Primary tapetoretinal dystrophies as the cause of blindness and impaired vision in the republic of Croatia

Acta Clinica Croatica

Volumn 41, Issue 1, 2002, Pages 23-27

  Novak Lauš, Katia ^a   Kukulj, Suzana ^a   Zorić Geber, Mia ^a   Bastaić, Ojdana ^a  

^a SESTRE MILOSRDNICE UNIVERSITY HOSPITAL   (Croatia)

Author keywords

Blindness; Impaired vision; Retinitis pigmentosa

Indexed keywords

ADAPTOMETRY; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; AUTOSOMAL RECESSIVE INHERITANCE; BLINDNESS; CLINICAL FEATURE; COLOR VISION; CONTROLLED STUDY; CROATIA; DISEASE SEVERITY; ELECTRORETINOGRAPHY; FAMILY HISTORY; FEMALE; GENE MUTATION; GENETIC ASSOCIATION; GEOGRAPHIC DISTRIBUTION; HUMAN; INCIDENCE; MAJOR CLINICAL STUDY; MALE; MEDICAL RECORD; ONSET AGE; OPHTHALMOSCOPY; REGISTER; RETINITIS PIGMENTOSA; SLIT LAMP; TAPETORETINAL DEGENERATION; VISION TEST; VISUAL ACUITY; VISUAL FIELD; VISUAL IMPAIRMENT;

EID: 0036227395     PISSN: 03539466     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (13)

1. Epidemiologija sljepoée i slabovidnosti u Zagrebu
2. Introduction to genetics in ophthalmology, value of family studies
3. Mutations in a novel retina-specific gene cause autosomal dominant retinitis pigmentosa
4. Update on the molecular genetics of retinitis pigmentosa
5. Bolesti pigmentnog epitela i žilnice
6. Familial occurrence of retinitis punctata albescens and congenital sensorineural deafness
7. Retinitis pigmentosa: A report of experiences
8. Epidemiologie der blindheit in Deutschland
9. National survey of blindness and low vision in the Gambia: Results
10. Bolesti pigmentnog epitela i žilnice