Manifestations of Inherited Disorders of Bilirubin Glucuronidation During Infancy and Childhood

Author:

Chowdhury Namita Roy,Ilan Yaron,Chowdhury Jayanta Roy

Publisher

Humana Press

Reference28 articles.

1. Roy Chowdhury J, Jansen PLM. Metabolism of bilirubin. In: Zakim D, Boyer TD, eds. Hepatology: a textbook of liver disease, 3rd ed. Saunders, Philadelphia, 1996, pp. 323–347.

2. Roy Chowdhury J, Roy Chowdhury N, Arias IM. Hereditary jaundice and disorders of bilirubin metabolism. In: Sciver, Boudet, Sly, Valle, eds. The metabolic and molecular bases of inherited disease, 7th ed. McGraw Hill, New York, 1995, pp. 2161–2208.

3. Crigler JF, Najjar VA. Congenital familial non-hemolytic jaundice with kernicterus. Pediatrics 1952; 10:169.

4. Wolkoff AW, Roy Chowdhury J, et al. Crigler-Najjar syndrome (Type I) in an adult male. Gastroenterology 1979;76:840–848.

5. Arias IM, Gartner LM, Cohen M, Benezzer J, Levi AJ. Chronic nonhemolytic unconjugated hyperbilirubine-mia with glucuronyltransferase deficiency: Clinical, biochemical, pharmacologic, and genetic evidence for heterogeneity. Am J Med 1969;47:395.

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