Literature DB >> 6016174

Hereditary tyrosinemia and tyrosyluria in a French Canadian geographic isolate.

C R Scriver, J Larochelle, M Silverberg.   

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Year:  1967        PMID： 6016174     DOI： 10.1001/archpedi.1967.02090160091008

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN： 0002-922X


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  6 in total

1.  Juvenile rheumatoid arthritis. Cellular hypersensitivity and selective IgA deficiency.

Authors:  R S Panush; N E Bianco; P H Schur; R E Rocklin; J R David; J S Stillman
Journal:  Clin Exp Immunol       Date:  1972-01       Impact factor: 4.330

2.  Hereditary tyrosinemia in a French Canadian isolate.

Authors:  C Laberge
Journal:  Am J Hum Genet       Date:  1969-01       Impact factor: 11.025

3.  Management of transient hyperphenylalaninemia and tyrosinemia in low birth weight Negro infants fed high protein diets.

Authors:  M L Watkins; E P Crump; S Hara
Journal:  J Natl Med Assoc       Date:  1971-07       Impact factor: 1.798

4.  Clinical features and diagnostic approach in type I tyrosinaemia in an infant with cytomegaly virus infection and bacterial sepsis.

Authors:  M Wabitsch; F Pohlandt; D Leupold; R Berger; E Mönch; E Heinze; W Teller
Journal:  Eur J Pediatr       Date:  1993-04       Impact factor: 3.183

5.  Genetic epidemiology of hereditary tyrosinemia in Quebec and in Saguenay-Lac-St-Jean.

Authors:  M De Braekeleer; J Larochelle
Journal:  Am J Hum Genet       Date:  1990-08       Impact factor: 11.025

6.  Case of hepatocellular carcinoma in a patient with hereditary tyrosinemia in the post-newborn screening era.

Authors:  Essam M Imseis; John S Bynon; Chad Thornhill
Journal:  World J Hepatol       Date:  2017-03-28
  6 in total

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