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

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

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

MALADIE DE FABRY (ANGIOKERATOMA CORPORIS DIFFUSUMBREZINA Z.1975; CESKOSL. PEDIATR.; CESKOSL.; DA. 1975; VOL. 30; NO 6; PP. 288-289; ABS. RUSSE ANGL.; BIBL. 3 REF.Article

BIOCHEMICAL AND GENETIC STUDIES IN TWO FAMILIES WITH FABRY DISEASE = ETUDES BIOCHIMIQUES ET GENETIQUES DANS 2 FAMILLES PRESENTANT UNE MALADIE DE FABRYGOTO I; TABIRA T; NAWA A et al.1974; ARCH. NEUROL.; U.S.A.; DA. 1974; VOL. 31; NO 1; PP. 45-50; BIBL. 26REF.Article

ROENTGENO-ODDITIES = CURIOSITES RADIOLOGIQUES1973; ORAL SURG. ORAL MED. ORAL PATHOL.; U.S.A.; DA. 1973; VOL. 35; NO 3; PP. 432-434Serial Issue

MALADIE DE FABRY. ETUDE ULTRASTRUCTURALEPERROT H; SCHMITT D; THIVOLET J et al.1973; LYON MED.; FR.; DA. 1973; VOL. 229; NO 6; PP. 581-589; ABS. ANGL.; BIBL. 1 P.Serial Issue

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

METABOLISM OF NEUTRAL GLYCOSPHINGOLIPIDS IN PLASMA OF A NORMAL HUMAN AND A PATIENT WITH FABRY'S DISEASE.VANCE DE; KRIVIT W; SWEELEY CC et al.1975; J. BIOL. CHEM.; U.S.A.; DA. 1975; VOL. 250; NO 20; PP. 8119-8125; BIBL. 29 REF.Article

LA TRANSPLANTATION RENALE CHEZ LES SUJETS ATTEINTS DE MALADIE DE FABRY. TRANSPLANTATION DU REIN D'UN SUJET HETEROZYGOTE A UN SUJET SAIN.GRUNFELD JP; LE PORRIER M; DROZ D et al.1975; NOUV. PRESSE MED.; FR.; DA. 1975; VOL. 4; NO 29; PP. 2081-2085; ABS. ANGL.; BIBL. 27 REF.Article

LOSS OF SMALL PERIPHERAL SENSORY NEURONS IN FABRY DISEASE. HISTOLOGIC AND MORPHOMETRIC EVALUATION OF CUTANEOUS NERVES, SPINAL GANGLIA, AND POSTERIOR COLUMNS = LYSE DES PETITS NEURONES SENSORIELS PERIPHERIQUES DANS LA MALADIE DE FABRY. ANALYSE HISTOLOGIQUE ET MORPHOMETRIQUE DES NERFS CUTANES, DES GANGLIONS MEDULLAIRES ET DES FAISCEAUX POSTERIEURSOHNISHI A; DYCK PJ.1974; ARCH. NEUROL.; U.S.A.; DA. 1974; VOL. 31; NO 2; PP. 120-127Article

A NEW ETIOLOGY OF PRIAPISM: FABRY'S DISEASE = UNE NOUVELLE ETIOLOGIE DU PRIAPISME, LA MALADIE DE FABRYWILSON SK; KLIONSKY BL; RHAMY RK et al.1973; J. UROL.; U.S.A.; DA. 1973; VOL. 109; NO 4; PP. 646-648; BIBL. 8REF.Article

LA MALADIE DE FABRY, ETUDE HISTOLOGIQUE ET ULTRASTRUCTURALE.PAQUIN JG; CAMIRAND P; MANDALENAKIS N et al.1975; UN. MED. CANADA; CANADA; DA. 1975; VOL. 104; NO 9; PP. 1377-1382; ABS. ANGL.; BIBL. 21 REF.Article

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

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

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

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

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