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. 1973 Jul 7;3(5870):28–29. doi: 10.1136/bmj.3.5870.28

Kidney transplantation in Fabry's disease.

F R Bühler, G Thiel, U C Dubach, F Enderlin, F Gloor, H Thölen
PMCID: PMC1587971  PMID: 4577717

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Selected References

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

  1. Clarke J. T., Guttmann R. D., Wolfe L. S., Beaudoin J. G., Morehouse D. D. Enzyme replacement therapy by renal allotransplantation in Fabry's disease. N Engl J Med. 1972 Dec 14;287(24):1215–1218. doi: 10.1056/NEJM197212142872402. [DOI] [PubMed] [Google Scholar]
  2. Desnick R. J., Simmons R. L., Allen K. Y., Woods J. E., Anderson C. F., Najarian J. S., Krivit W. Correction of enzymatic deficiencies by renal transplantation: Fabry's disease. Surgery. 1972 Aug;72(2):203–211. [PubMed] [Google Scholar]
  3. Dubach U. C., Enderlin F., Mannhart M. [Absent renal ceramide-trihexosidase activity in Fabry's disease]. Ger Med Mon. 1969 Jan;14(1):34–35. [PubMed] [Google Scholar]
  4. Philippart M., Franklin S. S., Gordon A. Reversal of an inborn sphingolipidosis (Fabry's disease) by kidney transplantation. Ann Intern Med. 1972 Aug;77(2):195–200. doi: 10.7326/0003-4819-77-2-195. [DOI] [PubMed] [Google Scholar]
  5. Philippart M., Sarlieve L., Manacorda A. Urinary glycolipids in Fabry's disease. Their examination in the detection of atypical variants and the pre-symptomatic state. Pediatrics. 1969 Feb;43(2):201–206. [PubMed] [Google Scholar]
  6. Vance D. E., Krivit W., Sweeley C. C. Concentrations of glycosyl ceramides in plasma and red cells in Fabry's disease, a glycolipid lipidosis. J Lipid Res. 1969 Mar;10(2):188–192. [PubMed] [Google Scholar]

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