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 *

120 related articles for article (PubMed ID: 3146334)

  • 1. Placental pathology and prenatal diagnosis of infantile type of neuronal ceroid-lipofuscinosis.
    Rapola J; Santavuori P; Heiskala H
    Am J Med Genet Suppl; 1988; 5():99-103. PubMed ID: 3146334
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prenatal diagnosis of the infantile type of neuronal ceroid lipofuscinosis by electron microscopic investigation of human chorionic villi.
    Rapola J; Salonen R; Ammälä P; Santavuori P
    Prenat Diagn; 1990 Sep; 10(9):553-9. PubMed ID: 2176289
    [TBL] [Abstract][Full Text] [Related]  

  • 3. First-trimester diagnosis of juvenile neuronal ceroid lipofuscinosis by demonstration of fingerprint inclusions in chorionic villi.
    Conradi NG; Uvebrant P; Hökegård KH; Wahlström J; Mellqvist L
    Prenat Diagn; 1989 Apr; 9(4):283-7. PubMed ID: 2541423
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Ultrastructural studies as a method of prenatal diagnosis of neuronal ceroid-lipofuscinosis.
    MacLeod PM; Nag S; Berry C
    Am J Med Genet Suppl; 1988; 5():93-7. PubMed ID: 3146333
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prenatal diagnosis of infantile neuronal ceroid-lipofuscinosis, INCL: morphological aspects.
    Rapola J; Salonen R; Ammälä P; Santavuori P
    J Inherit Metab Dis; 1993; 16(2):349-52. PubMed ID: 8411996
    [No Abstract]   [Full Text] [Related]  

  • 6. Prenatal diagnosis of variant late infantile neuronal ceroid lipofuscinosis (vLINCL[Finnish]; CLN5).
    Rapola J; Lähdetie J; Isosomppi J; Helminen P; Penttinen M; Järvelä I
    Prenat Diagn; 1999 Jul; 19(7):685-8. PubMed ID: 10419622
    [TBL] [Abstract][Full Text] [Related]  

  • 7. DNA-based prenatal diagnosis of the infantile form of neuronal ceroid lipofuscinosis (INCL, CLN1).
    Järvelä I; Rapola J; Peltonen L; Puhakka L; Vesa J; Ammälä P; Salonen R; Ryynänen M; Haring P; Mustonen A
    Prenat Diagn; 1991 May; 11(5):323-8. PubMed ID: 1680233
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Lymphocyte inclusions in Finnish-variant late infantile neuronal ceroid lipofuscinosis (CLN5).
    Rapola J; Lake BD
    Neuropediatrics; 2000 Feb; 31(1):33-4. PubMed ID: 10774993
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal diagnosis of infantile neuronal ceroid-lipofuscinosis: a combined electron microscopic and molecular genetic approach.
    Goebel HH; Vesa J; Reitter B; Goecke TO; Schneider-Rätzke B; Merz E
    Brain Dev; 1995; 17(2):83-8. PubMed ID: 7625554
    [TBL] [Abstract][Full Text] [Related]  

  • 10. First-trimester diagnosis of infantile neuronal ceroid lipofuscinosis (INCL) using PPT enzyme assay and CLN1 mutation analysis.
    de Vries BB; Kleijer WJ; Keulemans JL; Voznyi YV; Franken PF; Eurlings MC; Galjaard RJ; Losekoot M; Catsman-Berrevoets CE; Breuning MH; Taschner PE; van Diggelen OP
    Prenat Diagn; 1999 Jun; 19(6):559-62. PubMed ID: 10416973
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Successful DNA-based prenatal exclusion of juvenile neuronal ceroid lipofuscinosis.
    Uvebrant P; Björck E; Conradi N; Hökegård KH; Martinsson T; Wahlström J
    Prenat Diagn; 1993 Jul; 13(7):651-7. PubMed ID: 8105459
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal ultrastructural diagnosis in the neuronal ceroid-lipofuscinoses.
    Goebel HH
    Pathol Res Pract; 1994 Aug; 190(7):728-33. PubMed ID: 7808971
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A new simple enzyme assay for pre- and postnatal diagnosis of infantile neuronal ceroid lipofuscinosis (INCL) and its variants.
    Voznyi YV; Keulemans JL; Mancini GM; Catsman-Berrevoets CE; Young E; Winchester B; Kleijer WJ; van Diggelen OP
    J Med Genet; 1999 Jun; 36(6):471-4. PubMed ID: 10874636
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prenatal diagnosis of neuronal ceroid-lipofuscinoses.
    MacLeod PM; Dolman CL; Nickel RE; Chang E; Nag S; Zonana J; Silvey K
    Am J Med Genet; 1985 Dec; 22(4):781-9. PubMed ID: 4073127
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Profound infantile neuroretinal dysfunction in a heterozygote for the CLN3 genetic defect.
    de los Reyes E; Dyken PR; Phillips P; Brodsky M; Bates S; Glasier C; Mrak RE
    J Child Neurol; 2004 Jan; 19(1):42-6. PubMed ID: 15032383
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Morphological approaches to the prenatal diagnosis of late-infantile and juvenile Batten disease.
    Lake BD
    J Inherit Metab Dis; 1993; 16(2):345-8. PubMed ID: 8411995
    [No Abstract]   [Full Text] [Related]  

  • 17. First-trimester diagnosis of late-infantile neuronal ceroid lipofuscinosis (LINCL) by tripeptidyl peptidase I assay and CLN2 mutation analysis.
    Kleijer WJ; van Diggelen OP; Keulemans JL; Losekoot M; Garritsen VH; Stroink H; Majoor-Krakauer D; Franken PF; Eurlings MC; Taschner PE; Los FJ; Galjaard RJ
    Prenat Diagn; 2001 Feb; 21(2):99-101. PubMed ID: 11241534
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Exclusion of late infantile neuronal ceroid lipofuscinosis (LINCL) in a fetus by assay of tripeptidyl peptidase I in chorionic villi.
    Young EP; Winchester BG; Peter Logan W; Wheeler RB; Lake BD
    Prenat Diagn; 2000 Apr; 20(4):337-9. PubMed ID: 10740208
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Suction biopsy of rectal mucosa in the diagnosis of infantile and juvenile types of neuronal ceroid lipofuscinoses.
    Rapola J; Santavuori P; Savilahti E
    Hum Pathol; 1984 Apr; 15(4):352-60. PubMed ID: 6714966
    [TBL] [Abstract][Full Text] [Related]  

  • 20. DNA diagnosis and identification of carriers of infantile and juvenile neuronal ceroid lipofuscinoses.
    Syvänen AC; Järvelä I; Paunio T; Vesa J
    Neuropediatrics; 1997 Feb; 28(1):63-6. PubMed ID: 9151326
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.