Showing results (351-360 of 2,549) with videos related to

Sort By:
Pageof 255
Neuropediatrics|December 7, 2007
Tyrosine hydroxylase deficiency presenting with a biphasic clinical courseT Giovanniello, V Leuzzi, C Carducci, et al.
Neuropediatrics|February 1, 1997
Low molecular weight storage material in infantile ceroid lipofuscinosis (CLN1)G Dawson, S Cho, A N Siakotos, et al.
Neuropediatrics|February 1, 1997
Sphingolipid activator proteins (SAPs) in neuronal ceroid lipofuscinoses (NCL)J Tyynelä, J Suopanki, M Baumann, et al.
Neuropediatrics|May 8, 2008
Confirmed primary HHV-6 infection in children with suspected encephalitisJ O Virtanen, E Herrgård, P Valmari, et al.
Neuropediatrics|May 8, 2008
Variable phenotype including Leigh syndrome with a 9185T>C mutation in the MTATP6 geneA-M Childs, T Hutchin, K Pysden, et al.
Neuropediatrics|January 24, 2006
Juvenile limb-girdle myasthenia gravisC Rodolico, C Pastura, S Sinicropi, et al.
Pageof 255