMID: 36996587 Free article.
204 results