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 *

145 related articles for article (PubMed ID: 6315565)

  • 21. Fabry's disease with partially deficient hydrolysis of ceramide trihexoside.
    Kobayashi T; Kira J; Shinnoh N; Goto I; Kuroiwa Y
    J Neurol Sci; 1985 Feb; 67(2):179-85. PubMed ID: 2984338
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Fabry's disease: biochemical and histochemical studies on hair roots for carrier detection.
    Vermorken AJ; Weterings PJ; Spierenburg GT; vanBennekom CA; Wirtz P; deBruyn CH; Oei TL
    Br J Dermatol; 1978 Feb; 98(2):191-6. PubMed ID: 204324
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Silicon nephropathy mimicking Fabry's disease.
    Banks DE; Milutinovic J; Desnick RJ; Grabowski GA; Lapp NL; Boehlecke BA
    Am J Nephrol; 1983; 3(5):279-84. PubMed ID: 6416069
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. A microtechnique for quantitative measurements of acid hydrolases in fibroblasts. Its application in diagnosis of Fabry disease and enzyme replacement studies.
    Hasholt L; Sørensen SA
    Clin Chim Acta; 1984 Sep; 142(2):257-61. PubMed ID: 6094040
    [No Abstract]   [Full Text] [Related]  

  • 26. Cardiopulmonary involvement in Fabry's disease.
    Koskenvuo JW; Kantola IM; Nuutila P; Knuuti J; Parkkola R; Mononen I; Hurme S; Kalliokoski R; Viikari JS; Wendelin-Saarenhovi M; Kiviniemi TO; Hartiala JJ
    Acta Cardiol; 2010 Apr; 65(2):185-92. PubMed ID: 20458826
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Cytoplasmic inclusions of Fabry's disease. Ultrastructural demonstration of their presence in urine sediment.
    Tubbs RR; Gephardt GN; McMahon JT; Hall PM; Gifford RW
    Arch Pathol Lab Med; 1981 Jul; 105(7):361-2. PubMed ID: 6264885
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Detection of Fabry's disease heterozygotes by hair root analysis.
    Beaudet AL; Caskey CT
    Clin Genet; 1978 Mar; 13(3):251-8. PubMed ID: 205381
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Substrate specificity of multiple forms of human alpha-D-galactosidase and alpha-D-fucosidase].
    Baskaeva EM; Shono NI; Kozlova IK; Vidershaĭn GIa
    Biokhimiia; 1989 Mar; 54(3):421-6. PubMed ID: 2546612
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. ConA-mediated binding and uptake of purified alpha-galactosidase A in Fabry fibroblasts.
    Hasholt L; Sørensen SA
    Exp Cell Res; 1983 Oct; 148(2):405-11. PubMed ID: 6313412
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Neurological presentation of Fabry's disease in a 52 year old man.
    Mohanraj R; Leach JP; Broome JC; Smith DF
    J Neurol Neurosurg Psychiatry; 2002 Sep; 73(3):340-2. PubMed ID: 12185177
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Angiokeratoma corporis diffusum (Fabry's disease). Update. Apropos of 2 cases].
    Larralde de Luna M; García Díaz R; Sánchez G; Ilari R; Pierini AM; Campoy C; Chamoles NH
    Med Cutan Ibero Lat Am; 1985; 13(2):129-40. PubMed ID: 2995736
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Uptake of lysosomal enzymes by human fibroblasts: lack of uptake of fungal or plant glycosidases in comparison with a mammalian enzyme.
    Dooley KC; Applegarth DA
    J Inherit Metab Dis; 1980; 3(4):145-7. PubMed ID: 6787335
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Megadolichobasilar anomaly with thrombosis in a family with Fabry's disease and a novel mutation in the alpha-galactosidase A gene.
    Garzuly F; Maródi L; Erdös M; Grubits J; Varga Z; Gelpi E; Rohonyi B; Mázló M; Molnár A; Budka H
    Brain; 2005 Sep; 128(Pt 9):2078-83. PubMed ID: 15947062
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Fabry's disease: differentiation between two forms of -galactosidase by myoinositol.
    Crawhall JC; Banfalvi M
    Science; 1972 Aug; 177(4048):527-8. PubMed ID: 5050485
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Enzyme replacement therapy in patients with Fabry's disease.
    Tsuboi K
    J Int Med Res; 2007; 35(4):574-81. PubMed ID: 17697536
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Efficacy of replacement enzyme therapy on central nervous system manifestations in Fabry's disease].
    Besson G; Vadot W; Guellerin J
    Rev Med Interne; 2010 Dec; 31 Suppl 2():S257-9. PubMed ID: 21211675
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 8.