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 *

154 related articles for article (PubMed ID: 4895581)

  • 1. The use of white cells as a source of diagnostic material for lipid storage diseases.
    Snyder RA; Brady RO
    Clin Chim Acta; 1969 Aug; 25(2):331-8. PubMed ID: 4895581
    [No Abstract]   [Full Text] [Related]  

  • 2. The adnormal biochemistry of inherited disorders of lipid metabolism.
    Brady RO
    Fed Proc; 1973 Jun; 32(6):1660-7. PubMed ID: 4351098
    [No Abstract]   [Full Text] [Related]  

  • 3. Metachromatic leukodystrophy: diagnosis with samples of venous blood.
    Percy AK; Brady RO
    Science; 1968 Aug; 161(3841):594-5. PubMed ID: 5668537
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Outlooks offered by lysosomal enzyme determination in neuropediatrics].
    Turpin JC; Dubois G; Moréno P; Baumann N
    Arch Fr Pediatr; 1972; 29(6):674. PubMed ID: 5078373
    [No Abstract]   [Full Text] [Related]  

  • 5. Diagnosis of gaucher's disease and niemann-pick disease with small samples of venous blood.
    Kampine JP; Brady RO; Kanfer JN; Feld M; Shapiro D
    Science; 1967 Jan; 155(3758):86-8. PubMed ID: 6015567
    [TBL] [Abstract][Full Text] [Related]  

  • 6. An improved method for the determination of leukocyte arylsulfatase A and its application to the diagnosis of metachromatic leukodystrophy in homozygous and heterozygous states.
    Potter JL; Timmons GD; Rinehart L; Witmer EJ
    Clin Chim Acta; 1972 Jul; 39(2):518-23. PubMed ID: 5043787
    [No Abstract]   [Full Text] [Related]  

  • 7. [Diagnostic value of the determination of intraleukocytic arylsulfatase for the early detection of metachromatic leukodystrophy].
    Baumann N; Turpin JC; Castaigne P
    Presse Med (1893); 1971 Jan; 79(6):244-5. PubMed ID: 5546796
    [No Abstract]   [Full Text] [Related]  

  • 8. Chemical detection of metachromatic leukodystrophy in disease and carrier states.
    Hackett TN; Hackett RJ; Bray PF; Madsen JA
    Am J Dis Child; 1971 Sep; 122(3):223-5. PubMed ID: 5568583
    [No Abstract]   [Full Text] [Related]  

  • 9. Deficiency of glucosylsphingosine: beta-glucosidase in Gaucher disease.
    Raghavan SS; Mumford RA; Kanfer JN
    Biochem Biophys Res Commun; 1973 Sep; 54(1):256-63. PubMed ID: 4741565
    [No Abstract]   [Full Text] [Related]  

  • 10. [Congenital lysosomal diseases].
    Romanowska-Gõrecka B
    Pol Arch Med Wewn; 1972 Apr; 48(4):425-9. PubMed ID: 4556749
    [No Abstract]   [Full Text] [Related]  

  • 11. Cerebral lipidoses.
    Brady RO
    Annu Rev Med; 1970; 21():317-34. PubMed ID: 4915725
    [No Abstract]   [Full Text] [Related]  

  • 12. Late adult metachromatic leukodystrophy. Arylsulfatase A activity of leukocytes in two families.
    Pilz H
    Arch Neurol; 1972 Jul; 27(1):87-90. PubMed ID: 5049684
    [No Abstract]   [Full Text] [Related]  

  • 13. Enzyme replacement in Fabry's disease, an inborn error of metabolism.
    Mapes CA; Anderson RL; Sweeley CC; Desnick RJ; Krivit W
    Science; 1970 Sep; 169(3949):987-9. PubMed ID: 4914726
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Infantile and adult-onset metachromatic leukodystrophy. Biochemical comparisons and predictive diagnosis.
    Percy AK; Kaback MM
    N Engl J Med; 1971 Sep; 285(14):785-7. PubMed ID: 5567265
    [No Abstract]   [Full Text] [Related]  

  • 15. 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]  

  • 16. Prenatal diagnosis of lipid storage diseases.
    Brady RO
    Clin Chem; 1970 Oct; 16(10):811-5. PubMed ID: 4926373
    [No Abstract]   [Full Text] [Related]  

  • 17. Metachromatic leukodystrophy: ambiguity of heterozygote identification.
    Kihara H; Porter MT; Fluharty AL; Scott ML; De la Flor SD; Trammell JL; Nakamura RN
    Am J Ment Defic; 1973 Jan; 77(4):389-94. PubMed ID: 4706397
    [No Abstract]   [Full Text] [Related]  

  • 18. Studies on cerebral lipidosis. Enzymatic diagnosis of metachromatic leukodystrophy.
    Yabuuchi H; Sumi K
    Acta Paediatr Jpn; 1970 Dec; 12(2):1-3. PubMed ID: 4993715
    [No Abstract]   [Full Text] [Related]  

  • 19. Studies on arylsulfatase-A activity in metachromatic leucodystrophy.
    Komiya K; Arima M
    Paediatr Univ Tokyo; 1970 Dec; 18():99-104. PubMed ID: 5535257
    [No Abstract]   [Full Text] [Related]  

  • 20. Arylsulfatase A activity in human urine: quantitative studies on patients with lysosomal disorders including metachromatic leukodystrophy.
    Thomas GH; Howell RR
    Clin Chim Acta; 1972 Jan; 36(1):99-103. PubMed ID: 5007723
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.