Literature DB >> 14159408

ERYTHROCYTIC GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE LEVELS IN HEPATIC CIRRHOSIS.

M M FISHER, S SPEAR, E SAMOLS, S SHERLOCK.   

Abstract

Entities:  

Keywords:  DIAGNOSIS, LABORATORY; ENZYME TESTS; ERYTHROCYTES; GALACTOSEMIA; HEPATOLENTICULAR DEGENERATION; LIVER CIRRHOSIS; LIVER DISEASES; NUCLEOTIDYLTRANSFERASES

Mesh：

Substances：

Year:  1964        PMID： 14159408      PMCID： PMC1552199          DOI： 10.1136/gut.5.2.170

Source DB:  PubMed          Journal:  Gut        ISSN： 0017-5749            Impact factor:   23.059


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  11 in total

1.  ACTIVE 'JUVENILE' CIRRHOSIS CONSIDERED AS PART OF A SYSTEMIC DISEASE AND THE EFFECT OF CORTICOSTEROID THERAPY.

Authors:  A E READ; S SHERLOCK; C V HARRISON
Journal:  Gut       Date:  1963-12       Impact factor: 23.059

2.  Galactosemia: a study of twenty-seven kindreds in North America.

Authors:  F A WALKER; D Y HSIA; H M SLATIS; A G STEINBERG
Journal:  Ann Hum Genet       Date:  1962-05       Impact factor: 1.670

3.  A study of the genetics of galactosaemia.

Authors:  V SCHWARZ; A R WELLS; A HOLZEL; G M KOMROWER
Journal:  Ann Hum Genet       Date:  1961-12       Impact factor: 1.670

4.  The genetic mechanism of galactosaemia.

Authors:  K HUGH-JONES; A L NEWCOMB; D Y HSIA
Journal:  Arch Dis Child       Date:  1960-12       Impact factor: 3.791

5.  Galactosemia.

Authors:  G N DONNELL; W R BERGREN; R S CLELAND
Journal:  Pediatr Clin North Am       Date:  1960-05       Impact factor: 3.278

6.  Variability in the clinical manifestations of galactosemia.

Authors:  D Y HSIA; F A WALKER
Journal:  J Pediatr       Date:  1961-12       Impact factor: 4.406

7.  Galactosemia, a congenital defect in a nucleotide transferase.

Authors:  H M KALCKAR; E P ANDERSON; K J ISSELBACHER
Journal:  Biochim Biophys Acta       Date:  1956-04

8.  A specific enzymatic assay for the diagnosis of congenital galactosemia. I. The consumption test.

Authors:  E P ANDERSON; H M KALCKAR; K KURAHASHI; K J ISSELBACHER
Journal:  J Lab Clin Med       Date:  1957-09

9.  A PROCEDURE FOR DETECTING CARRIERS OF GALACTOSEMIA.

Authors:  R K Bretthauer; R G Hansen; G Donnell; W R Bergren
Journal:  Proc Natl Acad Sci U S A       Date:  1959-03       Impact factor: 11.205

10.  FAMILIAL HEPATIC COPPER STORAGE DISEASE: A VARIANT OF WILSON'S DISEASE.

Authors:  M M FISHER; S SHERLOCK
Journal:  Arch Dis Child       Date:  1964-02       Impact factor: 3.791
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