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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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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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