Meiners LC - Search Results

1

Dyskinesia Impairment Scale scores in Dutch pre-school children after neonatal therapeutic hypothermia.

Kuiper MJ, Meiners LC, Chandler ES, Brandsma R, Bos AF, Horst HT, Sival DA; Neonatal neurologic Assessment Group. Kuiper MJ, et al. Among authors: meiners lc. Eur J Paediatr Neurol. 2020 Sep;28:70-76. doi: 10.1016/j.ejpn.2020.07.013. Epub 2020 Aug 5. Eur J Paediatr Neurol. 2020. PMID: 32950367 Free article.

2

The influence of cerebral malformations on the quality of general movements in spina bifida aperta.

Sival DA, Brouwer OF, Meiners LC, Sauer PJ, Prechtl HF, Bos AF. Sival DA, et al. Among authors: meiners lc. Eur J Pediatr Surg. 2003 Dec;13 Suppl 1:S29-30. Eur J Pediatr Surg. 2003. PMID: 14986607 No abstract available.

3

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: meiners lc. 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

4

Diffusion tensor imaging and magnetic resonance spectroscopy of the brain in a patient with Sturge-Weber syndrome.

Sijens PE, Gieteling EW, Meiners LC, Sival DA, Potze JH, Irwan R, Oudkerk M. Sijens PE, et al. Among authors: meiners lc. Acta Radiol. 2006 Nov;47(9):972-6. doi: 10.1080/02841850600849100. Acta Radiol. 2006. PMID: 17077050

5

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: meiners lc. Cerebrospinal Fluid Res. 2008 Mar 1;5:4. doi: 10.1186/1743-8454-5-4. Cerebrospinal Fluid Res. 2008. PMID: 18312688 Free PMC article.

6

1H magnetic resonance spectroscopy in monocarboxylate transporter 8 gene deficiency.

Sijens PE, Rödiger LA, Meiners LC, Lunsing RJ. Sijens PE, et al. Among authors: meiners lc. J Clin Endocrinol Metab. 2008 May;93(5):1854-9. doi: 10.1210/jc.2007-2441. Epub 2008 Mar 4. J Clin Endocrinol Metab. 2008. PMID: 18319316

7

Quantitative multivoxel 1H MR spectroscopy of the brain in children with acute liver failure.

Sijens PE, Alkefaji H, Lunsing RJ, van Spronsen FJ, Meiners LC, Oudkerk M, Verkade HJ. Sijens PE, et al. Among authors: meiners lc. Eur Radiol. 2008 Nov;18(11):2601-9. doi: 10.1007/s00330-008-1049-z. Epub 2008 May 21. Eur Radiol. 2008. PMID: 18493780

8

Magnetic resonance imaging and proton magnetic resonance spectroscopy of the brain in the diagnostic evaluation of developmental delay.

Verbruggen KT, Meiners LC, Sijens PE, Lunsing RJ, van Spronsen FJ, Brouwer OF. Verbruggen KT, et al. Among authors: meiners lc. Eur J Paediatr Neurol. 2009 Mar;13(2):181-90. doi: 10.1016/j.ejpn.2008.04.014. Epub 2008 Jun 24. Eur J Paediatr Neurol. 2009. PMID: 18579422

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: meiners lc. J Magn Reson Imaging. 2009 Oct;30(4):716-21. doi: 10.1002/jmri.21909. J Magn Reson Imaging. 2009. PMID: 19787717

10

Bilateral polymicrogyria as the indicative feature in a child with a 22q11.2 deletion.

Gerkes EH, Hordijk R, Dijkhuizen T, Sival DA, Meiners LC, Sikkema-Raddatz B, van Ravenswaaij-Arts CM. Gerkes EH, et al. Among authors: meiners lc. Eur J Med Genet. 2010 Sep-Oct;53(5):344-6. doi: 10.1016/j.ejmg.2010.05.003. Epub 2010 May 27. Eur J Med Genet. 2010. PMID: 20553986

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