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Journal Abstract Search

145 related items for PubMed ID: 4643533

  • 1. Prenatal Niemann-Pick disease: biochemical and histologic examination of a 19-gestational week fetus.
    Schneider EL, Ellis WG, Brady RO, McCulloch JR, Epstein CJ.
    Pediatr Res; 1972 Sep; 6(9):720-9. PubMed ID: 4643533
    [No Abstract] [Full Text] [Related]

  • 2. In utero diagnosis of Niemann-Pick disease.
    Epstein CJ, Brady RO, Schneider EL, Bradley RM, Shapiro D.
    Am J Hum Genet; 1971 Sep; 23(5):533-5. PubMed ID: 4328491
    [No Abstract] [Full Text] [Related]

  • 3. Infantile (type II) Gaucher's disease: in utero diagnosis and fetal pathology.
    Schneider EL, Ellis WG, Brady RO, McCulloch JR, Epstein CJ.
    J Pediatr; 1972 Dec; 81(6):1134-9. PubMed ID: 4674572
    [No Abstract] [Full Text] [Related]

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  • 8. Chemical and biochemical studies in human fetuses affected with Niemann-Pick disease type A.
    Klibansky C, Chazan S, Schoenfeld A, Abramovici A.
    Clin Chim Acta; 1979 Feb 01; 91(3):243-50. PubMed ID: 761400
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  • 9. Prenatal diagnosis of G M1 -gangliosidosis.
    Lowden JA, Cutz E, Conen PE, Rudd N, Doran TA.
    N Engl J Med; 1973 Feb 01; 288(5):225-8. PubMed ID: 4345063
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  • 12. [A case of sphingolipidosis with accumulation of various lipids in different organs and multiple enzymatic changes in the liver].
    Giardini O, Cardi E, Castro M, Cao M.
    Minerva Pediatr; 1975 Dec 15; 27(39):2188-94. PubMed ID: 172772
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  • 13. A practical chromogenic procedure for the detection of homozygotes and heterozygous carriers of Niemann-Pick disease.
    Gal AE, Brady RO, Hibbert SR, Pentchev PG.
    N Engl J Med; 1975 Sep 25; 293(13):632-6. PubMed ID: 239343
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  • 14. Sphingomyelin and glucocerebroside of spleen in cases of Gaucher's and Niemann-Pick's diseases.
    Taketomi T, Yamakawa T.
    Jpn J Exp Med; 1967 Oct 25; 37(5):505-9. PubMed ID: 5303496
    [No Abstract] [Full Text] [Related]

  • 15. Infantile Niemann-Pick disease. A chemical study with isolation and characterization of membranous cytoplasmic bodies and myelin.
    Kamoshita S, Aron AM, Suzuki K, Suzuki K.
    Am J Dis Child; 1969 Apr 25; 117(4):379-94. PubMed ID: 5773407
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  • 16. [Prenatal diagnosis of Sandhoff's disease (GM2-gangliosidosis, type 2)].
    Harzer K, Stengel-Rutkowski S, Gley EO, Albert A, Murken JD, Zahn V, Henkel KP.
    Dtsch Med Wochenschr; 1975 Jan 17; 100(3):106-8. PubMed ID: 234374
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  • 17. Lipid analysis of a case of GM1-generalized gangliosidosis.
    Abe T, Okada R.
    Jpn J Exp Med; 1972 Dec 17; 42(6):543-51. PubMed ID: 4540906
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  • 19. [Lipidosis--metabolism].
    Taketomi T.
    Tanpakushitsu Kakusan Koso; 1969 Mar 17; 14(4):346-56. PubMed ID: 4183081
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  • 20. Metabolism of fatty acid-labeled cerebroside sulfate in cultured cells from controls and metachromatic leukodystrophy patients. Use in the prenatal identification of a false positive fetus.
    Kudoh T, Sattler M, Malmstrom J, Bitter MA, Wenger DA.
    J Lab Clin Med; 1981 Nov 17; 98(5):704-14. PubMed ID: 6117597
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