E-LIB Suche - Ergebnisse für: Verhelst, H.

1

Paediatric acute disseminated encephalomyelitis followed by..:

Wong, Y. Y. M. ; Hacohen, Y. ; Armangue, T....
European Journal of Neurology. 25 (2018) 5 - p. 782-786 , 2018

Link: https://doi.org/10.1111/..

2

PP13.9 – 2836: Variants in the NR3C2 gene as possible genet..:

Verhelst, H. ; Mets, G. ; Verloo, P....
European Journal of Paediatric Neurology. 19 (2015) - p. S84 , 2015

Link: https://doi.org/10.1016/..

3

PP08.8 – 2833: Multiple sclerosis in Belgian children: A mu..:

Verhelst, H. ; De Waele, L. ; Deconinck, N....
European Journal of Paediatric Neurology. 19 (2015) - p. S62 , 2015

Link: https://doi.org/10.1016/..

4

PP15.3 – 2545: Everolimus for patients with subependymal gi..:

Fogarasi, A. ; De Waele, L. ; Bartalini, G....
European Journal of Paediatric Neurology. 19 (2015) - p. S90 , 2015

Link: https://doi.org/10.1016/..

5

P123 – 1742 Extensive multifocal demyelinating encephalomye..:

Verhelst, H ; Maes, M ; Meersschaut, V..
European Journal of Paediatric Neurology. 17 (2013) - p. S87 , 2013

Link: https://doi.org/10.1016/..

6

P304 – 1516 Lambert-Eaton myasthenic syndrome in a 13-year-..:

Verbeek, S ; Vanakker, O ; Mercelis, R...
European Journal of Paediatric Neurology. 17 (2013) - p. S137 , 2013

Link: https://doi.org/10.1016/..

7

Clinical and genetic aspects of PCDH19-related epilepsy syn..:

van Harssel, J. J. T. ; Weckhuysen, S. ; van Kempen, M. J. A....
neurogenetics. 14 (2013) 1 - p. 23-34 , 2013

Link: https://doi.org/10.1007/..

8

Colon transit time and anorectal manometry in children and ..:

Velde, S. Vande ; Pratte, L. ; Verhelst, H....
International Journal of Colorectal Disease. 28 (2013) 11 - p. 1547-1553 , 2013

Link: https://doi.org/10.1007/..

9

P314 – 1862 Clinical and behavioral characteristics of chil..:

Dhondt, K ; Verloo, P ; Verhelst, H.
European Journal of Paediatric Neurology. 17 (2013) - p. S140 , 2013

Link: https://doi.org/10.1016/..

10

Temps du transit colique chez l'enfant atteint de dysraphis..:

Pratte, L. ; Vande Velde, S. ; Meersschaut, V....
Archives de Pédiatrie. 20 (2013) 8 - p. 831-836 , 2013

Link: https://doi.org/10.1016/..

11

Polymicrogyria with dysmorphic basal ganglia? Think tubulin:

Amrom, D. ; Tanyalçin, I. ; Verhelst, H....
Clinical Genetics. 85 (2013) 2 - p. 178-183 , 2013

Link: https://doi.org/10.1111/..

12

TUBA1Amutations: From isolated lissencephaly to familial po..:

Jansen, A.C. ; Oostra, A. ; Desprechins, B....
Neurology. 76 (2011) 11 - p. 988-992 , 2011

Link: https://doi.org/10.1212/..

13

1FC4.4 Neurological presentation in children with familial ..:

Verhelst, H. ; Verloo, P. ; Mondelaers, V....
European Journal of Paediatric Neurology. 15 (2011) - p. S17 , 2011

Link: https://doi.org/10.1016/..

14

P07.18 Cerebral Capillary Telangiectasias:

Verbeek, S. ; Verloo, P. ; Verhelst, H....
European Journal of Paediatric Neurology. 15 (2011) - p. S64 , 2011

Link: https://doi.org/10.1016/..

15

P19.6 Multiple sclerosis in a 12 year old boy with an inher..:

Verhelst, H. ; Verloo, P. ; Menten, B..
European Journal of Paediatric Neurology. 15 (2011) - p. S109 , 2011

Link: https://doi.org/10.1016/..