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 *

125 related articles for article (PubMed ID: 2866352)

  • 41. Juvenile and adult metachromatic leukodystrophy: partial restoration of arylsulfatase A (cerebroside sulfatase) activity by inhibitors of thiol proteinases.
    von Figura K; Steckel F; Hasilik A
    Proc Natl Acad Sci U S A; 1983 Oct; 80(19):6066-70. PubMed ID: 6136972
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Molecular basis of different forms of metachromatic leukodystrophy.
    Polten A; Fluharty AL; Fluharty CB; Kappler J; von Figura K; Gieselmann V
    N Engl J Med; 1991 Jan; 324(1):18-22. PubMed ID: 1670590
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Biochemical aspects of globoid and metachromatic leukodystrophies.
    Farooqui AA; Horrocks LA
    Neurochem Pathol; 1984; 2(3):189-218. PubMed ID: 6152665
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Molecular genetics of metachromatic leukodystrophy.
    Gieselmann V; Polten A; Kreysing J; Kappler J; Fluharty A; von Figura K
    Dev Neurosci; 1991; 13(4-5):222-7. PubMed ID: 1687778
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Metachromatic leukodystrophy: a nonsense mutation (Q486X) in the arylsulphatase A (ARSA) gene.
    Harvey JS; Carey WF; Nelson PV; Morris CP
    Hum Mol Genet; 1994 Jan; 3(1):207. PubMed ID: 7909249
    [No Abstract]   [Full Text] [Related]  

  • 46. 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]  

  • 47. Arylsulfatase A in pseudodeficiency.
    Herz B; Bach G
    Hum Genet; 1984; 66(2-3):147-50. PubMed ID: 6143719
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Monozygotic twins with presumed metachromatic leukodystrophy. Activity of arylsulfatase A in serum of patients and family.
    Hashimoto T; Minato H; Kuroda Y; Toshima K; Ohara K; Miyao M
    Arch Neurol; 1978 Oct; 35(10):689-91. PubMed ID: 29593
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Multiple sulfatase deficiency with a novel biochemical presentation.
    Constantopoulos G
    Eur J Pediatr; 1988 Aug; 147(6):634-8. PubMed ID: 2903054
    [TBL] [Abstract][Full Text] [Related]  

  • 50. [Enzymologic detection of metachromatic leukodystrophy: limitations in prenatal diagnosis].
    Turpin JC
    Sem Hop; 1977 Dec; 53(42):2445-6. PubMed ID: 23583
    [No Abstract]   [Full Text] [Related]  

  • 51. Studies in metachromatic leukodystrophy. XIII. Purification of sulfatase A from normal human liver.
    Collins J; Yamada W; Worth W; Austin J
    Adv Exp Med Biol; 1976; 68():225-32. PubMed ID: 7103
    [No Abstract]   [Full Text] [Related]  

  • 52. Prevalence of partial cerebroside sulfate sulfatase (arylsulfatase A) defect in adult psychiatric patients.
    Shah SN; Johnson RC; Stone RK; Mahon-Haft H
    Biol Psychiatry; 1985 Jan; 20(1):50-7. PubMed ID: 2856894
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Lysosomal leukodystrophies: Krabbe disease and metachromatic leukodystrophy.
    Kohlschütter A
    Handb Clin Neurol; 2013; 113():1611-8. PubMed ID: 23622382
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Immunological evidence for deficiency in an activator protein for sulfatide sulfatase in a variant form of metachromatic leukodystrophy.
    Inui K; Emmett M; Wenger DA
    Proc Natl Acad Sci U S A; 1983 May; 80(10):3074-7. PubMed ID: 6134282
    [TBL] [Abstract][Full Text] [Related]  

  • 55. An arylsulfatase A (ARSA) missense mutation (T274M) causing late-infantile metachromatic leukodystrophy.
    Harvey JS; Nelson PV; Carey WF; Robertson EF; Morris CP
    Hum Mutat; 1993; 2(4):261-7. PubMed ID: 8104633
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Multiple deficiency of mucopolysaccharide sulfatases in mucosulfatidosis.
    Basner R; von Figura K; Glössl J; Klein U; Kresse H; Mlekusch W
    Pediatr Res; 1979 Dec; 13(12):1316-8. PubMed ID: 523191
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Prevalence of arylsulfatase A pseudodeficiency allele in metachromatic leukodystrophy patients from Poland.
    Lugowska A; Czartoryska B; Tylki-Szymańska A; Bisko M; Zimowski JG; Berger J; Molzer B
    Eur Neurol; 2000; 44(2):104-7. PubMed ID: 10965162
    [TBL] [Abstract][Full Text] [Related]  

  • 58. [Analysis of phenotype and genotype in a family with late infantile metachromatic leukodystrophy].
    Yang J; Cao J; Li Y; Zheng H; Li J; Liang Y; Liu Z; Wang L; Zhang C
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Oct; 31(5):615-8. PubMed ID: 25297594
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Juvenile-onset metachromatic leukodystrophy: biochemical and electrophysiologic studies.
    Clark JR; Miller RG; Vidgoff JM
    Neurology; 1979 Mar; 29(3):346-3. PubMed ID: 36575
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Searching for mutations in the arylsulphatase A gene.
    Salamon MB; Christensen E; Schwartz M
    J Inherit Metab Dis; 1994; 17(3):311-4. PubMed ID: 7807940
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.