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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. [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]
4. [Ocular findings in Fabry's disease]. Kuzman T; Juri J; Mrsić M; Jeren-Strujić B; Mandić Z; Sikić J Acta Med Croatica; 2006; 60(2):163-6. PubMed ID: 16848212 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. [Diagnosis of Fabry's disease]. Mendel'son MM; Livandovskiĭ IuA; Vidershaĭn GIa; Bruk EI; Il'ina GS Ter Arkh; 1987; 59(8):137-41. PubMed ID: 3120344 [No Abstract] [Full Text] [Related]
7. [A case of Fabry's disease detected by renal biopsy findings]. Yamada S; Ito H; Ohashi T; Yasumoto Y; Yamashita W; Harada R; Arima T; Osaki K; Nakashima A; Maeda T Fukuoka Igaku Zasshi; 1990 Aug; 81(8):266-70. PubMed ID: 2172129 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. Clinical, histopathological, and biochemical findings in Fabry's disease. A case report and family study. Savi M; Olivetti G; Neri TM; Curtoni C Arch Pathol Lab Med; 1977 Oct; 101(10):536-9. PubMed ID: 199133 [TBL] [Abstract][Full Text] [Related]
10. Atypical Fabry's disease. An oligosymptomatic variant. Ko YH; Kim HJ; Roh YS; Park CK; Kwon CK; Park MH Arch Pathol Lab Med; 1996 Jan; 120(1):86-9. PubMed ID: 8554452 [TBL] [Abstract][Full Text] [Related]
11. Association of renal ectopia with Fabry's disease in 3 patients. Rákóczi E; Tóth B; Görögh S; Erdos M; Sümegi J; Maródi L J Urol; 2009 Apr; 181(4):1949-54. PubMed ID: 19237168 [TBL] [Abstract][Full Text] [Related]
12. [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]
13. Subclinical Fabry's disease occurring in the context of IgA nephropathy. Kawamura O; Sakuraba H; Itoh K; Suzuki Y; Doi M; Kuwabara H; Oshima S; Abe S; Warabi H; Yoshizawa N Clin Nephrol; 1997 Feb; 47(2):71-5. PubMed ID: 9049452 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. A case of Fabry's disease. Miura M; Tomino Y; Inoue W; Endoh M; Suga T; Kaneshige H; Nomoto Y; Sakai H; Matsuo I; Nagura H; Ikeda N Tokai J Exp Clin Med; 1983 Jan; 8(1):23-9. PubMed ID: 6310828 [TBL] [Abstract][Full Text] [Related]
16. [Fabry's disease; towards a treatment]. Linthorst GE; Hollak CE; Bosman DK; Heymans HS; Aerts JM Ned Tijdschr Geneeskd; 2000 Dec; 144(50):2391-5. PubMed ID: 11145093 [TBL] [Abstract][Full Text] [Related]
18. A case of multiple angiomas without any angiokeratomas in a female heterozygote with Fabry disease. Mirceva V; Hein R; Ring J; Möhrenschlager M Australas J Dermatol; 2010 Feb; 51(1):36-8. PubMed ID: 20148840 [TBL] [Abstract][Full Text] [Related]
19. [Postmortem diagnosis of Fabry disease in a female heterozygote leading to the detection of undiagnosed manifest disease in the family]. Hůlková H; Ledvinová J; Poupĕtová H; Bultas J; Zeman J; Elleder M Cas Lek Cesk; 1999 Nov; 138(21):660-4. PubMed ID: 10746023 [TBL] [Abstract][Full Text] [Related]