8
Views
26
CrossRef citations to date
0
Altmetric
Original Article

Autosomal dominant cone dystrophy-cerebellar atrophy (ADCoCA) (modified ADCA Harding II)

, , &
Pages 261-275 | Accepted 20 Jul 1990, Published online: 08 Jul 2009

References

  • Arden GB, Carter RM, Hogg CR, Powell DJ, Ernst JK, Clover GM, Lyness AL, Quinlan MP. Rod and cone activity in patients with dominantly inherited retinitis pigmentosa: comparisons between psychophysical and electroretinographic measurements. Br J Ophthalmol 1983; 67: 405–418
  • Berson E, Gouras P, Gunkel R. Progressive cone-rod degeneration. Arch Ophthalmol 1968; 80: 68–74
  • Gouras P, Carr RE. Electrophysiological studies in early retinitis pigmentosa. Arch Ophthalmol 1964; 72: 104–110
  • Verougstraete C, Toussaint D. Dégénéiescence tapéto-réinienne avec ataxie cértéelleuse: étude clinique chez plusieurs membres d'une meme famille. Bull Soc Belg Ophtalmol 1973; 164: 285–295
  • Gass JD. Alias of Macular Diseases. CV Mosby, St Louis 1977; Vol 1: 192
  • Franceschetti A, Francois J, Babel J. Les Hérédédégénérescences Chorioritiniennes (Dégénérescences Tapéto-rétiniennes). Masson, Paris 1963; II: 1061–1073
  • Neetens A. Innere Neuroretinopathie mit Nachtblindheit und generalisierter peripherer Neuropathie. Klin Mb! Augen-heilk 1988; 192: 157–162
  • Neetens A. The heterogeneity of nightblindness and tapetoretinal degeneration. A review. Boll Oculist 1988; 1(67)25–39, suppl
  • François J, Neetens A. Bardet-Biedl syndrome and keratoconus. Ophthalm Paed Genet 1983; 2: 119–122
  • Harding AE. The Hereditary Ataxia and Related Disorders. Clinical Neurology and Neurosurgery Monographs. Churchill Livingstone, Edinburgh/London 1984; 1: 266
  • Bergstedt M, Johansson S, Muller R. Hereditary spastic ataxia with central retinal degeneration and vestibular impairment. A clinical report on a family. Neurology 1962; 12: 124–132
  • Bjork A, Lindblom U, Wadensten L. Retinal degeneration in hereditary ataxia. J Neurol Neurosurg Psychiat 1956; 19: 186–193
  • Boudin G, Barbizet J, Le Henaff MY. Hérédo-ataxie céérbelleuse avec amblyopie et paralysie de la verticals du regard chez la mere et l'enfant. Rev Neurol (Paris) 1952; 87: 330–335
  • Carpenter S, Schumacher GA. Familial infantile cerebellar atrophy associated with retinal degeneration. Arch Neurol 1966; 14: 82–94
  • Colan RV, Snead OC, Ceballos R. Olivopontocerebellar atrophy in children: a report of seven cases in two families. Ann Neurol 1981; 10: 355–363
  • Foster JB, Ingram TTS. Familial cerebro-macular degeneration and ataxia. J Neurol Neurosurg Psychiat 1962; 25: 63–68
  • Harding AE. The clinical features and classification of the late onset autosomal dominant cerebellar ataxias: a study of eleven families, including descendants of the 'Drew family of Walworth'. Brain 1982; 105: 1–28
  • Havener WH. Cerebellar-macular abiotrophy. Arch Ophthalmol 1951; 45: 40–43
  • Jampel RS, Okazaki H, Bernstein H. Ophthalmoplegia and retinal degeneration associated with spinocerebellar ataxia. Arch Ophthalmol 1961; 66: 247–259
  • Landau WM, Gitt JJ. Hereditary spastic paraplegia and hereditary ataxia. A family demonstrating a variety of phenoty pic manifestations. Arch Neurol Psychiat 1951; 66: 346–354
  • Weiner LP, Konigsmark BW. Hereditary disease of the cerebellar parenchyma. Birth Defects Orig Art Ser 1971; 7: 192–196
  • Weiner LP, Konigsmark BW, Stoll J, Magladery JW. Hereditary olivopontocerebellar atrophy with retinal degeneration. Report of a family through 6 generations. Arch Neurol 1967; 16: 364–376
  • Krill AE, Deutmann AF. Dominant macular degenerations. The cone dystrophies. Am J Ophthalmol 1972; 73: 352–361
  • Woodworth JA, Beckett RS, Netsky MG. A composite of hereditary ataxias. Arch Int Med 1959; 104: 594–606
  • Stanescu B, Evrard P, Michiels J, Lyon G. Electroretinographic changes in a case of spinocerebellar degeneration (SCD). Metabol Pediatr Ophthalmol 1980; 4: 221–224

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.