Fabry's diseaseHQSHOLT, L; WANDALL, A; SOÊRENSEN, S. A et al.Clinical genetics. 1989, Vol 36, Num 5, pp 335-336, issn 0009-9163, 2 p.Conference Paper

The effect of phlebotomy as a treatment of Fabry diseaseBEUTLER, E; WESTWOOD, B; DALE, G. L et al.Biochemical medicine. 1983, Vol 30, Num 3, pp 363-368, issn 0006-2944Article

Loss of electron-dense lamellar material from Fabrýs disease fibroblasts after enzyme replacementSIFERS, R. N; MAYES, J. S; NORDQUIST, R. E et al.Human genetics. 1983, Vol 65, Num 1, pp 85-87, issn 0340-6717Article

ConA-mediated binding and uptake of purified α-galactosidase A in Fabry fibroblastsHASHOLT, L; SØRENSEN, S. A.Experimental cell research. 1983, Vol 148, Num 2, pp 405-411, issn 0014-4827Article

CLINICAL AND DIAGNOSTIC CONSIDERATIONS IN FABRY'S DISEASEAHLMEN J; HULTBERG B; BRYNGER H et al.1982; ACTA MED. SCAND.; ISSN 0001-6101; SWE; DA. 1982; VOL. 211; NO 4; PP. 309-312; BIBL. 20 REF.Article

PROPERTIES OF IMMOBILIZED FIG ALPHA -GALACTOSIDASE AND EFFECT ON CERAMIDE-3 CONTENT OF PLASMA FROM PATIENTS WITH FABRY'S DISEASESCHRAM AW; HAMERS MN; OLDENBROEK HAVERKAMP E et al.1978; BIOCHIM. BIOPHYS. ACTA; NLD; DA. 1978; VOL. 527; NO 2; PP. 456-464; BIBL. 37 REF.Article

Enfermedad de Fabry. A propósito de una familia = Maladie de Fabry. Etude d'une famille = Fabry's disease. A family studyGUIZAR-VAZQUEZ, J; DEL PILAR CALVA-MERCADO, M; RODRIGUEZ-BUDELLI, M et al.Boletín médico del Hospital infantil de México (Spanish edition). 1985, Vol 42, Num 8, pp 494-496Article

Enzyme replacement in Fabry endothelial cells and fibroblasts: uptake experiments and electron microscopical studiesHASHOLT, L; WANDALL, A; SORENSEN, S. A et al.Clinical genetics. 1988, Vol 33, Num 5, pp 360-371, issn 0009-9163Article

Pathological study of the sural nerve in Fabry's diseaseGEMIGNANI, F; MARBINI, A; BRAGAGLIA, M. M et al.European neurology. 1984, Vol 23, Num 3, pp 173-181, issn 0014-3022Article

La maladie de Fabry = Fabry's diseaseCARSUZAA, F; ROMMEL, A; BOBIN, P et al.Annales de dermatologie et de vénéréologie. 1985, Vol 112, Num 8, pp 643-656, issn 0151-9638Article

A case of heterozygous Fabrýs disease with a short PR interval and giant negative T wavesYOKOYAMA, A; YAMAZOE, M; SHIBATA, A et al.British heart journal. 1987, Vol 57, Num 3, pp 296-299, issn 0007-0769Article

Fabry's disease in a heterozygous womanRODRIGUEZ, F. H. JR; HOFFMANN, E. O; ORDINARIO, A. T. JR et al.Archives of pathology & laboratory medicine (1976). 1985, Vol 109, Num 1, pp 89-91, issn 0363-0153Article

A 47-year-old man with coronary-artery disease and variable neurologic abnormalitiesDAWSON, D. M; MILLER, D. C.The New England journal of medicine. 1984, Vol 310, Num 2, pp 106-114, issn 0028-4793Article

Two dimensional echocardiographic similarity of Fabrýs disease to cardiac amyloidosis: a function of ultrastructural analogy?COHEN, I. S; FLURI-LUNDEEN, J; WHARTON, T. P et al.Journal of clinical ultrasound. 1983, Vol 11, Num 8, pp 437-441, issn 0091-2751Article

Fabry Disease and Cardiovascular Involvement : Anderson Fabry Disease: A Multiorgan Metabolic Disease Susceptible of TreatmentANASTASAKIS, Aris; PAPATHEODOROU, Efstathios; STERIOTIS, Alexandros Klavdios et al.Current pharmaceutical design (Print). 2013, Vol 19, Num 33, pp 5997-6008, issn 1381-6128, 12 p.Article

THE M-MODE ECHOCARDIOGRAM IN FABRY'S DISEASEBASS JL; SHRIVASTAVA S; GRABOWSKI GA et al.1980; AM. HEART J.; ISSN 0002-8703; USA; DA. 1980; VOL. 100; NO 6; PART. 1; PP. 807-812; BIBL. 9 REF.Article

ALPHA -GALACTOSIDASE ISOZYMES IN NORMAL INDIVIDUALS, AND IN FABRY HEMIZYGOTES AND HETEROZYGOTESSOERENSEN SA; HASHOLT L.1980; ANN. HUM. GENET.; GBR; DA. 1980; VOL. 43; NO 4; PP. 313-321; BIBL. 13 REF.Article

EVIDENCE FOR PREFERENTIAL X-CHROMOSOME INACTIVATION IN A FAMILY WITH FABRY DISEASE.ROPERS HH; WIENKER TF; GRIMM T et al.1977; AMER. J. HUM. GENET.; U.S.A.; DA. 1977; VOL. 29; NO 4; PP. 361-370; BIBL. 19 REF.Article

LA MALADIE DE FABRY CHEZ L'ENFANT. ETUDE CLINIQUE ET BIOLOGIQUE D'UNE FAMILLE. STRUCTURE ET ULTRASTRUCTURE DU REIN CHEZ UN HEMIZYGOTE ET UNE HETEROZYGOTE.DESBOIS JC; MAZIERE JC; GUBLER MC et al.1977; SEM. HOP., ANN. PEDIATR.; FR.; DA. 1977; VOL. 53; NO 8-9; PP. 575-586; ABS. ANGL. ESP.; BIBL. 2 P.Article

LES MANIFESTATIONS OPHTALMOLOGIQUES DE LA MALADIE DE FABRYDUFIER JL.1980; BULL. SOC. OPHTALMOL. FR.; ISSN 0081-1270; FRA; DA. 1980; VOL. 80; NO 12; PP. 1169-1171; BIBL. 8 REF.Article

ANDERSON-FABRY DISEASE AND DOWN'S SYNDROME: CASE REPORTGOSLING PJH.1979; J. MENTAL DEFIC. RES.; GBR; DA. 1979; VOL. 23; NO 3; PP. 187-188; BIBL. 7 REF.Article

DELAYED DIAGNOSIS IN ANGIOKERATOMA CORPORIS DIFFUSUM (ANDERSON-FABRY'S DISEASE).MITCHELL PC; TAAFFE A.1977; BRIT. MED. J.; G.B.; DA. 1977; NO 6053; PP. 83; BIBL. 5 REF.Article

THERAPEUTIC IMPLICATIONS OF RENAL TRANSPLANTATION IN A PATIENT WITH FABRY'S DISEASE.VAN DEN BERGH FAJTM; RIETRA PJGM; KOLK VEGTER AJ et al.1976; ACTA MED. SCAND.; SUEDE; DA. 1976; VOL. 200; NO 4; PP. 249-256; BIBL. 26 REF.Article

PROPERTIES OF MULTIPLE MOLECULAR FORMS OF ALPHA -GALACTOSIDASE AND ALPHA -N-ACETYLGALACTOSAMINIDASE FROM NORMAL AND FABRY LEUKOCYTESSALVAYRE R; MARET A; NEGRE A et al.1979; EUROP. J. BIOCHEM.; DEU; DA. 1979; VOL. 100; NO 2; PP. 377-383; BIBL. 38 REF.Article

ACCELERATED ATRIOVENTRICULAR CONDUCTION IN FABRY'S DISEASE: A CASE REPORTROWE JW; CARALIS DG.1978; ANGIOLOGY; USA; DA. 1978; VOL. 29; NO 7; PP. 562-568; BIBL. 11 REF.Article