BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

125 related articles for article (PubMed ID: 7206914)

  • 1. Electroretinographic changes in a case of spino-cerebellar degeneration (SCD).
    Stanescu B; Evrard P; Michiels J; Lyon G
    Metab Pediatr Ophthalmol; 1980; 4(4):221-3. PubMed ID: 7206914
    [No Abstract]   [Full Text] [Related]  

  • 2. [Study on the relationship of spino-cerebellar hereditary degeneration and progressive muscular atrophy].
    Ramelli E; Mapelli G
    Riv Neurobiol; 1972; 18(2):101-34. PubMed ID: 4681150
    [No Abstract]   [Full Text] [Related]  

  • 3. [Epilepsy and hereditary spino-cerebellar degeneration].
    Gayral L; Gayral J
    J Genet Hum; 1969 May; 17(1):127-36. PubMed ID: 4980118
    [No Abstract]   [Full Text] [Related]  

  • 4. Electroretinographic intensity-response function in retinal disease.
    Wu LZ; Massof RW; Starr SJ
    Chin Med J (Engl); 1985 Apr; 98(4):250-6. PubMed ID: 3924519
    [No Abstract]   [Full Text] [Related]  

  • 5. [A heredo-familial spinocerebellar degeneration with slow eye movements--a study of five cases (author's transl)].
    Kanehisa Y; Suda M; Yagi K; Beppu H; Uono M
    Rinsho Shinkeigaku; 1979 Apr; 19(4):209-16. PubMed ID: 445925
    [No Abstract]   [Full Text] [Related]  

  • 6. Hereditary spino-cerebellar degeneration and Ramsay-Hunt disease.
    Penneau D; Bigorgne JC; Fressinaud-Masdefeix L
    Cah Med; 1974 Feb; 15(2):93-6. PubMed ID: 4848865
    [No Abstract]   [Full Text] [Related]  

  • 7. [Anomalies of ocular saccades in a case of familial spino-cerebellar degeneration].
    Perenin MT; Prablanc C
    Rev Electroencephalogr Neurophysiol Clin; 1974; 4(3):489-94. PubMed ID: 4470972
    [No Abstract]   [Full Text] [Related]  

  • 8. [Genetic aspects of some spino-cerebellar degenerations].
    Badiu G
    Stud Cercet Neurol; 1969; 14(5):311-24. PubMed ID: 4906012
    [No Abstract]   [Full Text] [Related]  

  • 9. The coexistence of age-related macular degeneration and retinitis pigmentosa in three unrelated families.
    Sarraf D; Salib DM; Jain A; Quiram PA
    Semin Ophthalmol; 2007; 22(3):155-61. PubMed ID: 17763236
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Transplantation of retinal pigment epithelial, photoreceptor and other cells as treatment for retinal degeneration.
    Litchfield TM; Whiteley SJ; Lund RD
    Exp Eye Res; 1997 May; 64(5):655-66. PubMed ID: 9245894
    [No Abstract]   [Full Text] [Related]  

  • 11. A case of familial spinocerebellar degeneration with hypobetalipoproteinemia.
    Korula J; Namasivayam RK; Shadangi TN; Reddy PK; Raman PT
    Neurol India; 1976 Mar; 24(1):41-5. PubMed ID: 179026
    [No Abstract]   [Full Text] [Related]  

  • 12. Low-frequency damped electroretinographic wavelets in young asymptomatic patients with dominant retinitis pigmentosa: a new electroretinographic finding.
    Lam BL; Liu M; Hamasaki DI
    Ophthalmology; 1999 Jun; 106(6):1109-13. PubMed ID: 10366078
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Application of Fourier analysis to the smooth pursuit eye movements in normal subjects and spino-cerebellar degeneration].
    Hatakeyama M
    Nippon Ganka Gakkai Zasshi; 1982; 86(6):607-12. PubMed ID: 7136966
    [No Abstract]   [Full Text] [Related]  

  • 14. An autosomal recessive disorder with posterior column ataxia and retinitis pigmentosa.
    Higgins JJ; Morton DH; Patronas N; Nee LE
    Neurology; 1997 Dec; 49(6):1717-20. PubMed ID: 9409377
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Heredo - familial spinocerebellar degeneration with slow eye movements--another variety of olivopontocerebellar degeneration.
    Wadia NH
    Neurol India; 1977 Sep; 25(3):147-60. PubMed ID: 613260
    [No Abstract]   [Full Text] [Related]  

  • 16. Autosomal dominant system degeneration in Portuguese families of the Azores Islands. A new genetic disorder involving cerebellar, pyramidal, extrapyramidal and spinal cord motor functions.
    Coutinho P; Andrade C
    Neurology; 1978 Jul; 28(7):703-9. PubMed ID: 566869
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Joseph disease in India--report of two families.
    Jain S; Maheshwari MC
    J Neurogenet; 1986 Jan; 3(1):61-73. PubMed ID: 3958821
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hereditary diseases of the retina in a study of blind and partially sighted.
    Odland M
    Birth Defects Orig Artic Ser; 1982; 18(6):657-67. PubMed ID: 7171782
    [No Abstract]   [Full Text] [Related]  

  • 19. A brief review of retinitis pigmentosa and the identified retinitis pigmentosa genes.
    Phelan JK; Bok D
    Mol Vis; 2000 Jul; 6():116-24. PubMed ID: 10889272
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Evaluation of some clinical parameters in patients with retinitis pigmentosa in relationship to the type of inheritance].
    Zalewska R; Midro AT; Stankiewicz A; Mariak Z; Proniewska-Skretek E; Sobolewski P
    Klin Oczna; 1999; 101(1):29-32. PubMed ID: 10401211
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.