171 related articles for article (PubMed ID: 26577183)
1. 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]
2. 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]
3. Disease-causing mutations in cis with the common arylsulfatase A pseudodeficiency allele compound the difficulties in accurately identifying patients and carriers of metachromatic leukodystrophy.
Rafi MA; Coppola S; Liu SL; Rao HZ; Wenger DA
Mol Genet Metab; 2003 Jun; 79(2):83-90. PubMed ID: 12809637
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. 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]
7. Arylsulfatase A pseudodeficiency: a common polymorphism which is associated with a unique haplotype.
Zlotogora J; Furman-Shaharabani Y; Goldenfum S; Winchester B; von Figura K; Gieselmann V
Am J Med Genet; 1994 Aug; 52(2):146-50. PubMed ID: 7801999
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Arylsulfatase A pseudodeficiency--incidence in Poland.
Czartoryska B; Zimowski JG; Bisko M; Górska D
Eur J Hum Genet; 1996; 4(5):301-3. PubMed ID: 8946177
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Two new polymorphisms in the arylsulfatase A gene and their haplotype associations with normal, metachromatic leukodystrophy and pseudodeficiency alleles.
Coulter-Mackie M; Gagnier L
Am J Med Genet; 1997 Nov; 73(1):32-5. PubMed ID: 9375919
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Evolutionary origins of two tightly linked mutations in arylsulfatase-A pseudodeficiency.
Ott R; Waye JS; Chang PL
Hum Genet; 1997 Dec; 101(2):135-40. PubMed ID: 9402957
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Arylsulfatase A in pseudodeficiency.
Herz B; Bach G
Hum Genet; 1984; 66(2-3):147-50. PubMed ID: 6143719
[TBL] [Abstract][Full Text] [Related]
17. Identification of 12 novel mutations and two new polymorphisms in the arylsulfatase A gene: haplotype and genotype-phenotype correlation studies in Spanish metachromatic leukodystrophy patients.
Gort L; Coll MJ; Chabás A
Hum Mutat; 1999; 14(3):240-8. PubMed ID: 10477432
[TBL] [Abstract][Full Text] [Related]
18. Determination of frequencies of alleles, associated with the pseudodeficiency of lysosomal hydrolases, in population of Ukraine.
Olkhovych NV; Gorovenko NG
Ukr Biochem J; 2016; 88(5):96-106. PubMed ID: 29235819
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. A genome wide SNP genotyping study in the Tunisian population: specific reporting on a subset of common breast cancer risk loci.
Hamdi Y; Ben Rekaya M; Jingxuan S; Nagara M; Messaoud O; Benammar Elgaaied A; Mrad R; Chouchane L; Boubaker MS; Abdelhak S; Boussen H; Romdhane L
BMC Cancer; 2018 Dec; 18(1):1295. PubMed ID: 30594178
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
