BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

157 related articles for article (PubMed ID: 3128256)

  • 1. Severe orthostatic hypotension in a female carrier of Fabry's disease.
    Mutoh T; Senda Y; Sugimura K; Koike Y; Matsuoka Y; Sobue I; Takahashi A; Naoi M
    Arch Neurol; 1988 Apr; 45(4):468-72. PubMed ID: 3128256
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Corneal changes in Fabry's disease: a clinico-pathologic case report of a heterozygote.
    Macrae WG; Ghosh M; McCulloch C
    Ophthalmic Paediatr Genet; 1985 Apr; 5(3):185-90. PubMed ID: 3934620
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Biochemical and pathological studies on a carrier of Fabry's disease manifesting bouts of pain in the extremities].
    Katayama M; Kobayashi T; Ohnishi A; Goto I; Kuroiwa Y
    Rinsho Shinkeigaku; 1984 Jun; 24(6):575-80. PubMed ID: 6094070
    [No Abstract]   [Full Text] [Related]  

  • 4. Histopathologic findings of cornea verticillata in a woman heterozygous for Fabry's disease.
    Hirano K; Murata K; Miyagawa A; Terasaki H; Saigusa J; Nagasaka T; Kobayashi M
    Cornea; 2001 Mar; 20(2):233-6. PubMed ID: 11248839
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Contribution to Fabry's disease].
    Beck G
    Schweiz Med Wochenschr; 1980 Aug; 110(33):1190-201. PubMed ID: 6775369
    [No Abstract]   [Full Text] [Related]  

  • 6. Biopsy-proven cardiomyopathy in heterozygous Fabry's disease.
    Koitabashi N; Utsugi T; Seki R; Okamoto E; Sando Y; Kaneko Y; Nagai R
    Jpn Circ J; 1999 Jul; 63(7):572-5. PubMed ID: 10462028
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Nerve biopsy findings in hemizygous and heterozygous patients with Fabry's disease.
    Toyooka K; Said G
    J Neurol; 1997 Jul; 244(7):464-8. PubMed ID: 9266469
    [No Abstract]   [Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. Cerebrovascular manifestations in a female carrier of Fabry's disease.
    Grewal RP; McLatchey SK
    Acta Neurol Belg; 1992; 92(1):36-40. PubMed ID: 1546524
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Involvement of renal allograft by Fabry's disease.
    Popli S; Molnar ZV; Leehey DJ; Daugirdas JT; Roth DA; Adams MB; Cheng JC; Ing TS
    Am J Nephrol; 1987; 7(4):316-8. PubMed ID: 3120588
    [TBL] [Abstract][Full Text] [Related]  

  • 12. High incidence of thrombosis in Fabry's disease.
    Utsumi K; Yamamoto N; Kase R; Takata T; Okumiya T; Saito H; Suzuki T; Uyama E; Sakuraba H
    Intern Med; 1997 May; 36(5):327-9. PubMed ID: 9213168
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Fabry's disease in a heterozygous woman.
    Rodriguez FH; Hoffmann EO; Ordinario AT; Baliga M
    Arch Pathol Lab Med; 1985 Jan; 109(1):89-91. PubMed ID: 2982342
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Pure progressive autonomic failure presenting severe orthostatic hypotension.
    Akimitsu T; Maeda T; Hara M; Saikawa T; Takaki R; Sannomiya K; Okajima T
    Intern Med; 1993 Feb; 32(2):122-7. PubMed ID: 8507922
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Ultrastructural changes in the cornea and conjunctiva of a heterozygous woman with Fabry's disease.
    McCulloch C; Ghosh M
    Can J Ophthalmol; 1984 Jun; 19(4):192-8. PubMed ID: 6430531
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Renal transplantation in patients suffering from Fabry's disease. Kidney transplantation from an heterozygote subject to a subject without Fabry's disease].
    Grünfeld JP; Le Porrier M; Droz D; Bensaude I; Hinglais N; Crosnier J
    Nouv Presse Med; 1975 Sep; 4(29):2081-5. PubMed ID: 809752
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Possible mechanism of anhidrosis in a symptomatic female carrier of Fabry's disease: an assessment by skin sympathetic nerve activity and sympathetic skin response.
    Yamamoto K; Sobue G; Iwase S; Kumazawa K; Mitsuma T; Mano T
    Clin Auton Res; 1996 Apr; 6(2):107-10. PubMed ID: 8726095
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinical diagnosis of Fabry disease: whorl-like corneal opacity.
    Yoshikawa H; Ogawa I
    Neurology; 2003 Mar; 60(6):1048. PubMed ID: 12654983
    [No Abstract]   [Full Text] [Related]  

  • 19. Fabry's disease: report of a case.
    Chang HS; Ro LS; Chen ST; Tang LM; Hsiao KJ
    J Formos Med Assoc; 1995 Jun; 94(6):346-50. PubMed ID: 7549555
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A Fabry's disease heterozygote with a new mutation: biochemical, ultrastructural, and clinical investigations.
    Hasholt L; Sørensen SA; Wandall A; Andersen EB; Arlien-Søborg P
    J Med Genet; 1990 May; 27(5):303-6. PubMed ID: 2161929
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.