Showing results (171-180 of 194) with videos related to
Sort By:
Pageof 20
Annals of Neurology|October 1, 1982
Dopaminergic dsyfunction in Tourette syndromeH S Singer, I J Butler, L E Tune, et al.Journal of Child Neurology|July 1, 1993
Proton magnetic resonance imaging and spectroscopic studies of the pathogenesis and treatment of juvenile dermatomyositisJ M Slopis, E F Jackson, P A Narayana, et al.The New England Journal of Medicine|October 10, 1985
Reduction of biogenic amine levels in the Rett syndromeH Y Zoghbi, A K Percy, D G Glaze, et al.Neurology|August 1, 1984
Short-latency somatosensory evoked potentials in the management of patients with achondroplasiaF W Nelson, W D Goldie, J T Hecht, et al.Archives of Neurology|May 18, 2001
Neurologic and psychiatric manifestations in a family with a mutation in exon 2 of the guanosine triphosphate-cyclohydrolase geneH Hahn, M R Trant, M J Brownstein, et al.The Journal of Pediatrics|November 1, 1976
Hyperphenylalaninemia due to dihydropteridine reductase deficiency. Assay of the enzyme in fibroblasts from affected infants, heterozygotes, and in normal amniotic fluid cellsS Milstien, N A Holtzman, M E O'Flynn, et al.The New England Journal of Medicine|July 19, 1984
Progressive neurologic deterioration and renal failure due to storage of glutamyl ribose-5-phosphateJ C Williams, I J Butler, H S Rosenberg, et al.Annals of Neurology|July 1, 1988
Neurological basis of respiratory complications in achondroplasiaF W Nelson, J T Hecht, W A Horton, et al.Journal of Applied Physiology (Bethesda, Md. : 1985)|November 1, 1990
Proton magnetic resonance of exercise-induced water changes in gastrocnemius muscleL K Fotedar, J M Slopis, P A Narayana, et al.Magnetic Resonance Imaging|March 1, 1989
In vivo muscle magnetic resonance spectroscopy in a family with mitochondrial cytopathy: a defect in fat metabolismP A Narayana, J M Slopis, E F Jackson, et al.Pageof 20