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Genetic heterogeneity in familial idiopathic basal ganglia calcification (Fahr disease).
Oliveira JR, Spiteri E, Sobrido MJ, Hopfer S, Klepper J, Voit T, Gilbert J, Wszolek ZK, Calne DB, Stoessl AJ, Hutton M, Manyam BV, Boller F, Baquero M, Geschwind DH. Oliveira JR, et al. Among authors: voit t. Neurology. 2004 Dec 14;63(11):2165-7. doi: 10.1212/01.wnl.0000145601.88274.88. Neurology. 2004. PMID: 15596772
Hypoglycorrhachia: a simple clue, simply missed.
Willemsen MA, Verrips A, Verbeek MM, Voit T, Klepper J. Willemsen MA, et al. Among authors: voit t. Ann Neurol. 2001 May;49(5):685-6. Ann Neurol. 2001. PMID: 11357965 No abstract available.
Progressive dystonia in a 12-year-old boy.
Klepper J, Schaper J, Raca G, Coryell J, Das S, Hayflick SJ, Voit T. Klepper J, et al. Among authors: voit t. Eur J Paediatr Neurol. 2003;7(2):85-8. doi: 10.1016/s1090-3798(03)00019-9. Eur J Paediatr Neurol. 2003. PMID: 12697433
Autosomal dominant transmission of GLUT1 deficiency.
Klepper J, Willemsen M, Verrips A, Guertsen E, Herrmann R, Kutzick C, Flörcken A, Voit T. Klepper J, et al. Among authors: voit t. Hum Mol Genet. 2001 Jan 1;10(1):63-8. doi: 10.1093/hmg/10.1.63. Hum Mol Genet. 2001. PMID: 11136715
318 results