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The American Journal of Gastroenterology|February 1, 1976
Clinical observations on the biliary system in cystic fibrosisJ N Isenberg, P R L'Heureux, W J Warwick, et al.AJR. American Journal of Roentgenology|June 1, 1977
Gallbladder disease in cystic fibrosisP R L'heureux, J N Isenberg, H L Sharp, et al.The Journal of Pediatrics|May 1, 1975
Aspartylglucosaminuria: psychomotor retardation masquerading as a mucopolysaccharidosisJ N Isenberg, H L SharpHuman Pathology|July 1, 1976
Aspartylglucosaminuria: unique biochemical and ultrastructural characteristicsJ N Isenberg, H L SharpThe American Review of Respiratory Disease|April 1, 1976
The glycoprotein-degrading potential of peripheral leukocytes in cystic fibrosisJ N Isenberg, S J Sahlstrom, H L SharpThe American Journal of Medicine|September 1, 1976
Immunodeficiency, xanthomas and obstructive liver diseaseJ N Isenberg, R F Hanson, G C Williams, et al.The Journal of Clinical Investigation|September 1, 1975
The metabolism of 3alpha, 7alpha, 12alpha-trihydorxy-5beta-cholestan-26-oic acid in two siblings with cholestasis due to intrahepatic bile duct anomalies. An apparent inborn error of cholic acid synthesisR F Hanson, J N Isenberg, G C Williams, et al.Pediatric Radiology|December 4, 1978
Rickets as a complication of intravenous hyperalimentation in infantsD H Binstadt, P R L'HeureuxPostgraduate Medicine|December 1, 1987
Diet for cystic fibrosis. Nutritional requirements and prescriptionsW J WarwickPageof 14