Skip to main content
British Medical Journal logoLink to British Medical Journal
. 1972 Aug 19;3(5824):433–434.

Spongy change in the brain.

PMCID: PMC1785987  PMID: 4672053

Full text

PDF
433

Selected References

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

  1. ALVORD E. C., Jr, STEVENSON L. D., VOGEL F. S., ENGLE R. L., Jr Neuropathological findings in phenyl-pyruvic oligophrenia (phenyl-ketonuria). J Neuropathol Exp Neurol. 1950 Jul;9(3):298–310. doi: 10.1097/00005072-195007000-00004. [DOI] [PubMed] [Google Scholar]
  2. CHOU S. M., WAISMAN H. A. SPONGY DEGENERATION OF THE CENTRAL NERVOUS SYSTEM: CASE OF HOMOCYSTINURIA. Arch Pathol. 1965 Apr;79:357–363. [PubMed] [Google Scholar]
  3. Curley A., Kimbrough R. D., Hawk R. E., Nathenson G., Finberg L. Dermal absorption of hexochlorophane in infants. Lancet. 1971 Aug 7;2(7719):296–297. doi: 10.1016/s0140-6736(71)91337-7. [DOI] [PubMed] [Google Scholar]
  4. Gibbs C. J., Jr, Gajdusek D. C. Infection as the etiology of spongiform encephalopathy (Creutzfeldt-Jakob disease). Science. 1969 Sep 5;165(3897):1023–1025. doi: 10.1126/science.165.3897.1023. [DOI] [PubMed] [Google Scholar]
  5. Rushton D. I. Spongy degeneration of the white matter of the central nervous system associated with hyperglycinuria. J Clin Pathol. 1968 Jul;21(4):456–462. doi: 10.1136/jcp.21.4.456. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Solitare G. B., Shih V. E., Nelligan D. J., Dolan T. F., Jr Argininosuccinic aciduria: clinical, biochemical, anatomical and neuropathological observations. J Ment Defic Res. 1969 Sep;13(3):153–170. doi: 10.1111/j.1365-2788.1969.tb01076.x. [DOI] [PubMed] [Google Scholar]

Articles from British Medical Journal are provided here courtesy of BMJ Publishing Group

RESOURCES