Showing results (211-220 of 276) with videos related to
Sort By:
Pageof 28
Lancet (London, England)|July 30, 1994
Preliminary evidence from magnetic resonance imaging for reduction in disease activity after lymphocyte depletion in multiple sclerosisT Moreau, J Thorpe, D Miller, et al.Annals of Clinical Biochemistry|January 1, 1987
Bringing HELP to the clinical laboratory--use of an expert system to provide automatic interpretation of laboratory dataP D Clayton, R S Evans, T Pryor, et al.Diabetes|December 1, 1993
Early introduction of dairy products associated with increased risk of IDDM in Finnish children. The Childhood in Diabetes in Finland Study GroupS M Virtanen, L Räsänen, K Ylönen, et al.Journal of the American Academy of Dermatology|June 1, 1997
Adult pityriasis rubra pilaris: a 10-year case seriesB D Clayton, J L Jorizzo, M G Hitchcock, et al.Chemical Science|September 22, 2023
Synthesis and metalation of polycatechol nanohoops derived from fluorocycloparaphenylenesAshlyn A Kamin, Tara D Clayton, Claire E Otteson, et al.Chemical Science|November 9, 2022
Automated stopped-flow library synthesis for rapid optimisation and machine learning directed experimentationClaudio Avila, Carlo Cassani, Thierry Kogej, et al.Gynecologic Oncology|October 5, 2001
Safety and efficacy of low anterior en bloc resection as part of cytoreductive surgery for patients with ovarian cancerA Obermair, S Hagenauer, D Tamandl, et al.Molecular Pharmacology|June 1, 1985
Inhibition of utilization of hypoxanthine and guanine in cells treated with the carbocyclic analog of adenosine. Phosphates of carbocyclic nucleoside analogs as inhibitors of hypoxanthine (guanine) phosphoribosyltransferaseL L Bennett, R W Brockman, L M Rose, et al.Neurogenetics|February 7, 2001
Evidence that allelic variants of the spinocerebellar ataxia type 2 gene influence susceptibility to multiple sclerosisJ Chataway, S Sawcer, F Coraddu, et al.Neuromuscular Disorders : NMD|May 11, 2010
Drosophila indirect flight muscle specific Act88F actin mutants as a model system for studying congenital myopathies of the human ACTA1 skeletal muscle actin geneSarah E Haigh, Sheetal S Salvi, Maria Sevdali, et al.Pageof 28