Brouwer OF - Search Results

1

Visual screening of muscle ultrasound images in children.

Brandsma R, Verbeek RJ, Maurits NM, van der Hoeven JH, Brouwer OF, den Dunnen WF, Burger H, Sival DA. Brandsma R, et al. Among authors: brouwer of. Ultrasound Med Biol. 2014 Oct;40(10):2345-51. doi: 10.1016/j.ultrasmedbio.2014.03.027. Epub 2014 Jul 9. Ultrasound Med Biol. 2014. PMID: 25023119

2

Neonatal loss of motor function in human spina bifida aperta.

Sival DA, van Weerden TW, Vles JS, Timmer A, den Dunnen WF, Staal-Schreinemachers AL, Hoving EW, Sollie KM, Kranen-Mastenbroek VJ, Sauer PJ, Brouwer OF. Sival DA, et al. Among authors: brouwer of. Pediatrics. 2004 Aug;114(2):427-34. doi: 10.1542/peds.114.2.427. Pediatrics. 2004. PMID: 15286226

3

Intermittent prednisone therapy in Duchenne muscular dystrophy: a randomized controlled trial.

Beenakker EA, Fock JM, Van Tol MJ, Maurits NM, Koopman HM, Brouwer OF, Van der Hoeven JH. Beenakker EA, et al. Among authors: brouwer of. Arch Neurol. 2005 Jan;62(1):128-32. doi: 10.1001/archneur.62.1.128. Arch Neurol. 2005. PMID: 15642859 Clinical Trial.

4

Functional ability and muscle force in healthy children and ambulant Duchenne muscular dystrophy patients.

Beenakker EA, Maurits NM, Fock JM, Brouwer OF, van der Hoeven JH. Beenakker EA, et al. Among authors: brouwer of. Eur J Paediatr Neurol. 2005;9(6):387-93. doi: 10.1016/j.ejpn.2005.06.004. Epub 2005 Aug 15. Eur J Paediatr Neurol. 2005. PMID: 16102988

5

Shah-Waardenburg syndrome and PCWH associated with SOX10 mutations: a case report and review of the literature.

Verheij JB, Sival DA, van der Hoeven JH, Vos YJ, Meiners LC, Brouwer OF, van Essen AJ. Verheij JB, et al. Among authors: brouwer of. Eur J Paediatr Neurol. 2006 Jan;10(1):11-7. doi: 10.1016/j.ejpn.2005.10.004. Epub 2006 Feb 28. Eur J Paediatr Neurol. 2006. PMID: 16504559

6

The amplitude of the Achilles tendon reflex in infants is related to body position.

Bruggink JL, Bos AF, vd Hoeven JH, Brouwer OF, Sollie KM, Sival DA. Bruggink JL, et al. Among authors: brouwer of. Early Hum Dev. 2006 Nov;82(11):715-20. doi: 10.1016/j.earlhumdev.2006.03.001. Epub 2006 May 2. Early Hum Dev. 2006. PMID: 16631326

7

Pathogenesis of cerebral malformations in human fetuses with meningomyelocele.

de Wit OA, den Dunnen WF, Sollie KM, Muñoz RI, Meiners LC, Brouwer OF, Rodríguez EM, Sival DA. de Wit OA, et al. Among authors: brouwer of. Cerebrospinal Fluid Res. 2008 Mar 1;5:4. doi: 10.1186/1743-8454-5-4. Cerebrospinal Fluid Res. 2008. PMID: 18312688 Free PMC article.

8

Novel homozygous ALS2 nonsense mutation (p.Gln715X) in sibs with infantile-onset ascending spastic paralysis: the first cases from northwestern Europe.

Verschuuren-Bemelmans CC, Winter P, Sival DA, Elting JW, Brouwer OF, Müller U. Verschuuren-Bemelmans CC, et al. Among authors: brouwer of. Eur J Hum Genet. 2008 Nov;16(11):1407-11. doi: 10.1038/ejhg.2008.108. Epub 2008 Jun 4. Eur J Hum Genet. 2008. PMID: 18523452

9

Quantitative multivoxel proton spectroscopy of the brain in developmental delay.

Verbruggen KT, Maurits NM, Meiners LC, Brouwer OF, van Spronsen FJ, Sijens PE. Verbruggen KT, et al. Among authors: brouwer of. J Magn Reson Imaging. 2009 Oct;30(4):716-21. doi: 10.1002/jmri.21909. J Magn Reson Imaging. 2009. PMID: 19787717

10

The EEG response to pyridoxine-IV neither identifies nor excludes pyridoxine-dependent epilepsy.

Bok LA, Maurits NM, Willemsen MA, Jakobs C, Teune LK, Poll-The BT, de Coo IF, Toet MC, Hagebeuk EE, Brouwer OF, van der Hoeven JH, Sival DA. Bok LA, et al. Among authors: brouwer of. Epilepsia. 2010 Dec;51(12):2406-11. doi: 10.1111/j.1528-1167.2010.02747.x. Epub 2010 Sep 30. Epilepsia. 2010. PMID: 20887371 Free article.

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