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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

100 related articles for article (PubMed ID: 3702277)

  • 1. [Lipid storage diseases (lipidoses): genetic, biochemical and clinico-chemical aspects].
    Bernheimer H; Molzer B
    Klin Padiatr; 1986; 198(2):84-8. PubMed ID: 3702277
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Ganglioside storage diseases.
    O'Brien JS
    Adv Hum Genet; 1972; 3():39-98. PubMed ID: 4268938
    [No Abstract]   [Full Text] [Related]  

  • 3. Prenatal diagnosis of inborn errors of metabolism.
    Mahoney MJ
    Clin Perinatol; 1979 Sep; 6(2):255-73. PubMed ID: 391465
    [No Abstract]   [Full Text] [Related]  

  • 4. Haematological aspects of lipid storage diseases.
    Brady RO
    Acta Haematol Pol; 1977; 8(2):103-12. PubMed ID: 407769
    [No Abstract]   [Full Text] [Related]  

  • 5. Infantile metachromatic leukodystrophy. Confirmation of a prenatal diagnosis.
    Leroy JG; Van Elsen AF; Martin JJ; Dumon JE; Hulet AE; Okada S; Navarro C
    N Engl J Med; 1973 Jun; 288(26):1365-9. PubMed ID: 4707419
    [No Abstract]   [Full Text] [Related]  

  • 6. The prenatal diagnosis of inborn errors of metabolism.
    Milunsky A; Littlefield JW
    Annu Rev Med; 1972; 23():57-76. PubMed ID: 4264784
    [No Abstract]   [Full Text] [Related]  

  • 7. Acid lipase in cultured fibroblasts: cholesterol ester storage disease.
    Beaudet AL; Lipson MH; Ferry GD; Nichols BL
    J Lab Clin Med; 1974 Jul; 84(1):54-61. PubMed ID: 4833843
    [No Abstract]   [Full Text] [Related]  

  • 8. Enzyme defects in the sphingolipidoses and their application to diagnosis.
    Brady RO
    Ann Clin Lab Sci (1971); 1972; 2(4):285-94. PubMed ID: 4342099
    [No Abstract]   [Full Text] [Related]  

  • 9. Biochemical basis of late-onset neurolipidoses.
    Conzelmann E; Sandhoff K
    Dev Neurosci; 1991; 13(4-5):197-204. PubMed ID: 1817024
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Detection of Fabry hemizygotes and heterozygotes by measurement of -galactosidase in urine.
    Rietra PJ; Tager JM; de Groot WP
    Clin Chim Acta; 1972 Aug; 40(1):229-35. PubMed ID: 5056633
    [No Abstract]   [Full Text] [Related]  

  • 11. Enzymes in amniotic fluid.
    Watkins BF; Bermes EW
    Ann Clin Lab Sci; 1977; 7(3):231-40. PubMed ID: 193424
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Ganglioside-storage diseases.
    O'Brien JS
    N Engl J Med; 1971 Apr; 284(15):893-6. PubMed ID: 5549832
    [No Abstract]   [Full Text] [Related]  

  • 13. [Prenatal diagnosis of inborn errors of metabolism. 155 cases (author's transl)].
    Boué J; Nicolas H; Cheruy C; Couillin P; Boué A
    Nouv Presse Med; 1982 Mar; 11(13):979-83. PubMed ID: 7070985
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Ichthyosis and neutral lipid storage disease.
    Williams ML; Koch TK; O'Donnell JJ; Frost PH; Epstein LB; Grizzard WS; Epstein CJ
    Am J Med Genet; 1985 Apr; 20(4):711-26. PubMed ID: 3993689
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal genetic diagnosis (second of three parts).
    Milunsky A; Littlefield JW; Kanfer JN; Kolodny EH; Shih VE; Atkins L
    N Engl J Med; 1970 Dec; 283(26):1441-7. PubMed ID: 4098222
    [No Abstract]   [Full Text] [Related]  

  • 16. Gm2-gangliosidosis: studies in cultured fibroblasts.
    Kolodny EH; Milunsky A; Sheng GS
    Birth Defects Orig Artic Ser; 1973 Mar; 9(2):130-5. PubMed ID: 4611525
    [No Abstract]   [Full Text] [Related]  

  • 17. Lactosylceramidosis: lactosylceramide galactosyl hydrolase deficiency and accumulation of lactosylceramide in cultured skin fibroblasts.
    Dawson G; Matalon R; Stein AO
    J Pediatr; 1971 Sep; 79(3):423-9. PubMed ID: 5567965
    [No Abstract]   [Full Text] [Related]  

  • 18. Ganglioside GM2 storage diseases: hexosaminidase deficiencies in cultured fibroblasts.
    Okada S; Veath ML; Leroy J; O'Brien JS
    Am J Hum Genet; 1971 Jan; 23(1):55-61. PubMed ID: 5581981
    [No Abstract]   [Full Text] [Related]  

  • 19. Glycosidases in normal human leukocytes and abnormalities in G M1 -gangliosidosis.
    Hindman J; Cotlier E
    Clin Chem; 1972 Sep; 18(9):971-5. PubMed ID: 5052099
    [No Abstract]   [Full Text] [Related]  

  • 20. Ichthyosis and neutral lipid storage disease.
    Musumeci S; D'Agata A; Romano C; Patané R; Cutrona D
    Am J Med Genet; 1988 Feb; 29(2):377-82. PubMed ID: 3354610
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.