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5. 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]
6. 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]
7. Fabry's disease. Kato H; Sato K; Hattori S; Ikemoto S; Shimizu M; Isogai Y Intern Med; 1992 May; 31(5):682-5. PubMed ID: 1324036 [TBL] [Abstract][Full Text] [Related]
8. Fabry's disease. Adam T; Alexandrescu L; Voinea F; Toringhibel M; Hâncu A Rom J Intern Med; 2006; 44(4):455-64. PubMed ID: 18386622 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. [Fabry's disease: diagnosis in the pediatric age group]. Pintos Morell G An Esp Pediatr; 2002 Jul; 57(1):45-50. PubMed ID: 12139892 [TBL] [Abstract][Full Text] [Related]
16. [Fabry's disease and hypoparathyroidism]. Misery L; Gregoire M; Prieur F; Froissart R; Guffon N; Maitre S; Fond L; Denis L; Perrot JL; Cambazard F Ann Med Interne (Paris); 2002 Jun; 153(4):283-5. PubMed ID: 12218896 [TBL] [Abstract][Full Text] [Related]
17. [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]
18. [Cardiac manifestations of Fabry's disease]. Han ZH; Jiang TY; Ren XJ; Wu XS; Zhang WD; Chen F Zhonghua Nei Ke Za Zhi; 2009 Jun; 48(6):462-4. PubMed ID: 19954039 [TBL] [Abstract][Full Text] [Related]
19. Fabry's disease. A brief review in connection with a Scandinavian survey. Helin I Scand J Urol Nephrol; 1979; 13(3):335-7. PubMed ID: 119314 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]