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2. A novel IMPDH1 mutation (Arg231Pro) in a family with a severe form of autosomal dominant retinitis pigmentosa. Grover S; Fishman GA; Stone EM Ophthalmology; 2004 Oct; 111(10):1910-6. PubMed ID: 15465556 [TBL] [Abstract][Full Text] [Related]
3. [Hereditary maculopathy in typical retinitis pigmentosa. Apropos of 40 cases]. Chachia N; Romdane K; Zaghdane M; Hadj Hamida FB; Khayrallah M; Haddad M Ophtalmologie; 1989; 3(1):67-8. PubMed ID: 2641075 [TBL] [Abstract][Full Text] [Related]
4. [Genetic aspects in pigmentary retinopathy]. Preoteasa D Oftalmologia; 1996; 40(2):137-44. PubMed ID: 8717081 [TBL] [Abstract][Full Text] [Related]
5. [Applicability of semi-automated kinetic perimetry (SKP) in the assessment of the visual field loss due to retinitis pigmentosa]. Nowomiejska K; Paetzold J; Krapp E; Rejdak R; Zarnowski T; Zagórski Z; Schiefer U Klin Oczna; 2004; 106(3 Suppl):500-2. PubMed ID: 15636249 [TBL] [Abstract][Full Text] [Related]
6. [Examinations of color vision in the differentiation of retinopathia pigmentosa]. Hammerstein W; Mecklenbeck W Klin Monbl Augenheilkd; 1983 Jan; 182(1):51-3. PubMed ID: 6855119 [TBL] [Abstract][Full Text] [Related]
7. Screen of the IMPDH1 gene among patients with dominant retinitis pigmentosa and clinical features associated with the most common mutation, Asp226Asn. Wada Y; Sandberg MA; McGee TL; Stillberger MA; Berson EL; Dryja TP Invest Ophthalmol Vis Sci; 2005 May; 46(5):1735-41. PubMed ID: 15851576 [TBL] [Abstract][Full Text] [Related]
8. [Distribution of the frequency of various Mendelian modes of inheritance in families with retinopathia pigmentosa. Results of an evaluation of the RP register of the Munster University Ophthalmology Clinic]. Gerding H; Busse H Ophthalmologe; 1994 Jun; 91(3):322-8. PubMed ID: 8086748 [TBL] [Abstract][Full Text] [Related]
14. A multicenter study of typical retinitis pigmentosa in Japan. Hayakawa M; Matsumura M; Ohba N; Matsui M; Fujiki K; Kanai A; Tamai M; Shiono T; Tokoro T; Akazawa Y Jpn J Ophthalmol; 1993; 37(2):156-64. PubMed ID: 8230840 [TBL] [Abstract][Full Text] [Related]
15. [A dissociation of thresholds between Goldmann kinetic perimetry and high-pass resolution perimetry in retinitis pigmentosa]. Tokuhisa T; Oyama K; Tamaki R; Kitahara K Nippon Ganka Gakkai Zasshi; 1992 Nov; 96(11):1429-32. PubMed ID: 1476073 [TBL] [Abstract][Full Text] [Related]
16. [Autosomal dominant transmission in retinitis pigmentosa]. Ghenoiu R Oftalmologia; 1993; 37(4):339-41. PubMed ID: 8286320 [TBL] [Abstract][Full Text] [Related]
18. [Genetic study of retinal pigmentary dystrophy (retinitis pigmentosa) in Japan]. Tanabe U Jinrui Idengaku Zasshi; 1972 Mar; 16(3):119-53. PubMed ID: 5065755 [No Abstract] [Full Text] [Related]
19. Genetic aspects of retinitis pigmentosa in China. Hu DN Am J Med Genet; 1982 May; 12(1):51-6. PubMed ID: 7091196 [TBL] [Abstract][Full Text] [Related]
20. Retinitis pigmentosa in the Navajo. Heckenlively J; Friederich R; Farson C; Pabalis G Metab Pediatr Ophthalmol; 1981; 5(3-4):201-6. PubMed ID: 7311662 [No Abstract] [Full Text] [Related] [Next] [New Search]