BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

184 related articles for article (PubMed ID: 1905498)

  • 1. [Prenatal diagnosis of lysosomal storage disease in the USSR].
    Mirenburg TV; Aronovich EL; Krasnopol'skaia KD; Lebedeva TV; Akhunov VS; Biriukov VB; Bakharev VA; Bartseva OB
    Akush Ginekol (Mosk); 1991 Mar; (3):12-8. PubMed ID: 1905498
    [No Abstract]   [Full Text] [Related]  

  • 2. Diagnosis and prenatal diagnosis of lysosomal storage diseases.
    Shi HP; Guo YF; Zhang WM; Yuan LF; Luo HY; Sun NH; Zhao SM; Zhu MG
    Chin Med J (Engl); 1988 Jun; 101(6):383-7. PubMed ID: 3146466
    [No Abstract]   [Full Text] [Related]  

  • 3. [Experimental and prenatal diagnosis of lysosomal storage diseases].
    Shi HP
    Zhonghua Yi Xue Za Zhi; 1988 Mar; 68(3):124-7, 10. PubMed ID: 3136887
    [No Abstract]   [Full Text] [Related]  

  • 4. Intrafamilial variability in lysosomal storage diseases.
    Zlotogora J
    Am J Med Genet; 1987 Jul; 27(3):633-8. PubMed ID: 3115101
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Prenatal diagnosis of hereditary lysosomal diseases].
    Mirenburg TV; Aronovich EL; Lebedeva TV; Akhunov VS; Krasnopol'skaia KD
    Vopr Med Khim; 1988; 34(4):41-6. PubMed ID: 3143186
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Differential diagnosis and diseases due to enzyme changes.
    Martin-DeLeon PA
    Del Med J; 1979 May; 51(5):267-70, 276-81. PubMed ID: 110628
    [No Abstract]   [Full Text] [Related]  

  • 7. Basic concepts in biochemical antenatal diagnosis.
    Grebner EE
    Obstet Gynecol Clin North Am; 1993 Sep; 20(3):421-31. PubMed ID: 8278142
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Enzyme deficiencies detected on cultured fibroblasts and amniotic cells. Application to prenatal diagnosis].
    Dreyfus JC; Poenaru L
    Ann Biol Clin (Paris); 1975; 33(6):465-72. PubMed ID: 818927
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Selection in favor of lysosomal storage disorders?
    Zlotogora J; Zeigler M; Bach G
    Am J Hum Genet; 1988 Feb; 42(2):271-3. PubMed ID: 3124612
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Intrauterine diagnosis of biochemical disorders.
    Burton BK
    Semin Perinatol; 1980 Jul; 4(3):179-87. PubMed ID: 6932103
    [No Abstract]   [Full Text] [Related]  

  • 11. Evaluation of possible first trimester prenatal diagnosis in lysosomal diseases by trophoblast biopsy.
    Poenaru L; Kaplan L; Dumez J; Dreyfus JC
    Pediatr Res; 1984 Oct; 18(10):1032-4. PubMed ID: 6593685
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Prenatal diagnosis of lysosomal storage diseases].
    Shi HP; Guo YF; Yuan LF; Luo HY; Zhao SM; Sun NH; Zhu MG
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1987 Feb; 9(1):76-8. PubMed ID: 2954695
    [No Abstract]   [Full Text] [Related]  

  • 13. Enzyme studies in GM2 gangliosidiosis, and their application in prenatal diagnosis.
    Kaur M; Verma IC
    Indian J Pediatr; 1995; 62(4):485-9. PubMed ID: 10829910
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Rapid detection of fetal Mendelian disorders: Tay-Sachs disease.
    Guetta E; Peleg L
    Methods Mol Biol; 2008; 444():147-59. PubMed ID: 18425478
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Mucosulfatidosis. Study of 3 familial cases].
    Couchot J; Pluot M; Schmauch MA; Pennaforte F; Fandre M
    Arch Fr Pediatr; 1974 Oct; 31(8):775-95. PubMed ID: 4218948
    [No Abstract]   [Full Text] [Related]  

  • 16. [Cultivation of amniotic fluid cells for the purpose of diagnosing certain metabolic diseases].
    Zolotukhina TV; Tsvetkova IV
    Biull Eksp Biol Med; 1980 Mar; 89(3):344-6. PubMed ID: 7388145
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Detection of trisomy 21 in a fetus during the investigation for Tay-Sachs disease.
    Alpman A; Bora E; Karaca E; Cankaya T; Onay H; Cogulu O; Gunduz C; Kleijer WJ; Ozkinay F
    Genet Couns; 2004; 15(1):99-100. PubMed ID: 15083708
    [No Abstract]   [Full Text] [Related]  

  • 18. Prenatal screening.
    Sillence D; Roy P; Cummins G; West C; Lipson T
    Aust Fam Physician; 1986 Mar; 15(3):318-20. PubMed ID: 3518685
    [No Abstract]   [Full Text] [Related]  

  • 19. [Genetic complementation in the study of mechanisms of inborn errors of metabolism in man (review of the literature)].
    Baskaeva EM
    Vopr Med Khim; 1990; 36(1):13-8. PubMed ID: 2188424
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Enzymatic abnormalities in diseases of sphingolipid metabolism.
    Brady RO
    Clin Chem; 1967 Jul; 13(7):565-77. PubMed ID: 5006481
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 10.