Deficiency of Fumarylacetoacetase in the Acute Form of Hereditary Tyrosinemia with Reference to Prenatal Diagnosis-Reference-Cited by-同舟云学术

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Deficiency of Fumarylacetoacetase in the Acute Form of Hereditary Tyrosinemia with Reference to Prenatal Diagnosis

Published:1983 Issue: Volume: Page:223-235
ISSN:
Container-title:Pediatric Liver Disease
language:
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Author:

Melançon S. B.,Gagné R.,Grenier A.,Lescault A.,Dallaire L.,Laberge C.,Potier M.

Publisher

Springer US

Link

http://link.springer.com/content/pdf/10.1007/978-1-4684-4385-1_21.pdf

Reference23 articles.

1. LA DUBN,GJESSINGLR: Tyrosinosis and Tyrosinemia. InThe Metabolic Basis of Inherited Disease, 4th Edition. JB Stanbury, JB Wyngaarden, DS Fredrickson (eds). McGraw Hill Co., N.Y. 1978. pp. 256–267.

2. WADMANSK,SPRANGFJ, VANMAASJW,KETTINGD: An exceptional case of tyrosinosis.J Ment Defic Res 12; 269–281, 1968.

3. LOUISWJ,PITTDD,DAVIESH: Biochemical studies in a patient with tyrosinosis.Aust NZ Jl Med 4:281–286, 1974.

4. HARRIESJT,SEAKINSJWT,ERSSERRS,LLOYDJK: Recovery after dietary treatment of an infant with features of tyrosinosis.Arch Dis Child 44:258–267, 1969.

5. JAISWALRB,BHAII,NATHN,NATHMC: Tyrosinosis, clinical, radiological and biochemical aspects.Indian Pediat 6: 1–17, 1969.

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1. Amniotic Fluid;Genetic Disorders and the Fetus;1986

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