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Acta Neurologica Belgica|May 22, 2026
Breaking the seizure cycle: Belgian expert consensus on the diagnostics and treatment of acute convulsive seizures in childrenA Aeby, B Ceulemans, K Jansen, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 16, 2013
[Colon transit time in children and young adults with open spinal dysraphism]L Pratte, S Vande Velde, V Meersschaut, et al.Acta Neurologica Belgica|August 2, 2003
Anti-epileptogenesis research: the clinical relevanceL Lagae, G Buyse, B Ceulemans, et al.Chemistry & Biology|February 27, 2013
A substrate-inspired probe monitors translocation, activation, and subcellular targeting of bacterial type III effector protease AvrPphBHaibin Lu, Zheming Wang, Mohammed Shabab, et al.Neurology|March 16, 2011
TUBA1A mutations: from isolated lissencephaly to familial polymicrogyriaA C Jansen, A Oostra, B Desprechins, et al.Pediatric Research|October 20, 2001
Blue native polyacrylamide gel electrophoresis: a powerful tool in diagnosis of oxidative phosphorylation defectsR Van Coster, J Smet, E George, et al.Clinical Genetics|March 19, 2013
Polymicrogyria with dysmorphic basal ganglia? Think tubulin!D Amrom, I Tanyalçin, H Verhelst, et al.European Journal of Neurology|February 15, 2018
Paediatric acute disseminated encephalomyelitis followed by optic neuritis: disease course, treatment response and outcomeY Y M Wong, Y Hacohen, T Armangue, et al.Neurogenetics|January 22, 2013
Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disordersJ J T van Harssel, S Weckhuysen, M J A van Kempen, et al.European Journal of Medical Genetics|March 25, 2009
Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individualsE K Bijlsma, A C J Gijsbers, J H M Schuurs-Hoeijmakers, et al.Pageof 2