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J F de Rijk-van Andel

Showing results (11-20 of 16) with videos related to

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Journal of Inherited Metabolic Disease|July 17, 1999
A review of biochemical and molecular genetic aspects of tyrosine hydroxylase deficiency including a novel mutation (291delC)R A Wevers, J F de Rijk-van Andel, C Bräutigam, et al.
Annals of Neurology|June 14, 2000
Clinical and biochemical characteristics of congenital disorder of glycosylation type Ic, the first recognized endoplasmic reticulum defect in N-glycan synthesisS Grünewald, T Imbach, K Huijben, et al.
Neurology|August 2, 2008
Prognostic factors after a first attack of inflammatory CNS demyelination in childrenR F Neuteboom, M Boon, C E Catsman Berrevoets, 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.
Journal of Neurology|February 22, 2012
Incidence of acquired demyelinating syndromes of the CNS in Dutch children: a nationwide studyI A Ketelslegers, C E Catsman-Berrevoets, R F Neuteboom, et al.
Journal of Neurology|March 24, 2018
Incidence and outcome of acquired demyelinating syndromes in Dutch children: update of a nationwide and prospective studyC L de Mol, Y Y M Wong, E D van Pelt, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Journal of Inherited Metabolic Disease|July 17, 1999
A review of biochemical and molecular genetic aspects of tyrosine hydroxylase deficiency including a novel mutation (291delC)R A Wevers, J F de Rijk-van Andel, C Bräutigam, et al.
Annals of Neurology|June 14, 2000
Clinical and biochemical characteristics of congenital disorder of glycosylation type Ic, the first recognized endoplasmic reticulum defect in N-glycan synthesisS Grünewald, T Imbach, K Huijben, et al.
Neurology|August 2, 2008
Prognostic factors after a first attack of inflammatory CNS demyelination in childrenR F Neuteboom, M Boon, C E Catsman Berrevoets, 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.
Journal of Neurology|February 22, 2012
Incidence of acquired demyelinating syndromes of the CNS in Dutch children: a nationwide studyI A Ketelslegers, C E Catsman-Berrevoets, R F Neuteboom, et al.
Journal of Neurology|March 24, 2018
Incidence and outcome of acquired demyelinating syndromes in Dutch children: update of a nationwide and prospective studyC L de Mol, Y Y M Wong, E D van Pelt, et al.
Pageof 2