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 *

119 related articles for article (PubMed ID: 3095985)

  • 21. 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]  

  • 22. [Diffuse Fabry's angiokeratoma].
    Trofimova IB; Aĭvazian AA
    Vestn Dermatol Venerol; 1983 Jan; (1):54-7. PubMed ID: 6299021
    [No Abstract]   [Full Text] [Related]  

  • 23. [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]  

  • 24. Screening patients with hypertrophic cardiomyopathy for Fabry disease using a filter-paper test: the FOCUS study.
    Hagège AA; Caudron E; Damy T; Roudaut R; Millaire A; Etchecopar-Chevreuil C; Tran TC; Jabbour F; Boucly C; Prognon P; Charron P; Germain DP;
    Heart; 2011 Jan; 97(2):131-6. PubMed ID: 21062768
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Molecular genetics of inherited metabolic diseases--its application to the investigation of pathogenesis and the diagnosis of Fabry disease].
    Sakuraba H
    Rinsho Byori; 1994 Jun; 42(6):628-35. PubMed ID: 7914243
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Letter: Diagnosis of Fabry's disease by tear alpha-galactosidase A.
    Del Monte MA; Johnson DL; Cotlier E; Krivit W; Desnick RJ
    N Engl J Med; 1974 Jan; 290(1):57-8. PubMed ID: 4202326
    [No Abstract]   [Full Text] [Related]  

  • 27. In vitro study of encapsulation therapy for Fabry disease using genetically engineered CHO cell line.
    Naganawa Y; Ohsugi K; Kase R; Date I; Sakuraba H; Sakuragawa N
    Cell Transplant; 2002; 11(4):325-9. PubMed ID: 12162373
    [TBL] [Abstract][Full Text] [Related]  

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

  • 29. Later-onset Fabry disease: an adult variant presenting with the cramp-fasciculation syndrome.
    Nance CS; Klein CJ; Banikazemi M; Dikman SH; Phelps RG; McArthur JC; Rodriguez M; Desnick RJ
    Arch Neurol; 2006 Mar; 63(3):453-7. PubMed ID: 16533976
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A successful approach for the detection of Fabry patients in Argentina.
    Rozenfeld PA; Tarabuso A; Ebner R; Ramallo G; Fossati CA
    Clin Genet; 2006 Apr; 69(4):344-8. PubMed ID: 16630168
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Fabry disease: clinical, biochemical and electron microscopical studies (author's transl)].
    Klug H; Zabel R; Evers U
    Dermatol Monatsschr; 1979 Jan; 165(1):46-54. PubMed ID: 220105
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Anderson-Fabry disease].
    Kes P; Basić-Jukić N; Brunetta B; Jurić I
    Acta Med Croatica; 2006; 60(1):55-8. PubMed ID: 16802573
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Direct comparison of enzyme measurements from dried blood and leukocytes from male and female Fabry disease patients.
    Lukacs Z; Hartung R; Beck M; Keil A; Mengel E
    J Inherit Metab Dis; 2007 Aug; 30(4):614. PubMed ID: 17694354
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Enzymatic corrections for cells derived from Fabry disease patients by a recombinant adenovirus vector.
    Ohsugi K; Kobayashi K; Itoh K; Sakuraba H; Sakuragawa N
    J Hum Genet; 2000; 45(1):1-5. PubMed ID: 10697955
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The use of conjunctival biopsy and enzyme analysis in tears for the diagnosis of homozygotes and heterozygotes with Fabry disease.
    Libert J; Tondeur M; Van Hoof F
    Birth Defects Orig Artic Ser; 1976; 12(3):221-39. PubMed ID: 821559
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Anderson-Fabry disease with cerebrovascular complications in two Italian families.
    Borsini W; Giuliacci G; Torricelli F; Pelo E; Martinelli F; Scordo MR
    Neurol Sci; 2002 Jun; 23(2):49-53. PubMed ID: 12235491
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Basilar artery aneurysm and Anderson-Fabry disease.
    Maisey DN; Cosh JA
    J Neurol Neurosurg Psychiatry; 1980 Jan; 43(1):85-7. PubMed ID: 6766499
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Misdiagnosis of Fabry disease: importance of biochemical confirmation of clinical or pathological suspicion.
    Linthorst GE; De Rie MA; Tjiam KH; Aerts JM; Dingemans KP; Hollak CE
    Br J Dermatol; 2004 Mar; 150(3):575-7. PubMed ID: 15030345
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [alpha-Galactosidase gene mutation and its expression product in Fabry disease (alpha-galactosidase deficiency)].
    Okumiya T; Takata T; Sasaki M; Sakuraba H
    Rinsho Byori; 1997 Feb; 45(2):127-35. PubMed ID: 9120996
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Quantification of α-galactosidase activity in intact leukocytes.
    Hölzl MA; Gärtner M; Kovarik JJ; Hofer J; Bernheimer H; Sunder-Plassmann G; Zlabinger GJ
    Clin Chim Acta; 2010 Nov; 411(21-22):1666-70. PubMed ID: 20599861
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.