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The Journal of Pediatrics|May 29, 1998
Legg-Perthes disease in three siblings, two heterozygous and one homozygous for the factor V Leiden mutationR Gruppo, C J Glueck, E Wall, et al.Pediatrics|January 1, 1976
Pediatric familial type II hyperlipoproteinemia: therapy with diet and colestipol resinC J Glueck, R W Fallat, M Mellies, et al.Metabolism: Clinical and Experimental|October 1, 1980
Cholesterol-free diet and the physiologic hyperlipidemia of pregnancy in familial hypercholesterolemiaC J Glueck, C Christopher, R C Tsang, et al.Pediatrics|March 1, 1977
Therapy of familial hypercholesterolemia in childhood: diet and cholestyramine resin for 24 to 36 monthsC J Glueck, R C Tsang, R W Fallat, et al.Cranio : the Journal of Craniomandibular Practice|December 16, 1998
Exogenous estrogen may exacerbate thrombophilia, impair bone healing and contribute to development of chronic facial painC J Glueck, R E McMahon, J E Bouquot, et al.American Journal of Diseases of Children (1960)|January 1, 1975
Neonatal familial hypercholesterolemiaR C Tsnag, C J Glueck, R W Fallat, et al.The American Journal of Cardiology|July 1, 1992
Gemfibrozil-lovastatin therapy for primary hyperlipoproteinemiasC J Glueck, N Oakes, J Speirs, et al.Journal of Lipid Research|May 1, 1974
Quantitative analysis of cholesterol in 5 to 20 microliter of plasmaT T Ishikawa, J MacGee, J A Morrison, et al.Pediatrics|August 1, 1986
Safety and efficacy of long-term diet and diet plus bile acid-binding resin cholesterol-lowering therapy in 73 children heterozygous for familial hypercholesterolemiaC J Glueck, M J Mellies, M Dine, et al.Metabolism: Clinical and Experimental|November 1, 1976
Pediatric familial type III hyperlipoproteinemiaC J Glueck, R W Fallat, M J Mellies, et al.Pageof 23