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. 1974 Jul;49(7):579–581. doi: 10.1136/adc.49.7.579

Severe neonatal citrullinaemia.

D M Danks, P Tippett, G Zentner
PMCID: PMC1648906  PMID: 4854268

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Danks D. M. Management of newborn babies in whom serious metabolic illness is anticipated. Arch Dis Child. 1974 Jul;49(7):576–578. doi: 10.1136/adc.49.7.576. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Scott-Emuakpor A., Higgins J. V., Kohrman A. F. Citrullinemia: a new case, with implications concerning adaptation to defective urea synthesis. Pediatr Res. 1972 Jul;6(7):626–633. [PubMed] [Google Scholar]
  3. Tippett P. A., Danks D. M. Screening for aminoaciduria: a critical evaluation of four techniques and a survey of a mentally retarded population. Aust Paediatr J. 1972 Oct;8(5):255–263. doi: 10.1111/j.1440-1754.1972.tb01834.x. [DOI] [PubMed] [Google Scholar]
  4. Wick H., Bachmann C., Baumgartner R., Brechbühler T., Colombo J. P., Wiesmann U., Mihatsch M. J., Ohnacker H. Variants of citrullinaemia. Arch Dis Child. 1973 Aug;48(8):636–641. doi: 10.1136/adc.48.8.636. [DOI] [PMC free article] [PubMed] [Google Scholar]

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