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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

177 related items for PubMed ID: 5878602

  • 21. 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
    [Abstract] [Full Text] [Related]

  • 22. An autopsy case of Laurence-Moon-Biedl syndrome with pituitary eosinophilic adenoma.
    Hiraki S, Tsutsumi A, Tsuboi S.
    Acta Pathol Jpn; 1971 Aug; 21(3):435-43. PubMed ID: 4330953
    [No Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27. The syndrome of Laurence-Moon-Bardet-Biedl and allied diseases in Switzerland. Clinical, genetic and epidemiological studies.
    Klein D, Ammann F.
    J Neurol Sci; 1969 Aug; 9(3):479-513. PubMed ID: 5367041
    [No Abstract] [Full Text] [Related]

  • 28. Ocular myopathy.
    Davidson SI.
    Trans Ophthalmol Soc U K (1962); 1970 Aug; 90():139-59. PubMed ID: 4933925
    [No Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32. Genetic counseling in blindness.
    Walker FA.
    Sight Sav Rev; 1969 Aug; 39(2):105-11. PubMed ID: 5350350
    [No Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34. Genetic and clinical characterization of a survey population with retinitis pigmentosa.
    Boughman JA, Caldwell RJ.
    Prog Clin Biol Res; 1982 Aug; 82():147-66. PubMed ID: 7111271
    [No Abstract] [Full Text] [Related]

  • 35. A case of the Laurence-Moon-Beidl syndrome showing atypical retinitis pigmentosa associated with macular dystrophy.
    TAYLOR C.
    Br J Ophthalmol; 1947 Apr; 31(4):211-5. PubMed ID: 20293694
    [No Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37. [A case of spinocerebellar ataxia with retinitis pigmentosa, deafness, seizure and EEG abnormality (author's transl)].
    Itoh J, Akiguchi I, Tanaka M, Nakamura S, Kameyama M.
    Rinsho Shinkeigaku; 1980 Jul; 20(7):577-83. PubMed ID: 7460428
    [No Abstract] [Full Text] [Related]

  • 38.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 39. Investigations into the aqueous humour dynamics in primary pigmentary degeneration of the retina.
    Kogbe OI, Follmann P.
    Ophthalmologica; 1975 Jul; 171(2):165-75. PubMed ID: 1153175
    [Abstract] [Full Text] [Related]

  • 40. Juvenile nephronophthisis associated with retinal pigmentary dystrophy, cerebellar ataxia, and skeletal abnormalities.
    Popović-Rolović M, Calić-Perisíc N, Bunjevacki G, Negovanović D.
    Arch Dis Child; 1976 Oct; 51(10):801-3. PubMed ID: 1008585
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 9.