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Male patients affected by mosaic PCDH19 mutations: five new cases.
de Lange IM, Rump P, Neuteboom RF, Augustijn PB, Hodges K, Kistemaker AI, Brouwer OF, Mancini GMS, Newman HA, Vos YJ, Helbig KL, Peeters-Scholte C, Kriek M, Knoers NV, Lindhout D, Koeleman BPC, van Kempen MJA, Brilstra EH. de Lange IM, et al. Among authors: brouwer of. Neurogenetics. 2017 Jul;18(3):147-153. doi: 10.1007/s10048-017-0517-5. Epub 2017 Jul 1. Neurogenetics. 2017. PMID: 28669061 Free PMC article.
Hereditary epilepsy syndromes.
Callenbach PM, Brouwer OF. Callenbach PM, et al. Among authors: brouwer of. Clin Neurol Neurosurg. 1997 Aug;99(3):159-71. doi: 10.1016/s0303-8467(97)00019-x. Clin Neurol Neurosurg. 1997. PMID: 9350396 Review.
Angelman syndrome: a review of clinical and genetic aspects.
Laan LA, v Haeringen A, Brouwer OF. Laan LA, et al. Among authors: brouwer of. Clin Neurol Neurosurg. 1999 Sep;101(3):161-70. doi: 10.1016/s0303-8467(99)00030-x. Clin Neurol Neurosurg. 1999. PMID: 10536901 Review.
X-linked hydrocephalus.
Willems PJ, Brouwer OF, Dijkstra I, Wilmink J. Willems PJ, et al. Among authors: brouwer of. Am J Med Genet. 1987 Aug;27(4):921-8. doi: 10.1002/ajmg.1320270419. Am J Med Genet. 1987. PMID: 3425602
PRRT2 mutation causes benign familial infantile convulsions.
de Vries B, Callenbach PM, Kamphorst JT, Weller CM, Koelewijn SC, ten Houten R, de Coo IF, Brouwer OF, van den Maagdenberg AM. de Vries B, et al. Among authors: brouwer of. Neurology. 2012 Nov 20;79(21):2154-5. doi: 10.1212/WNL.0b013e3182752c30. Epub 2012 Oct 17. Neurology. 2012. PMID: 23077019
Refinement of the chromosome 16 locus for benign familial infantile convulsions.
Callenbach PM, van den Boogerd EH, de Coo RF, ten Houten R, Oosterwijk JC, Hageman G, Frants RR, Brouwer OF, van den Maagdenberg AM. Callenbach PM, et al. Among authors: brouwer of. Clin Genet. 2005 Jun;67(6):517-25. doi: 10.1111/j.1399-0004.2005.00445.x. Clin Genet. 2005. PMID: 15857419
204 results