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Journal Abstract Search

116 related items for PubMed ID: 4123897

  • 21. The regulation of plasma lipoprotein concentrations as affected in human mutants.
    Fredrickson DS.
    Proc Natl Acad Sci U S A; 1969 Nov; 64(3):1138-46. PubMed ID: 5264144
    [No Abstract] [Full Text] [Related]

  • 22. [Polyneuropathy: neuropathies due to metabolic deficiencies].
    Takeuchi H, Tarui S.
    Nihon Rinsho; 1982 Nov; 40(7):1488-93. PubMed ID: 6184496
    [No Abstract] [Full Text] [Related]

  • 23. Progressive ophthalmoplegia. Report of cases.
    Rosenberg RN, Schotland DL, Lovelace RE, Rowland LP.
    Arch Neurol; 1968 Oct; 19(4):362-76. PubMed ID: 4175668
    [No Abstract] [Full Text] [Related]

  • 24. [Pigmentary retinopathy of Bassen-Kornzweig syndrome. Clinical, biological and electrophysiological study of 2 cases].
    Weber M, Annonier P, Coumaros D, Willemin B, Bronner A.
    Bull Soc Ophtalmol Fr; 1988 Mar; 88(3):423-6. PubMed ID: 3063411
    [No Abstract] [Full Text] [Related]

  • 25. [Familial analphalipoproteinemia (Tangier disease)].
    Kummer H, Laissue J, Spiess H, Pflugshaupt R, Bucher U.
    Schweiz Med Wochenschr; 1968 Mar 16; 98(11):406-12. PubMed ID: 5700506
    [No Abstract] [Full Text] [Related]

  • 26.
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  • 27. [Polyneuropathy in familial analphalipoproteinemia (Tangier disease)].
    Spiess H, Ludin HP, Kummer H.
    Nervenarzt; 1969 Apr 16; 40(4):191-3. PubMed ID: 5362054
    [No Abstract] [Full Text] [Related]

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  • 30. [Concept and systematization of the hypolipemic syndromes].
    Schüller A.
    Rev Clin Esp; 1974 Mar 15; 132(5):399-404. PubMed ID: 4133922
    [No Abstract] [Full Text] [Related]

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  • 32. Abetalipoproteinemia and the eye.
    Carr RE.
    Birth Defects Orig Artic Ser; 1976 Mar 15; 12(3):385-408. PubMed ID: 782598
    [No Abstract] [Full Text] [Related]

  • 33. A-beta-lipoproteinaemia. Ocular involvement in a Danish case.
    Ehlers N, Hansen HJ.
    Acta Ophthalmol (Copenh); 1981 Oct 15; 59(5):747-55. PubMed ID: 7315226
    [Abstract] [Full Text] [Related]

  • 34. Refsum disease due to the splice-site mutation c.135-2A>G before exon 3 of the PHYH gene, diagnosed eight years after detection of retinitis pigmentosa.
    Finsterer J, Regelsberger G, Voigtländer T.
    J Neurol Sci; 2008 Mar 15; 266(1-2):182-6. PubMed ID: 17905308
    [Abstract] [Full Text] [Related]

  • 35. Congenital absence of beta-lipoproteins.
    LAMY M, FREZAL J, POLONOVSKI J, DRUEZ G, REY J.
    Pediatrics; 1963 Feb 15; 31():277-89. PubMed ID: 13928363
    [No Abstract] [Full Text] [Related]

  • 36. Atypical retinitis pigmentosa in familial hypobetalipoproteinemia.
    Yee RD, Herbert PN, Bergsma DR, Biemer JJ.
    Am J Ophthalmol; 1976 Jul 15; 82(1):64-71. PubMed ID: 180811
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  • 39. Abetalipoproteinemia: metabolic, endocrine, and electron-microscopic investigations.
    Sperling MA, Hengstenberg F, Yunis E, Kenny FM, Drash AL.
    Pediatrics; 1971 Jul 15; 48(1):91-102. PubMed ID: 5561886
    [No Abstract] [Full Text] [Related]

  • 40. Editorials on recent advances: Retinitis pigmentosa and retinol-binding protein.
    Gouras P, Chader G.
    Invest Ophthalmol; 1974 Apr 15; 13(4):239-42. PubMed ID: 4818807
    [No Abstract] [Full Text] [Related]

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