𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Colour vision in retinitis pigmentosa

✍ Scribed by A. Pinckers; A. Aarem; J. E. E. Keunen


Publisher
Springer Netherlands
Year
1993
Tongue
English
Weight
293 KB
Volume
17
Category
Article
ISSN
0165-5701

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Flicker electroretinogram in retinitis p
✍ R. W. Massof; M. A. Johnson; J. S. Sunness; C. Perry; D. Finkelstein πŸ“‚ Article πŸ“… 1986 πŸ› Springer-Verlag 🌐 English βš– 642 KB
Recording neuromagnetic fields in retini
✍ B. Schmidt; T. Blum πŸ“‚ Article πŸ“… 1985 πŸ› Springer-Verlag 🌐 English βš– 210 KB

After stimulation of the left and right half-fields, it is possible to record contralateral visually evoked neuromagnetic fields (VEF) without any reference to the size of the half-field stimulus display. The test reacts extremely sensitively upon each shifting of the half field into the periphery t

Rhodopsin mutations in autosomal dominan
✍ Mai Al-Maghtheh; Cheryl Gregory; Chris Inglehearn; Alison Hardcastle; Shomi Bhat πŸ“‚ Article πŸ“… 1993 πŸ› John Wiley and Sons 🌐 English βš– 605 KB

Retinitis pigmentosa is an inherited progressive disease which is a major cause of blindness in western communities. It can be inherited as an autosomal dominant, autosomal recessive, or X-linked recessive disorder. In the autosomal dominant form (adRP), which comprises about 25% of total cases, app

Clinical and genetic heterogeneity in re
✍ Josseline Kaplan; Dominique Bonneau; Jean FrΓ©zal; Arnold Munnich; Jean-Louis Duf πŸ“‚ Article πŸ“… 1990 πŸ› Springer 🌐 English βš– 733 KB

The clinical course of defective vision and blindness has been investigated in relation to different modes of genetic transmission in a large series of 93 families with retinitis pigmentosa (RP). For autosomal dominant RP, two clinical subtypes could be distinguished according to the delay in macula