Verhelst H - Search Results

1

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. 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.

2

A family with X-linked dominant Charcot-Marie-Tooth caused by a connexin32 mutation.

Verhelst HE, Lofgren A, Van Coster RN. Verhelst HE, et al. Eur J Paediatr Neurol. 2000;4(5):235-8. doi: 10.1053/ejpn.2000.0311. Eur J Paediatr Neurol. 2000. PMID: 11030070

3

A new mitochondrial point mutation in the transfer RNA(Leu) gene in a patient with a clinical phenotype resembling Kearns-Sayre syndrome.

Seneca S, Verhelst H, De Meirleir L, Meire F, Ceuterick-De Groote C, Lissens W, Van Coster R. Seneca S, et al. Among authors: verhelst h. Arch Neurol. 2001 Jul;58(7):1113-8. doi: 10.1001/archneur.58.7.1113. Arch Neurol. 2001. PMID: 11448301 Review.

4

Blue native polyacrylamide gel electrophoresis: a powerful tool in diagnosis of oxidative phosphorylation defects.

Van Coster R, Smet J, George E, De Meirleir L, Seneca S, Van Hove J, Sebire G, Verhelst H, De Bleecker J, Van Vlem B, Verloo P, Leroy J. Van Coster R, et al. Among authors: verhelst h. Pediatr Res. 2001 Nov;50(5):658-65. doi: 10.1203/00006450-200111000-00020. Pediatr Res. 2001. PMID: 11641463

5

Retrospective study of topiramate in a paediatric population with intractable epilepsy showing promising effects in the West syndrome patients.

Thijs J, Verhelst H, Van Coster R. Thijs J, et al. Among authors: verhelst h. Acta Neurol Belg. 2001 Sep;101(3):171-6. Acta Neurol Belg. 2001. PMID: 11817266 Clinical Trial.

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: verhelst h. 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. J Child Neurol. 2005 Nov;20(11):911-3. doi: 10.1177/08830738050200110901. J Child Neurol. 2005. PMID: 16417862

8

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. Neurology. 2007 Jul 10;69(2):218-9. doi: 10.1212/01.wnl.0000265597.56202.6c. Neurology. 2007. PMID: 17620557 No abstract available.

9

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. 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

10

Vagus nerve stimulation for refractory status epilepticus.

De Herdt V, Waterschoot L, Vonck K, Dermaut B, Verhelst H, Van Coster R, De Jaeger A, Van Roost D, Boon P. De Herdt V, et al. Among authors: verhelst h. Eur J Paediatr Neurol. 2009 May;13(3):286-9. doi: 10.1016/j.ejpn.2008.05.004. Epub 2008 Jun 27. Eur J Paediatr Neurol. 2009. PMID: 18585939

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