Skip to main content
The British Journal of Ophthalmology logoLink to The British Journal of Ophthalmology
. 1963 Oct;47(10):620–631. doi: 10.1136/bjo.47.10.620

ERYTHROCYTIC ANOMALIES IN HEREDITARY VITREO-RETINAL DEGENERATION (DEGENERATIO HYALOIDEORETINALIS)*

A Kahán 1, I L Kahán 1, A Benkő 1, S Mindszenti 1
PMCID: PMC505860  PMID: 14198722

Full text

PDF
620

Images in this article

Selected References

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

  1. AKSOY M., ALPUSTUN H., DEVRIMEL H., PECEL N. The thalassaemia syndromes. II. Intermediate type of Cooley's anaemia. Study of a family. Acta Haematol. 1961 Mar;25:200–206. doi: 10.1159/000206533. [DOI] [PubMed] [Google Scholar]
  2. BASSEN F. A., KORNZWEIG A. L. Malformation of the erythrocytes in a case of atypical retinitis pigmentosa. Blood. 1950 Apr;5(4):381–387. [PubMed] [Google Scholar]
  3. BOEHRINGER H. R., DIETERLE P., LANDOLT E. [On the clinical manifestation and pathology of degeneratio hyaloideoretinalis hereditaria (Wagner)]. Ophthalmologica. 1960 Mar-Apr;139:330–338. doi: 10.1159/000303718. [DOI] [PubMed] [Google Scholar]
  4. CHOREMIS C., KYRIAKIDES V., PAPADAKIS E. Studies on the blood lipids and lipoproteins in thalassaemia and sickle cell anaemia. J Clin Pathol. 1961 Jul;14:361–364. doi: 10.1136/jcp.14.4.361. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. DRUEZ G., LAMY M., FREZAL J., POLONOVSKI J., REY J. [Acanthocytosis. Its relations to the congenital absence of beta-lipoproteins]. Presse Med. 1961 Jul 15;69:1546–1548. [PubMed] [Google Scholar]
  6. GIESER E. P., FALLS H. F. Hereditary retinoschisis. Am J Ophthalmol. 1961 Jun;51:1193–1200. doi: 10.1016/0002-9394(61)92457-6. [DOI] [PubMed] [Google Scholar]
  7. GOLDBERG C. A. A discontinuous buffer system for paper electrophoresis of human hemoglobins. Clin Chem. 1959 Oct;5:446–451. [PubMed] [Google Scholar]
  8. JAMPEL R. S., FALLS H. F. Atypical retinitis pigmentosa, acanthrocytosis, and heredodegenerative neuromuscular disease. AMA Arch Ophthalmol. 1958 Jun;59(6):818–820. doi: 10.1001/archopht.1958.00940070032002. [DOI] [PubMed] [Google Scholar]
  9. JONXIS J. H. Some remarks on hemoglobinopathies with particular reference to thalassemia. J Pediatr. 1961 Nov;59:765–776. doi: 10.1016/s0022-3476(61)80019-x. [DOI] [PubMed] [Google Scholar]
  10. KAHAN A., OLAH I. Ein Simultan-Adaptometer. Acta Med Acad Sci Hung. 1954;5(1-2):175–183. [PubMed] [Google Scholar]
  11. KLEIHAUER E., BETKE K. [Practical use of the demonstration of cells containing hemoglobin F in fixed blood smears]. Izv Mikrobiol Inst (Sofiia) 1960 Sep;1:292–295. [PubMed] [Google Scholar]
  12. KORNZWEIG A. L., BASSEN F. A. Retinitis pigmentosa, acanthrocytosis, and heredodegenerative neuromuscular disease. AMA Arch Ophthalmol. 1957 Aug;58(2):183–187. doi: 10.1001/archopht.1957.00940010195004. [DOI] [PubMed] [Google Scholar]
  13. KRISTOFFERSEN K. An improved method for the estimation of small quantities of alkali-resistant hemoglobin in blood. Scand J Clin Lab Invest. 1961;13:402–409. [PubMed] [Google Scholar]
  14. MIER M., SCHWARTZ S. O., BOSHES B. Acanthrocytosis, pigmentary degeneration of the retina and ataxic neuropathy: a genetically determined syndrome and associated metabolic disorder. Blood. 1960 Nov;16:1586–1608. [PubMed] [Google Scholar]
  15. Mann I., Macrae A. CONGENITAL VASCULAR VEILS IN THE VITREOUS. Br J Ophthalmol. 1938 Jan;22(1):1–10. doi: 10.1136/bjo.22.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. ROBINSON A. R., ROBSON M., HARRISON A. P., ZUELZER W. W. A new technique for differentiation of hemoglobin. J Lab Clin Med. 1957 Nov;50(5):745–752. [PubMed] [Google Scholar]
  17. RUDD C., EVANS P. J., PEENEY A. L. Ocular complications in thalassaemia minor. Br J Ophthalmol. 1953 Jun;37(6):353–358. doi: 10.1136/bjo.37.6.353. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. SINGER K., CHERNOFF A. I., SINGER L. Studies on abnormal hemoglobins. I. Their demonstration in sickle cell anemia and other hematologic disorders by means of alkali denaturation. Blood. 1951 May;6(5):413–428. [PubMed] [Google Scholar]
  19. SINGER K., FISHER B., PERLSTEIN M. A. Acanthrocytosis; a genetic erythrocytic malformation. Blood. 1952 Jun;7(6):577–591. [PubMed] [Google Scholar]
  20. SORSBY A., KLEIN M., GANN J. H., SIGGINS G. Unusual retinal detachment possibly sex-linked. Br J Ophthalmol. 1951 Jan;35(1):1–10. doi: 10.1136/bjo.35.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. ZAK B., DICKENMAN R. C., WHITE E. G., BURNETT H., CHERNEY P. J. Rapid estimation of free and total cholesterol. Am J Clin Pathol. 1954 Nov;24(11):1307–1315. doi: 10.1093/ajcp/24.11_ts.1307. [DOI] [PubMed] [Google Scholar]
  22. ZAK B., LUZ D. A., FISHER M. Determination of serum cholesterol. Am J Med Technol. 1957 Sep-Oct;23(5):283–287. [PubMed] [Google Scholar]

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

RESOURCES