BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

147 related articles for article (PubMed ID: 6303650)

  • 1. Detection of Fabry's disease heterozygotes by enzyme analysis in single fibroblasts after cell sorting.
    Jongkind JF; Verkerk A; Niermeijer MF
    Clin Genet; 1983 Apr; 23(4):261-6. PubMed ID: 6303650
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Fibroblast alpha-galactosidase A activity for identification of Fabry's disease heterozygotes.
    Fensom AH; Benson PF; Grant AR; Jacobs L
    J Inherit Metab Dis; 1980; 2(1):9-12. PubMed ID: 6273649
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Differential assay for lysosomal alpha-galactosidases in human tissues and its application to Fabry's disease.
    Mayes JS; Scheerer JB; Sifers RN; Donaldson ML
    Clin Chim Acta; 1981 May; 112(2):247-51. PubMed ID: 6263521
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Detection of Fabry's disease carriers by enzyme assay of hair roots.
    Hatton CE; Cooper A; Sardharwalla IB
    J Inherit Metab Dis; 1989; 12 Suppl 2():369-71. PubMed ID: 2556612
    [No Abstract]   [Full Text] [Related]  

  • 5. Metabolism of ceramide trihexoside in cultured skin fibroblasts from Fabry's patients, carriers and normal controls.
    Kobayashi T; Shinnoh N; Kuroiwa Y
    J Neurol Sci; 1984 Aug; 65(2):169-77. PubMed ID: 6090593
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular genetic, biochemical, and clinical studies in three families with cardiac Fabry's disease.
    Yoshitama T; Nakao S; Takenaka T; Teraguchi H; Sasaki T; Kodama C; Tanaka A; Kisanuki A; Tei C
    Am J Cardiol; 2001 Jan; 87(1):71-5. PubMed ID: 11137837
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Anderson-Fabry disease: rapid detection of carriers by hair bulb analysis.
    Ejiofor A; Robinson D; Wise D; Hamers M; Tager JM
    J Inherit Metab Dis; 1978; 1(2):71-4. PubMed ID: 229342
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Heterozygote detection in Fabry's disease using mailed hair roots.
    Vermorken AJ; van Bennekom CA; de Bruyn CH; Oei TL; Frohlich J
    Br J Dermatol; 1980 Jul; 103(1):101-3. PubMed ID: 6252938
    [No Abstract]   [Full Text] [Related]  

  • 9. Loss of electron-dense lamellar material from Fabry's disease fibroblasts after enzyme replacement.
    Sifers RN; Mayes JS; Nordquist RE
    Hum Genet; 1983; 65(1):85-7. PubMed ID: 6315565
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical features and genetic analysis of a Chinese kindred with Fabry's disease.
    Tse KC; Chan KW; Tin VP; Yip PS; Tang S; Li FK; Ho YW; Lai KN; Chan TM
    Nephrol Dial Transplant; 2003 Jan; 18(1):182-6. PubMed ID: 12480979
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Fabry's disease presenting with stroke.
    Grewal RP; Barton NW
    Clin Neurol Neurosurg; 1992; 94(2):177-9. PubMed ID: 1324819
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Residual activity of alpha-galactosidase A in Fabry's disease.
    Romeo G; D'Urso M; Pisacane A; Blum E; De Falco A; Ruffilli A
    Biochem Genet; 1975 Oct; 13(9-10):615-28. PubMed ID: 812485
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cultured skin fibroblasts in lipidoses. Enzymatic, histochemical, and ultrastructural relationship in Fabry's Tay-Sachs, and Sandhoff's diseases.
    Yuasa T; Fukuma M; Takashima S; Takaki R
    Arch Pathol Lab Med; 1980 Jun; 104(6):321-7. PubMed ID: 6246846
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Alpha-galactosidase A deficiency--Fabry's disease].
    Tsuji S
    Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):745-8. PubMed ID: 2855953
    [No Abstract]   [Full Text] [Related]  

  • 15. Identification of Fabry's disease by the screening of alpha-galactosidase A activity in male and female hemodialysis patients.
    Tanaka M; Ohashi T; Kobayashi M; Eto Y; Miyamura N; Nishida K; Araki E; Itoh K; Matsushita K; Hara M; Kuwahara K; Nakano T; Yasumoto N; Nonoguchi H; Tomita K
    Clin Nephrol; 2005 Oct; 64(4):281-7. PubMed ID: 16240899
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Endocytotic internalization of alpha-2-macroglobulin: alpha-galactosidase conjugate by cultured fibroblasts derived from Fabry hemizygote.
    Osada T; Kuroda Y; Ikai A
    Biochem Biophys Res Commun; 1987 Jan; 142(1):100-6. PubMed ID: 2434088
    [TBL] [Abstract][Full Text] [Related]  

  • 17. An atypical variant of Fabry's disease in men with left ventricular hypertrophy.
    Nakao S; Takenaka T; Maeda M; Kodama C; Tanaka A; Tahara M; Yoshida A; Kuriyama M; Hayashibe H; Sakuraba H
    N Engl J Med; 1995 Aug; 333(5):288-93. PubMed ID: 7596372
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic inactivation of the alpha-galactosidase locus in carriers of Fabry's disease.
    Romeo G; Migeon BR
    Science; 1970 Oct; 170(3954):180-1. PubMed ID: 5466114
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Fabry's disease: heterozygote detection by hair root analysis.
    Grimm T; Wienker TF; Ropers HH
    Hum Genet; 1976 Jun; 32(3):329-34. PubMed ID: 820627
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A case of Fabry's disease in a patient with no alpha-galactosidase A activity caused by a single amino acid substitution of Pro-40 by Ser.
    Koide T; Ishiura M; Iwai K; Inoue M; Kaneda Y; Okada Y; Uchida T
    FEBS Lett; 1990 Jan; 259(2):353-6. PubMed ID: 2152885
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.