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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

157 related items for PubMed ID: 26223439

  • 1. Inherited metabolic disorders: prenatal diagnosis of lysosomal storage disorders.
    Verma J, Thomas DC, Sharma S, Jhingan G, Saxena R, Kohli S, Puri RD, Bijarnia S, Verma IC.
    Prenat Diagn; 2015 Nov; 35(11):1137-47. PubMed ID: 26223439
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. Early prenatal diagnosis of lysosomal storage disorders by enzymatic and molecular analysis.
    Li D, Lin Y, Huang Y, Zhang W, Jiang M, Li X, Zhao X, Sheng H, Yin X, Su X, Shao Y, Liu Z, Li D, Li F, Liao C, Liu L.
    Prenat Diagn; 2018 Sep; 38(10):779-787. PubMed ID: 29966168
    [Abstract] [Full Text] [Related]

  • 4. [Prenatal diagnosis of lysosomal enzymopathies in the Czech Republic].
    Poupetová H, Ledvinová J, Chudoba D, Hrebícek M, Kozich V, Macek M, Elleder M.
    Cas Lek Cesk; 2000 Aug 02; 139(15):468-74. PubMed ID: 22666927
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. Electron microscopy of chorionic villus samples for prenatal diagnosis of lysosomal storage disorders.
    Fowler DJ, Anderson G, Vellodi A, Malone M, Sebire NJ.
    Ultrastruct Pathol; 2007 Aug 02; 31(1):15-21. PubMed ID: 17455094
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. First-trimester biochemical and molecular diagnoses using chorionic villi: high accuracy in the U.S. collaborative study.
    Desnick RJ, Schuette JL, Golbus MS, Jackson L, Lubs HA, Ledbetter DH, Mahoney MJ, Pergament E, Simpson JL, Zachary JM.
    Prenat Diagn; 1992 May 02; 12(5):357-72. PubMed ID: 1523203
    [Abstract] [Full Text] [Related]

  • 11. Prenatal diagnosis of heterozygosis in a pregnancy at risk for Wolman's disease at the 8th week of gestation.
    Bona G, Gallina MR, Dolfin G, Iavarone A, Perona A, Zaffaroni M.
    Panminerva Med; 1989 May 02; 31(4):180-2. PubMed ID: 2633108
    [Abstract] [Full Text] [Related]

  • 12. Prenatal enzymatic diagnosis of Krabbe disease (globoid-cell leukodystrophy) using chorionic villi. Pitfalls in the use of uncultured villi.
    Harzer K, Schuster I.
    Hum Genet; 1989 Dec 02; 84(1):83-5. PubMed ID: 2606482
    [Abstract] [Full Text] [Related]

  • 13. First-trimester prenatal diagnosis performed on pregnant women with fetal ultrasound abnormalities: the reliability of interphase fluorescence in situ hybridization (FISH) on mesenchymal core for the main aneuploidies.
    Toutain J, Epiney M, Begorre M, Dessuant H, Vandenbossche F, Horovitz J, Saura R.
    Eur J Obstet Gynecol Reprod Biol; 2010 Apr 02; 149(2):143-6. PubMed ID: 20045588
    [Abstract] [Full Text] [Related]

  • 14. Comparative study of 15 lysosomal enzymes in chorionic villi and cultured amniotic fluid cells. Early prenatal diagnosis in seven pregnancies at risk for lysosomal storage diseases.
    Gatti R, Lombardo C, Filocamo M, Borrone C, Porro E.
    Prenat Diagn; 1985 Apr 02; 5(5):329-36. PubMed ID: 3934658
    [Abstract] [Full Text] [Related]

  • 15. The arylsulphatases of chorionic villi: potential problems in the first-trimester diagnosis of metachromatic leucodystrophy and Maroteaux-Lamy disease.
    Sanguinetti N, Marsh J, Jackson M, Fensom AH, Warren RC, Rodeck CH.
    Clin Genet; 1986 Oct 02; 30(4):302-8. PubMed ID: 3098467
    [Abstract] [Full Text] [Related]

  • 16. Lysosomal storage diseases presenting as transient or persistent hydrops fetalis.
    Bonduelle M, Lissens W, Goossens A, De Catte L, Foulon W, Denis R, Jauniaux E, Liebaers I.
    Genet Couns; 1991 Oct 02; 2(4):227-32. PubMed ID: 1799421
    [Abstract] [Full Text] [Related]

  • 17. Rapid detection of fetal Mendelian disorders: Tay-Sachs disease.
    Guetta E, Peleg L.
    Methods Mol Biol; 2008 Oct 02; 444():147-59. PubMed ID: 18425478
    [Abstract] [Full Text] [Related]

  • 18. Aryl sulphatase isoenzymes of chorionic villi: implications for prenatal diagnosis.
    Giles L, Cooper A, Fowler B, Sardharwalla IB, Donnai P.
    Prenat Diagn; 1987 May 02; 7(4):245-52. PubMed ID: 2884655
    [Abstract] [Full Text] [Related]

  • 19. Utility of amniotic fluid chitotriosidase in the prenatal diagnosis of lysosomal storage disorders.
    Kadali S, Madalasa T, Reddy GM, Naushad SM.
    Clin Biochem; 2018 Nov 02; 61():40-44. PubMed ID: 30205089
    [Abstract] [Full Text] [Related]

  • 20. Prenatal diagnosis of lysosomal storage diseases.
    Lake BD, Young EP, Winchester BG.
    Brain Pathol; 1998 Jan 02; 8(1):133-49. PubMed ID: 9458172
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.