Literature DB >> 6796913

Possible carnitine requirement of the newborn and the effect of genetic disease on the carnitine requirement.

P R Borum.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1981        PMID： 6796913     DOI： 10.1111/j.1753-4887.1981.tb06722.x

Source DB:  PubMed          Journal:  Nutr Rev        ISSN： 0029-6643            Impact factor:   7.110


× No keyword cloud information.
  4 in total

1.  Hypocarnitinaemia in Menkes disease.

Authors:  P Kamoun; M Mayer; D Rabier
Journal:  Eur J Pediatr       Date:  1989-08       Impact factor: 3.183

Review 2.  On the molecular etiology of decreased arachidonic (20:4n-6), docosapentaenoic (22:5n-6) and docosahexaenoic (22:6n-3) acids in Zellweger syndrome and other peroxisomal disorders.

Authors:  J P Infante; V A Huszagh
Journal:  Mol Cell Biochem       Date:  1997-03       Impact factor: 3.396

3.  Bioconversion of a L-carnitin precursor in a one- or two-phase system.

Authors:  G Bare; P Jacques; J B Hubert; R Rikir; P Thonart
Journal:  Appl Biochem Biotechnol       Date:  1991       Impact factor: 2.926

Review 4.  Normal vitamin requirements in neonates and infants.

Authors:  C J Bates
Journal:  J Inherit Metab Dis       Date:  1985       Impact factor: 4.982
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.