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European Journal of Nuclear Medicine and Molecular Imaging|January 15, 2005
O-(2-[18F]fluorethyl)-L-tyrosine PET in the clinical evaluation of primary brain tumoursM Weckesser, K J Langen, C H Rickert, et al.British Journal of Haematology|March 1, 1996
Resistance to activated protein C (APCR) in children with venous or arterial thromboembolismU Nowak-Göttl, H G Koch, I Aschka, et al.Neuroscience Letters|March 6, 1998
Absence of mutations in peripheral myelin protein-22, myelin protein zero, and connexin 32 in autosomal recessive Dejerine-Sottas syndromeF Stögbauer, P Young, H Wiebusch, et al.Annals of Neurology|October 20, 1998
Progressive myoclonus epilepsy and mitochondrial myopathy associated with mutations in the tRNA(Ser(UCN)) geneM Jaksch, T Klopstock, G Kurlemann, et al.Journal of Inherited Metabolic Disease|March 18, 2015
A new case of UDP-galactose transporter deficiency (SLC35A2-CDG): molecular basis, clinical phenotype, and therapeutic approachK Dörre, M Olczak, Y Wada, et al.Neuropediatrics|June 10, 2005
SCN1A mutation analysis in myoclonic astatic epilepsy and severe idiopathic generalized epilepsy of infancy with generalized tonic-clonic seizuresK Ebach, H Joos, H Doose, et al.Neurology|July 16, 2008
KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromesB A Neubauer, S Waldegger, J Heinzinger, et al.Archives of Disease in Childhood|October 21, 2010
Limbic encephalitis in children and adolescentsE Haberlandt, T Bast, A Ebner, et al.Neurology|June 11, 2003
Rapsyn N88K is a frequent cause of congenital myasthenic syndromes in European patientsJ S Müller, G Mildner, W Müller-Felber, et al.Neurology|December 17, 1998
Centrotemporal spikes in families with rolandic epilepsy: linkage to chromosome 15q14B A Neubauer, B Fiedler, B Himmelein, et al.Pageof 9