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Clinical Neurology and Neurosurgery|January 1, 1981
Neurologic manifestations of homocystinuriaH C Schoonderwaldt, G H Boers, J R Cruysberg, et al.European Journal of Pediatrics|May 14, 1998
Treatment and follow-up of children with cerebrotendinous xanthomatosisA F van Heijst, A Verrips, R A Wevers, et al.American Journal of Ophthalmology|December 22, 2000
Juvenile macular dystrophy associated with deficient activity of fatty aldehyde dehydrogenase in Sjögren-Larsson syndromeM A Willemsen, J R Cruysberg, J J Rotteveel, et al.American Journal of Ophthalmology|June 1, 1996
Autosomal dominant central areolar choroidal dystrophy caused by a mutation in codon 142 in the peripherin/RDS geneC B Hoyng, P Heutink, L Testers, et al.Cerebrovascular Diseases (Basel, Switzerland)|July 6, 2000
Prevalence of symptomatic intracranial aneurysm and ischaemic stroke in pseudoxanthoma elasticumJ S van den Berg, R C Hennekam, J R Cruysberg, et al.Acta Neuropathologica|August 12, 1999
Severe, non X-linked congenital microcephaly with absence of the pyramidal tracts in two siblingsH J ten Donkelaar, P Wesseling, B A Semmekrot, et al.Human Molecular Genetics|February 1, 1994
Localization of the gene for dominant cystoid macular dystrophy on chromosome 7pH Kremer, A Pinckers, B van den Helm, et al.American Journal of Human Genetics|June 12, 1999
The molecular basis of cystathionine beta-synthase deficiency in Dutch patients with homocystinuria: effect of CBS genotype on biochemical and clinical phenotype and on response to treatmentL A Kluijtmans, G H Boers, J P Kraus, et al.Archives of Neurology|April 18, 2000
Presence of diarrhea and absence of tendon xanthomas in patients with cerebrotendinous xanthomatosisA Verrips, B G van Engelen, R A Wevers, et al.American Journal of Medical Genetics|November 20, 1995
Clinical findings in obligate carriers of type I Usher syndromeM Wagenaar, B ter Rahe, A van Aarem, et al.Pageof 11