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 *

96 related articles for article (PubMed ID: 2166184)

  • 1. Identification of Fabry disease in two brothers.
    Beyer E; Djatlovitskaya E; Zairatyants O; Berestova A; Mendelson M; Brook E; Wiederschain G
    J Inherit Metab Dis; 1990; 13(2):230-1. PubMed ID: 2166184
    [No Abstract]   [Full Text] [Related]  

  • 2. [Biochemical diagnosis of Anderson-Fabry disease in two brothers].
    Vidershaĭn GIa; Beĭer EM; Mendel'son MM; Livandovskiĭ IuA
    Vopr Med Khim; 1986; 32(5):120-3. PubMed ID: 3095985
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Pseudodeficiency of alpha-galactosidase A.
    Bach G; Rosenmann E; Karni A; Cohen T
    Clin Genet; 1982 Jan; 21(1):59-64. PubMed ID: 6279339
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Fabry disease: systemic deposition of a glycolipid].
    Sela BA; Pavlotsky F; Trau H; Kaplan B; Polak-Charcon S; Engelberg S
    Harefuah; 1994 Sep; 127(5-6):157-60, 215. PubMed ID: 7995582
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Pseudo-clinical Fabry's disease without alpha galactosidase deficiency.
    Peltier A; Herbeuval E; Brondeau MT; Belleville F; Nabet P
    Biomedicine; 1977 May; 26(3):194-201. PubMed ID: 407951
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Urinary ultrastructural findings in Fabry disease.
    Katz SM; Lyons PJ
    JAMA; 1977 Mar; 237(11):1121-2. PubMed ID: 402489
    [No Abstract]   [Full Text] [Related]  

  • 8. The biochemistry of sphingolipid storage diseases.
    Sandhoff K
    Angew Chem Int Ed Engl; 1977 May; 16(5):273-85. PubMed ID: 406814
    [No Abstract]   [Full Text] [Related]  

  • 9. [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]  

  • 10. Fabry cardiomyopathy in the female confirmed by endomyocardial biopsy.
    Broadbent JC; Edwards WD; Gordon H; Hartzler GO; Krawisz JE
    Mayo Clin Proc; 1981 Oct; 56(10):623-8. PubMed ID: 6268901
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Letter: Angiokeratoma corporis diffusum and lysosomal enzyme deficiency.
    Loonen MC; Lugt L; Franke CL
    Lancet; 1974 Sep; 2(7883):785. PubMed ID: 4143049
    [No Abstract]   [Full Text] [Related]  

  • 12. Diagnosis of inherited enzymatic deficiencies with tears: Fabry disease.
    Del Monte MA; Johnson DL; Cotlier E; Desnick RJ
    Birth Defects Orig Artic Ser; 1976; 12(3):209-19. PubMed ID: 8173
    [No Abstract]   [Full Text] [Related]  

  • 13. [Fabry-Anderson's disease].
    Andratschke C
    Fortschr Med; 1975 Dec; 93(34):1697-702. PubMed ID: 811519
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Biochemical and genetic studies in two families with Fabry disease.
    Goto I; Tabira T; Nawa A; Kurokawa T; Kuroiwa Y
    Arch Neurol; 1974 Jul; 31(1):45-50. PubMed ID: 4209573
    [No Abstract]   [Full Text] [Related]  

  • 15. [Procedure for the diagnosis of sphingolipidoses or allied diseases in adult patients with neurological or psychiatric symptoms (author's transl)].
    Pilz H; Heipertz R; Seidel D
    Nervenarzt; 1979 Dec; 50(12):749-61. PubMed ID: 94938
    [No Abstract]   [Full Text] [Related]  

  • 16. Attempt at enzyme replacement by fetal liver transplantation in Fabry's disease.
    Touraine JL; Malik MC; Traeger J; Perrot H; Maire I
    Lancet; 1979 May; 1(8125):1094-5. PubMed ID: 86827
    [No Abstract]   [Full Text] [Related]  

  • 17. Heterozygote detection in Fabry disease utilizing multiple enzyme activities.
    Sheth KJ; Good TA; Murphy JV
    Am J Med Genet; 1981; 10(2):141-6. PubMed ID: 6274191
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Intestinal manifestations of Fabry's disease.
    Rowe JW; Gilliam JI; Warthin TA
    Ann Intern Med; 1974 Nov; 81(5):628-31. PubMed ID: 4214387
    [No Abstract]   [Full Text] [Related]  

  • 19. 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]  

  • 20. [Fabry disease: diagnostic due of substitutive enzyme-therapy].
    Barbey F; Widmer U; Burnier M; Lidove O
    Rev Med Suisse Romande; 2002 Sep; 122(9):449-53. PubMed ID: 12422475
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.