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Neuromuscular Disorders : NMD|January 15, 2020
X-linked infantile spinal muscular atrophy (SMAX2) caused by novel c.1681G>A substitution in the UBA1 gene, expanding the phenotypeNiamh Shaughnessy, Eva B Forman, Declan O'Rourke, et al.Proceedings. AMIA Symposium|February 5, 2002
Using narrative reports to support a digital libraryE A Mendonça, J J Cimino, S B JohnsonTopics in Health Information Management|April 8, 1993
Full-text document storage and retrieval in a clinical information systemR V Sideli, S B Johnson, P D ClaytonJournal of Abnormal Child Psychology|June 1, 1984
A psychometric study of the family adaptability and cohesion evaluation scalesB B Alexander, S B Johnson, R L CarterProceedings. Symposium on Computer Applications in Medical Care|January 1, 1994
Accessing the Columbia Clinical RepositoryS B Johnson, G Hripcsak, J Chen, et al.The Journal of Clinical Psychiatry|December 1, 1986
A case of massive rhabdomyolysis following molindone administrationS B Johnson, W A Alvarez, J P FreinharThe Journal of Clinical Investigation|April 1, 1994
Direct quantification of apparent binding indices from quinidine-induced in vivo conduction delay in canine myocardiumF N Haugland, S B Johnson, D L PackerThe Journal of Trauma|July 1, 1992
Early criteria predictive of prolonged mechanical ventilationS B Johnson, P A Kearney, D E BarkerChemistry and Physics of Lipids|March 1, 1988
Determination of ester carbonyl 18O/16O ratios in phospholipids by gas chromatography-mass spectrometryP C Schmid, S B Johnson, H H SchmidJournal of Pediatric Psychology|April 26, 2000
Response to hypo- and hyperglycemia in adolescents with type I diabetesS B Johnson, A R Perwien, J H SilversteinPageof 98