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J F de Rijk-van Andel

Showing results (1-10 of 16) with videos related to

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Neuropediatrics|February 1, 1992
EEG and evoked potentials in a series of 21 patients with lissencephaly type IJ F de Rijk-van Andel, W F Arts, A W de Weerd
Developmental Medicine and Child Neurology|August 1, 1990
Diagnostic features and clinical signs of 21 patients with lissencephaly type 1J F de Rijk-van Andel, W F Arts, P G Barth, et al.
Neuroradiology|January 1, 1991
Neuroimaging in lissencephaly type IJ F de Rijk-van Andel, M S van der Knaap, J Valk, et al.
Neuroepidemiology|January 1, 1991
Epidemiology of lissencephaly type IJ F de Rijk-van Andel, W F Arts, A Hofman, et al.
Developmental Medicine and Child Neurology|April 1, 1991
Clinical and chromosome studies of three patients with Smith-Magenis syndromeJ F de Rijk-van Andel, C E Catsman-Berrevoets, J O van Hemel, et al.
American Journal of Medical Genetics|September 1, 1991
DNA analysis in patients with lissencephaly type I and other cortical dysplasiasB A Oostra, J F de Rijk-van Andel, H J Eussen, et al.
Human Genetics|August 1, 1991
Isolated lissencephaly sequence associated with a microdeletion at chromosome 17p13J F De Rijk-van Andel, C E Catsman-Berrevoets, D J Halley, et al.
Clinical Chemistry|September 11, 1998
Biochemical hallmarks of tyrosine hydroxylase deficiencyC Bräutigam, R A Wevers, R J Jansen, et al.
Neurology|January 3, 2001
L-dopa-responsive infantile hypokinetic rigid parkinsonism due to tyrosine hydroxylase deficiencyJ F de Rijk-Van Andel, F J Gabreëls, B Geurtz, et al.
Human Genetics|August 14, 1998
A common point mutation in the tyrosine hydroxylase gene in autosomal recessive L-DOPA-responsive dystonia in the Dutch populationL P van den Heuvel, B Luiten, J A Smeitink, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Neuropediatrics|February 1, 1992
EEG and evoked potentials in a series of 21 patients with lissencephaly type IJ F de Rijk-van Andel, W F Arts, A W de Weerd
Developmental Medicine and Child Neurology|August 1, 1990
Diagnostic features and clinical signs of 21 patients with lissencephaly type 1J F de Rijk-van Andel, W F Arts, P G Barth, et al.
Neuroradiology|January 1, 1991
Neuroimaging in lissencephaly type IJ F de Rijk-van Andel, M S van der Knaap, J Valk, et al.
Neuroepidemiology|January 1, 1991
Epidemiology of lissencephaly type IJ F de Rijk-van Andel, W F Arts, A Hofman, et al.
Developmental Medicine and Child Neurology|April 1, 1991
Clinical and chromosome studies of three patients with Smith-Magenis syndromeJ F de Rijk-van Andel, C E Catsman-Berrevoets, J O van Hemel, et al.
American Journal of Medical Genetics|September 1, 1991
DNA analysis in patients with lissencephaly type I and other cortical dysplasiasB A Oostra, J F de Rijk-van Andel, H J Eussen, et al.
Human Genetics|August 1, 1991
Isolated lissencephaly sequence associated with a microdeletion at chromosome 17p13J F De Rijk-van Andel, C E Catsman-Berrevoets, D J Halley, et al.
Clinical Chemistry|September 11, 1998
Biochemical hallmarks of tyrosine hydroxylase deficiencyC Bräutigam, R A Wevers, R J Jansen, et al.
Neurology|January 3, 2001
L-dopa-responsive infantile hypokinetic rigid parkinsonism due to tyrosine hydroxylase deficiencyJ F de Rijk-Van Andel, F J Gabreëls, B Geurtz, et al.
Human Genetics|August 14, 1998
A common point mutation in the tyrosine hydroxylase gene in autosomal recessive L-DOPA-responsive dystonia in the Dutch populationL P van den Heuvel, B Luiten, J A Smeitink, et al.
Pageof 2