Literature DB >> 20788750

ANNOTATIONS.

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Abstract

Year:  1959        PMID： 20788750      PMCID： PMC1992211     

Source DB:  PubMed          Journal:  Br Med J        ISSN： 0007-1447


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  6 in total

1.  Wilson's disease; an inborn error of metabolism with multiple manifestations.

Authors:  A G BEARN
Journal:  Am J Med       Date:  1957-05       Impact factor: 4.965

2.  An inborn error of metabolism with the urinary excretion of alpha-hydroxy-butyric acid and phenylpyruvic acid.

Authors:  A J SMITH; L B STRANG
Journal:  Arch Dis Child       Date:  1958-04       Impact factor: 3.791

3.  A disease, probably hereditary characterised by severe mental deficiency and a constant gross abnormality of aminoacid metabolism.

Authors:  J D ALLAN; D C CUSWORTH; C E DENT; V K WILSON
Journal:  Lancet       Date:  1958-01-25       Impact factor: 79.321

4.  Non-Addisonian megaloblastic anemia; the intermediate megaloblast in the differential diagnosis of pernicious and related anemias.

Authors:  H FUDENBERG; S ESTREN
Journal:  Am J Med       Date:  1958-08       Impact factor: 4.965

5.  Hereditary pellagra-like skin rash with temporary cerebellar ataxia, constant renal amino-aciduria, and other bizarre biochemical features.

Authors:  D N BARON; C E DENT; H HARRIS; E W HART; J B JEPSON
Journal:  Lancet       Date:  1956-09-01       Impact factor: 79.321

6.  Sporadic non-endemic goitrous cretinism; hereditary transmission.

Authors:  J H HUTCHISON; E M MCGIRR
Journal:  Lancet       Date:  1956-06-30       Impact factor: 79.321
  6 in total

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