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Logo of procrsmedFormerly medchtJournal of the Royal Society of MedicineProceedings of the Royal Society of Medicine
 
Proc R Soc Med. 1971 February; 64(2): 185–186.
PMCID: PMC1812459

Fibroblast culture and inherited neurological diseases.

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Full text is available as a scanned copy of the original print version. Get a printable copy (PDF file) of the complete article (382K), or click on a page image below to browse page by page. Links to PubMed are also available for Selected References.
 
 

Selected References

These references are in PubMed. This may not be the complete list of references from this article.
  • Danes BS, Bearn AG. Hurler's syndrome: demonstration of an inherited disorder of connective tissue in cell culture. Science. 1965 Aug 27;149(3687):987–989. [PubMed]
  • Foley KM, Danes BS, Bearn AG. White blood cell cultures in genetic studies on the human mucopolysaccharidoses. Science. 1969 Apr 25;164(3878):424–426. [PubMed]
  • Fratantoni JC, Hall CW, Neufeld EF. The defect in Hurler's and Hunter's syndromes: faulty degradation of mucopolysaccharide. Proc Natl Acad Sci U S A. 1968 Jun;60(2):699–706. [PubMed]
  • Ho MW, O'Brien JS. Hurler's syndrome: deficiency of a specific beta galactosidase isoenzyme. Science. 1969 Aug 8;165(3893):611–613. [PubMed]
  • KROOTH RS, WEINBERG AN. Properties of galactosemic cells in culture. Biochem Biophys Res Commun. 1960 Nov;3:518–524. [PubMed]
  • MacBrinn MC, Okada S, Ho MW, Hu CC, O'Brien JS. Generalized gangliosidosis: impaired cleavage of galactose from a mucopolysaccharide and a glycoprotien. Science. 1969 Feb 28;163(3870):946–947. [PubMed]
  • Matalon R, Dorfman A. Acid mucopolysaccharides in cultured human fibroblasts. Lancet. 1969 Oct 18;2(7625):838–841. [PubMed]
  • Matalon R, Dorfman A, Dawson G, Sweeley CC. Glycolipid and mucopolysaccharide abnormality in fibroblasts of fabry's disease. Science. 1969 Jun 27;164(3887):1522–1523. [PubMed]
  • Nadler HL, Wodnicki JM, Swae MA, O'Flynn ME. Cultivated amniotic-fluid cells and fibroblasts derived from families with cystic fibrosis. Lancet. 1969 Jul 12;2(7611):84–85. [PubMed]
  • Steinberg D, Herndon JH, Jr, Uhlendorf BW, Mize CE, Avigan J, Milne GW. Refsum's disease: nature of the enzyme defect. Science. 1967 Jun 30;156(3783):1740–1742. [PubMed]
  • Swift MR, Finegold MJ. Myotonic muscular dystrophy: abnormalities in fibroblast culture. Science. 1969 Jul 18;165(3890):294–295. [PubMed]
  • Taysi K, Kistenmacher ML, Punnett HH, Mellman WJ. Limitations of metachromasia as a diagnostic aid in pediatrics. N Engl J Med. 1969 Nov 13;281(20):1108–1111. [PubMed]
  • Uhlendorf BW, Mudd SH. Cystathionine synthase in tissue culture derived from human skin: enzyme defect in homocystinuria. Science. 1968 May 31;160(3831):1007–1009. [PubMed]

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