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A Verrips

Showing results (31-40 of 38) with videos related to

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Brain : a Journal of Neurology|August 4, 1999
Spinal xanthomatosis: a variant of cerebrotendinous xanthomatosisA Verrips, G J Nijeholt, F Barkhof, 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|July 26, 2006
Distal spinal muscular atrophy as a major feature in adult-onset ataxia telangiectasiaJ A P Hiel, B G M van Engelen, C M R Weemaes, 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.
Journal of Medical Genetics|May 17, 2005
POMT2 mutations cause alpha-dystroglycan hypoglycosylation and Walker-Warburg syndromeJ van Reeuwijk, M Janssen, C van den Elzen, et al.
American Journal of Human Genetics|May 29, 2000
Aicardi-Goutières syndrome displays genetic heterogeneity with one locus (AGS1) on chromosome 3p21Y J Crow, A P Jackson, E Roberts, 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 4

Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
Brain : a Journal of Neurology|August 4, 1999
Spinal xanthomatosis: a variant of cerebrotendinous xanthomatosisA Verrips, G J Nijeholt, F Barkhof, 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|July 26, 2006
Distal spinal muscular atrophy as a major feature in adult-onset ataxia telangiectasiaJ A P Hiel, B G M van Engelen, C M R Weemaes, 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.
Journal of Medical Genetics|May 17, 2005
POMT2 mutations cause alpha-dystroglycan hypoglycosylation and Walker-Warburg syndromeJ van Reeuwijk, M Janssen, C van den Elzen, et al.
American Journal of Human Genetics|May 29, 2000
Aicardi-Goutières syndrome displays genetic heterogeneity with one locus (AGS1) on chromosome 3p21Y J Crow, A P Jackson, E Roberts, 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 4