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Journal Abstract Search

119 related items for PubMed ID: 13928363

  • 1.
    ; . PubMed ID:
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  • 2. CONGENITAL BETA-LIPOPROTEIN DEFICIENCY: AN HEREDITARY DISORDER INVOLVING A DEFECT IN THE ABSORPTION AND TRANSPORT OF LIPIDS.
    ISSELBACHER KJ, SCHEIG R, PLOTKIN GR, CAULFIELD JB.
    Medicine (Baltimore); 1964 May; 43():347-61. PubMed ID: 14168744
    [No Abstract] [Full Text] [Related]

  • 3. CELIAC SYNDROME, RETINAL DYSTROPHY, ACANTHOCYTOSIS, WITHOUT DEFECT OF BETA LIPOPROTEIN.
    TOLENTINO P, SPIRITO L, JANNUZZI C.
    Ann Paediatr; 1964 May; 203():178-86. PubMed ID: 14212872
    [No Abstract] [Full Text] [Related]

  • 4.
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  • 5. A-BETA-LIPOPROTEINAEMIA.
    FORSYTH CC, LLOYD JK, FOSBROOKE AS.
    Arch Dis Child; 1965 Feb; 40(209):47-51. PubMed ID: 14259271
    [No Abstract] [Full Text] [Related]

  • 6. The night-blinding disorders.
    Carr RE.
    Int Ophthalmol Clin; 1969 Feb; 9(4):971-1003. PubMed ID: 4101337
    [No Abstract] [Full Text] [Related]

  • 7.
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  • 8. A-BETA-LIPOPROTEINAEMIA WITH SPECIAL REFERENCE TO THE VISUAL DEFECT.
    WOLFF OH, LLOYD JK, TONKS EL.
    Exp Eye Res; 1964 Dec; 3():439-42. PubMed ID: 14282999
    [No Abstract] [Full Text] [Related]

  • 9. Pigmentary retinopathy associated with metabolic defects.
    Levy IS.
    Trans Ophthalmol Soc U K (1962); 1972 Dec; 92():285-7. PubMed ID: 4123897
    [No Abstract] [Full Text] [Related]

  • 10. [OLIGOPHRENIA, CONGENITAL CATARACT, RETINITIS PIGMENTOSA, CEREBELLAR ATAXIA, NEUROGENIC AMYOTROPHIA. OBSERVATIONS ON 3 FAMILIAL CASES AND COMPARISON WITH THE MARINESCO-SJOGREN'S SYNDROME].
    CALVI LA.
    Sist Nerv; 1963 Dec; 15():189-98. PubMed ID: 14073896
    [No Abstract] [Full Text] [Related]

  • 11. [Pathogenesis of acanthocytosis].
    REY J, FREZAL J, LAMY M.
    Nouv Rev Fr Hematol; 1963 Dec; 3():60-2. PubMed ID: 13981884
    [No Abstract] [Full Text] [Related]

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  • 14. INCUBATION HEMOLYSIS AND RED CELL METABOLISM IN ACANTHOCYTOSIS.
    SIMON ER, WAYS P.
    J Clin Invest; 1964 Jul; 43(7):1311-21. PubMed ID: 14192511
    [No Abstract] [Full Text] [Related]

  • 15. Retinitis Pigmentosa in Oliver McFarlane Syndrome.
    Kumari S, Bagraniya V, Kumar V.
    Ophthalmol Retina; 2023 Nov; 7(11):1009. PubMed ID: 37318400
    [No Abstract] [Full Text] [Related]

  • 16.
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  • 17. [Case of congenital hearing impairment with retinitis pigmentosa & mental deficiency].
    BOCHENEK Z, KUS J.
    Otolaryngol Pol; 1958 Nov; 12(2):181-6. PubMed ID: 13600821
    [No Abstract] [Full Text] [Related]

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  • 19. [The congenital absence of beta-lipoproteins].
    LAMY M, FREZAL J, POLONOVSKI J, REY J.
    Presse Med (1893); 1961 Jul 08; 69():1511-4. PubMed ID: 13758598
    [No Abstract] [Full Text] [Related]

  • 20.
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