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 *

127 related articles for article (PubMed ID: 6114638)

  • 1. Retinal pigment epithelial degeneration and arylsulfatase A deficiency.
    Zlotogora J; Schaap T; Bach G
    Am J Ophthalmol; 1981 Jul; 92(1):136-8. PubMed ID: 6114638
    [No Abstract]   [Full Text] [Related]  

  • 2. Retinal pigment epithelial degeneration associated with leukocytic arylsulfatase A deficiency.
    Weiter JJ; Feingold M; Kolodny EH; Raghaven SS
    Am J Ophthalmol; 1980 Dec; 90(6):768-72. PubMed ID: 6108718
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Very low arylsulfatase A and cerebroside sulfatase activities in leukocytes of healthy members of metachromatic leukodystrophy family.
    Dubois G; Harzer K; Baumann N
    Am J Hum Genet; 1977 Mar; 29(2):191-4. PubMed ID: 15452
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genotype assignments in a family with the pseudo arylsulfatase a deficiency trait without metachromatic leukodystrophy.
    Kihara H; Meek WE; Fluharty AL
    Pediatr Res; 1984 Oct; 18(10):1021-2. PubMed ID: 6149514
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Complementation of arylsulfatase A in somatic hybrids of metachromatic leukodystrophy and multiple sulfatase deficiency disorder fibroblasts.
    Chang PL; Davidson RG
    Proc Natl Acad Sci U S A; 1980 Oct; 77(10):6166-70. PubMed ID: 6108562
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Impaired cerebroside sulfate hydrolysis in fibroblasts of sibs with "pseudo" arylsulfatase A deficiency without metachromatic leukodystrophy.
    Hreidarsson SJ; Thomas GH; Kihara H; Fluharty AL; Kolodny EH; Moser HW; Reynolds LW
    Pediatr Res; 1983 Sep; 17(9):701-4. PubMed ID: 6137805
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Diagnosis of pseudo-arylsulfatase A deficiency with electrophoretic techniques.
    Chang PL; Rosa NE; Varey PA; Kihara H; Kolodny EH; Davidson RG
    Pediatr Res; 1984 Oct; 18(10):1042-5. PubMed ID: 6149515
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic heterogeneity in metachromatic leukodystrophy.
    Kihara H
    Am J Hum Genet; 1982 Mar; 34(2):171-81. PubMed ID: 6122378
    [No Abstract]   [Full Text] [Related]  

  • 9. Metachromatic leukodystrophy caused by a partial cerebroside sulfatase.
    Kihara H; Fluharty AL; O'Brien JS; Fish CH
    Clin Genet; 1982 Apr; 21(4):253-61. PubMed ID: 6125284
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic complementation in somatic cell hybrids of cerebroside sulfatase activator deficiency and metachromatic leukodystrophy fibroblasts.
    Kihara H; Tsay KK; Fluharty AL
    Hum Genet; 1984; 66(4):300-1. PubMed ID: 6144627
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Pseudodeficiencies in lysosomal storage disorders.
    Zlotogora J; Bach G
    Lancet; 1985 Dec; 2(8467):1296. PubMed ID: 2866352
    [No Abstract]   [Full Text] [Related]  

  • 12. Multiple sulfatase deficiency.
    Soong BW; Casamassima AC; Fink JK; Constantopoulos G; Horwitz AL
    Neurology; 1988 Aug; 38(8):1273-5. PubMed ID: 2899861
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Problems in the clinical interpretation of arylsulfatase A deficiency.
    Zlotogora J; Schaap T; Bach G
    Am J Med Genet; 1981; 10(4):413-5. PubMed ID: 6120651
    [No Abstract]   [Full Text] [Related]  

  • 14. Discussion: Metachromatic leukodystrophy, an unusual case with a subtle cerebroside sulfatase defect.
    Kihara H
    UCLA Forum Med Sci; 1975; (18):501-6. PubMed ID: 828
    [No Abstract]   [Full Text] [Related]  

  • 15. A variant form of metachromatic leukodystrophy without arylsulfatase deficiency.
    Hahn AF; Gordon BA; Hinton GG; Gilbert JJ
    Ann Neurol; 1982 Jul; 12(1):33-6. PubMed ID: 6126151
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Metachromatic leukodystrophy].
    Aracena M; Valenzuela E; Selman E; Milos C
    Rev Chil Pediatr; 1984; 55(6):411-3. PubMed ID: 6152638
    [No Abstract]   [Full Text] [Related]  

  • 17. Metachromatic leukodystrophy and pseudoarylsulfatase A deficiency in a Danish family.
    Tønnesen T; Bro PV; Brøndum Nielsen K; Lykkelund C
    Acta Paediatr Scand; 1983 Mar; 72(2):175-8. PubMed ID: 6132516
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Arylsulfatase deficiency and various metabolic diseases].
    Czyzewska K; Działoszyński L
    Pediatr Pol; 1978 Sep; 53(9):1129-35. PubMed ID: 30935
    [No Abstract]   [Full Text] [Related]  

  • 19. Prenatal diagnosis of metachromatic leukodystrophy in a family with pseudo arylsulfatase A deficiency by the cerebroside sulfate loading test.
    Kihara H; Ho CK; Fluharty AL; Tsay KK; Hartlage PL
    Pediatr Res; 1980 Mar; 14(3):224-7. PubMed ID: 6104322
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Arylsulfatase A deficiency-metachromatic leukodystrophy].
    Eto Y
    Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):749-52. PubMed ID: 2908400
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.