Van Coster R - Search Results

1

Hypocretin-1 deficiency in a girl with ROHHAD syndrome.

Dhondt K, Verloo P, Verhelst H, Van Coster R, Overeem S. Dhondt K, et al. Among authors: van coster r. Pediatrics. 2013 Sep;132(3):e788-92. doi: 10.1542/peds.2012-3225. Epub 2013 Aug 12. Pediatrics. 2013. PMID: 23940246

2

Lambert-Eaton myasthenic syndrome in a 13-year-old girl with Xp11.22-p11.23 duplication.

Verbeek S, Vanakker O, Mercelis R, Lipka AF, Haerynck F, Dullaers M, Verloo P, Van Coster R, Verhelst H. Verbeek S, et al. Among authors: van coster r. Eur J Paediatr Neurol. 2014 May;18(3):439-43. doi: 10.1016/j.ejpn.2014.01.001. Epub 2014 Jan 15. Eur J Paediatr Neurol. 2014. PMID: 24461257

3

Childhood narcolepsy with partial facial cataplexy: a diagnostic dilemma.

Dhondt K, Verhelst H, Pevernagie D, Slap F, Van Coster R. Dhondt K, et al. Among authors: van coster r. Sleep Med. 2009 Aug;10(7):797-8. doi: 10.1016/j.sleep.2008.08.005. Epub 2009 Jan 14. Sleep Med. 2009. PMID: 19147400

4

Anti-NMDA-receptor encephalitis in a 3 year old patient with chromosome 6p21.32 microdeletion including the HLA cluster.

Verhelst H, Verloo P, Dhondt K, De Paepe B, Menten B, Dalmau J, Van Coster R. Verhelst H, et al. Among authors: van coster r. Eur J Paediatr Neurol. 2011 Mar;15(2):163-6. doi: 10.1016/j.ejpn.2010.07.004. Epub 2010 Aug 6. Eur J Paediatr Neurol. 2011. PMID: 20692195 Free PMC article.

5

Palatal insufficiency as isolated sign of GQ1b antibody syndrome.

Verhelst H, Maes M, Deblaere K, Van Coster R. Verhelst H, et al. Among authors: van coster r. Pediatr Neurol. 2011 Apr;44(4):292-4. doi: 10.1016/j.pediatrneurol.2010.11.010. Pediatr Neurol. 2011. PMID: 21397172

6

Hot-water epilepsy: a new Caucasian case.

De Keyzer K, Corthouts I, Van Coster R, Verhelst H. De Keyzer K, et al. Among authors: van coster r. Eur J Pediatr. 2005 Mar;164(3):184-5. doi: 10.1007/s00431-004-1595-6. Epub 2004 Dec 1. Eur J Pediatr. 2005. PMID: 15578219 No abstract available.

7

Neuroradiologic findings in a young patient with characteristics of Sturge-Weber syndrome and Klippel-Trenaunay syndrome.

Verhelst H, Van Coster R. Verhelst H, et al. Among authors: van coster r. J Child Neurol. 2005 Nov;20(11):911-3. doi: 10.1177/08830738050200110901. J Child Neurol. 2005. PMID: 16417862

8

Perisylvian polymicrogyria, infantile spasms and arthrogryposis: the severe end of the spectrum of congenital bilateral perisylvian polymicrogyria.

De Coene A, Van Coster R, Verhelst H. De Coene A, et al. Among authors: van coster r. Eur J Paediatr Neurol. 2010 May;14(3):270-3. doi: 10.1016/j.ejpn.2009.05.005. Epub 2009 Jun 25. Eur J Paediatr Neurol. 2010. PMID: 19559633

9

Limbic encephalitis as presentation of a SAP deficiency.

Verhelst H, Van Coster R, Bockaert N, Laureys G, Latour S, Fischer A, Haerynck F. Verhelst H, et al. Among authors: van coster r. Neurology. 2007 Jul 10;69(2):218-9. doi: 10.1212/01.wnl.0000265597.56202.6c. Neurology. 2007. PMID: 17620557 No abstract available.

10

Hippocampal atrophy and developmental regression as first sign of linear scleroderma "en coup de sabre".

Verhelst HE, Beele H, Joos R, Vanneuville B, Van Coster RN. Verhelst HE, et al. Among authors: van coster rn. Eur J Paediatr Neurol. 2008 Nov;12(6):508-11. doi: 10.1016/j.ejpn.2007.12.001. Epub 2008 Jan 22. Eur J Paediatr Neurol. 2008. PMID: 18207439

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