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 *

93 related articles for article (PubMed ID: 1687779)

  • 1. Phenotypic consequences of low arylsulfatase A genotypes (ASAp/ASAp and ASA-/ASAp): does there exist an association with multiple sclerosis?
    Kappler J; Pötter W; Gieselmann V; Kiessling W; Friedl W; Propping P
    Dev Neurosci; 1991; 13(4-5):228-31. PubMed ID: 1687779
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Arylsulfatase a gene polymorphisms in relapsing remitting multiple sclerosis: genotype-phenotype correlation and estimation of disease progression.
    Baronica KB; Mlinac K; Ozretić D; Vladić A; Bognar SK
    Coll Antropol; 2011 Jan; 35 Suppl 1():11-6. PubMed ID: 21648305
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Pseudodeficiency of arylsulfatase A: a common genetic polymorphism with possible disease implications.
    Hohenschutz C; Eich P; Friedl W; Waheed A; Conzelmann E; Propping P
    Hum Genet; 1989 Apr; 82(1):45-8. PubMed ID: 2565866
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genotype-phenotype relationship in various degrees of arylsulfatase A deficiency.
    Kappler J; Leinekugel P; Conzelmann E; Kleijer WJ; Kohlschütter A; Tønnesen T; Rochel M; Freycon F; Propping P
    Hum Genet; 1991 Mar; 86(5):463-70. PubMed ID: 1673113
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutations in the arylsulfatase A pseudodeficiency allele causing metachromatic leukodystrophy.
    Gieselmann V; Fluharty AL; Tønnesen T; Von Figura K
    Am J Hum Genet; 1991 Aug; 49(2):407-13. PubMed ID: 1678251
    [TBL] [Abstract][Full Text] [Related]  

  • 6. An assay for the rapid detection of the arylsulfatase A pseudodeficiency allele facilitates diagnosis and genetic counseling for metachromatic leukodystrophy.
    Gieselmann V
    Hum Genet; 1991 Jan; 86(3):251-5. PubMed ID: 1671769
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Arylsulfatase A pseudodeficiency incidence in Turkey.
    Emre S; Topçu M; Terzioğlu M; Renda Y
    Turk J Pediatr; 2000; 42(2):115-7. PubMed ID: 10936976
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Arylsulfatase A pseudodeficiency in healthy Brazilian individuals.
    Pedron CG; Gaspar PA; Giugliani R; Pereira ML
    Braz J Med Biol Res; 1999 Aug; 32(8):941-5. PubMed ID: 10454754
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Diffuse-disseminated sclerosis combined with partial arylsulfatase A (ASA) deficiency. Mixed heterozygosity of ASA- and pseudo-ASA-deficiency?
    Peiffer J; Harzer K; Schlote W
    Neuropediatrics; 1984 May; 15(2):59-62. PubMed ID: 6146104
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Probable metachromatic leukodystrophy/pseudodeficiency compound heterozygote at the arylsulfatase A locus with neurological and psychiatric symptomatology.
    Hohenschutz C; Friedl W; Schlör KH; Waheed A; Conzelmann E; Sandhoff K; Propping P
    Am J Med Genet; 1988 Sep; 31(1):169-75. PubMed ID: 2906225
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Croatian population data for arylsulfatase a pseudodeficiency-associated mutations in healthy subjects, and in patients with Alzheimer-type dementia and Down syndrome.
    Bognar SK; Furac I; Kubat M; Cosović C; Demarin V
    Arch Med Res; 2002; 33(5):473-7. PubMed ID: 12459318
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Arylsulfatase A pseudodeficiency: loss of a polyadenylylation signal and N-glycosylation site.
    Gieselmann V; Polten A; Kreysing J; von Figura K
    Proc Natl Acad Sci U S A; 1989 Dec; 86(23):9436-40. PubMed ID: 2574462
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A method for rapid detection of arylsulfatase A pseudodeficiency mutations.
    Ricketts MH; Zhang X; Manowitz P
    Hum Hered; 1995; 45(4):235-40. PubMed ID: 7558057
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Arylsulfatase A pseudodeficiency in Mexico: Enzymatic activity and haplotype analysis.
    Juárez-Osuna JA; Mendoza-Ruvalcaba SC; Porras-Dorantes A; Da Silva-José TD; García-Ortiz JE
    Mol Genet Genomic Med; 2020 Aug; 8(8):e1305. PubMed ID: 32431092
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Pseudodeficiency of arylsulphatase A: strategy for clarification of genotype in families of subjects with low ASA activity and neurological symptoms.
    Leistner S; Young E; Meaney C; Winchester B
    J Inherit Metab Dis; 1995; 18(6):710-6. PubMed ID: 8750609
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Metachromatic leukodystrophy: multiple nonfunctional and pseudodeficiency alleles in a pedigree: problems with diagnosis and counseling.
    Francis GS; Bonni A; Shen N; Hechtman P; Yamut B; Carpenter S; Karpati G; Chang PL
    Ann Neurol; 1993 Aug; 34(2):212-8. PubMed ID: 8101704
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Frequency of arylsulphatase A pseudodeficiency associated mutations in a healthy population.
    Barth ML; Ward C; Harris A; Saad A; Fensom A
    J Med Genet; 1994 Sep; 31(9):667-71. PubMed ID: 7815433
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Determination of arylsulfatase A pseudodeficiency allele and haplotype frequency in the Tunisian population.
    Ben Halim N; Dorboz I; Kefi R; Kharrat N; Eymard-Pierre E; Nagara M; Romdhane L; Ben Alaya-Bouafif N; Rebai A; Miladi N; Boespflug-Tanguy O; Abdelhak S
    Neurol Sci; 2016 Mar; 37(3):403-9. PubMed ID: 26577183
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.