These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

148 related articles for article (PubMed ID: 8086748)

  • 1. [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]  

  • 2. Epidemiology of retinitis pigmentosa in the Valencian community (Spain).
    Nájera C; Millán JM; Beneyto M; Prieto F
    Genet Epidemiol; 1995; 12(1):37-46. PubMed ID: 7713399
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Retinitis pigmentosa in Spain. The Spanish Multicentric and Multidisciplinary Group for Research into Retinitis Pigmentosa.
    Ayuso C; Garcia-Sandoval B; Najera C; Valverde D; Carballo M; Antiñolo G
    Clin Genet; 1995 Sep; 48(3):120-2. PubMed ID: 8556816
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Complicated cataracts in various forms of retinitis pigmentosa. Type and incidence].
    Auffarth GU; Tetz MR; Krastel H; Blankenagel A; Völcker HE
    Ophthalmologe; 1997 Sep; 94(9):642-6. PubMed ID: 9410231
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. [Genetic heterogeneity of retinitis pigmentosa].
    Krawczyński MR; Pecold K
    Klin Oczna; 1994 Jan; 96(1):24-9. PubMed ID: 8078270
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [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]  

  • 8. A genetic analysis of retinitis pigmentosa.
    Shanker J; Ramesh A
    Indian J Ophthalmol; 1993 Apr; 41(1):23-5. PubMed ID: 8225518
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Retinitis pigmentosa in Puerto Rico.
    Tous HM; Izquierdo NJ
    P R Health Sci J; 2006 Dec; 25(4):315-8. PubMed ID: 17550097
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Problems in detecting etiological heterogeneity in genetic disease illustrated with retinitis pigmentosa.
    Beaty TH; Boughman JA
    Am J Med Genet; 1986 Jul; 24(3):493-504. PubMed ID: 3728568
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Assessment of clinical variables and counseling needs in patients with retinitis pigmentosa.
    Boughman JA; Caldwell RJ
    Am J Med Genet; 1982 Jun; 12(2):185-93. PubMed ID: 7102723
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Retinitis pigmentosa genetics: a study in Indian population.
    Vinchurkar MS; Sathye SM; Dikshit M
    Indian J Ophthalmol; 1996 Jun; 44(2):77-82. PubMed ID: 8916593
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [The incidence of Usher's syndrome and its clinical types].
    Bereketoğlu M; Avşar EU; Turan O; Afrashi F; Apaydin F
    Kulak Burun Bogaz Ihtis Derg; 2002; 9(1):15-20. PubMed ID: 12122620
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Indications and prognosis of cataract surgery in patients with retinitis pigmentosa].
    Auffarth GU; Tetz MR; Krastel H; Blankenagel A; Völcker HE
    Ophthalmologe; 1996 Apr; 93(2):168-76. PubMed ID: 8652984
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Tapeto-retinal degeneration in four Norwegian counties, II. Diagnostic evaluation of 407 relatives and genetic evaluation of 87 families.
    Grøndahl J
    Clin Genet; 1986 Jan; 29(1):17-41. PubMed ID: 3948428
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Retinitis pigmentosa in Ontario - a survey.
    Macrae WG
    Birth Defects Orig Artic Ser; 1982; 18(6):175-85. PubMed ID: 7171753
    [No Abstract]   [Full Text] [Related]  

  • 17. Is there genetic heterogeneity in Usher's syndrome?
    Matthews TW; Poliquin J; Mount J; MacFie D
    J Otolaryngol; 1987 Mar; 16(2):61-6. PubMed ID: 3599157
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Autosomal recessive retinitis pigmentosa is associated with mutations in RP1 in three consanguineous Pakistani families.
    Riazuddin SA; Zulfiqar F; Zhang Q; Sergeev YV; Qazi ZA; Husnain T; Caruso R; Riazuddin S; Sieving PA; Hejtmancik JF
    Invest Ophthalmol Vis Sci; 2005 Jul; 46(7):2264-70. PubMed ID: 15980210
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Nonsyndromic retinitis pigmentosa is highly prevalent in the Jerusalem region with a high frequency of founder mutations.
    Sharon D; Banin E
    Mol Vis; 2015; 21():783-92. PubMed ID: 26261414
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A new clinical classification for Usher's syndrome based on a new subtype of Usher's syndrome type I.
    Otterstedde CR; Spandau U; Blankenagel A; Kimberling WJ; Reisser C
    Laryngoscope; 2001 Jan; 111(1):84-6. PubMed ID: 11192904
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.