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Archives of Disease in Childhood|September 1, 1988
Juvenile myoclonic epilepsyM J Clement, S J WallaceDevelopmental Medicine and Child Neurology|October 1, 1990
EEG monitoring of therapy for neonatal seizuresV F Hakeem, S J WallaceHuman Genetics|April 4, 2000
Compound heterozygous mutations in the flavoprotein gene of the respiratory chain complex II in a patient with Leigh syndromeB Parfait, D Chretien, A Rötig, et al.Developmental Medicine and Child Neurology|October 1, 1990
A survey of adolescents with epilepsyM J Clement, S J WallaceNeuropediatrics|August 1, 1992
Kearns-Sayre syndrome with sideroblastic anemia: molecular investigationsI Nelson, G Bonne, F Degoul, et al.Biochemical and Biophysical Research Communications|October 28, 1994
Chronic progressive external ophthalmoplegia is associated with a novel mutation in the mitochondrial tRNA(Asn) geneP Seibel, J Lauber, T Klopstock, et al.Histochemistry|January 1, 1990
Immunohistochemical demonstration of fibre type-specific isozymes of cytochrome c oxidase in human skeletal muscleN Romero, C Marsac, M Fardeau, et al.Annales De Medecine Interne|January 1, 1980
[Alopecia, chronic candidodis, mental retardation and repeated ketoacidosic comas curable by biotin administration: multiple carboxylases deficiency (author's transl)]A Munnich, J M Saudubray, H Ogier, et al.Neurology|April 1, 1987
Phosphorus NMR spectroscopy study of muscular enzyme deficiencies involving glycogenolysis and glycolysisD Duboc, P Jehenson, S Tran Dinh, et al.Developmental Medicine and Child Neurology|September 1, 1990
Rapid anti-epileptic drug assayM Cosgrove, S Pople, S J WallacePageof 15