Literature DB >> 5453458

Familial hypercarotinaemia and hypovitaminosis A.

D E Sharvill.   

Abstract

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Year:  1970        PMID： 5453458      PMCID： PMC1811589     

Source DB:  PubMed          Journal:  Proc R Soc Med        ISSN： 0035-9157


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  2 in total

1.  Enzymatic defect in Fabry's disease. Ceramidetrihexosidase deficiency.

Authors:  R O Brady; A E Gal; R M Bradley; E Martensson; A L Warshaw; L Laster
Journal:  N Engl J Med       Date:  1967-05-25       Impact factor: 91.245

2.  [Keratodermal state with lowered serum level of vitamin A and hypercarotinemia].

Authors:  E Frenk
Journal:  Dermatologica       Date:  1966
  2 in total
  3 in total

1.  Perspective: Advancing Understanding of Population Nutrient-Health Relations via Metabolomics and Precision Phenotypes.

Authors:  Stephanie Andraos; Melissa Wake; Richard Saffery; David Burgner; Martin Kussmann; Justin O'Sullivan
Journal:  Adv Nutr       Date:  2019-11-01       Impact factor: 8.701

Review 2.  Genetic Variations of Vitamin A-Absorption and Storage-Related Genes, and Their Potential Contribution to Vitamin A Deficiency Risks Among Different Ethnic Groups.

Authors:  Masako Suzuki; Meika Tomita
Journal:  Front Nutr       Date:  2022-04-28

3.  Carotenemia in mentally retarded children. I. Incidence and etiology.

Authors:  H Patel; H G Dunn; B Tischer; A K McBurney; E Hach
Journal:  Can Med Assoc J       Date:  1973-04-07       Impact factor: 8.262
  3 in total

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