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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

ANGIOKERATOMA CORPORIS DIFFUSUM: THE EVOLUTION OF A DISEASE ENTITY.TAAFFE A.1977; POSTGRAD. MED. J.; G.B.; DA. 1977; VOL. 53; NO 616; PP. 78-81; BIBL. 19 REF.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

MORBUS ANDERSON-FABRY (ANGIOKERATOMA CORPORIS DIFFUSUM) = MALADIE D'ANDERSON FABRY (ANGIOKERATOME DIFFUS)FODOR D; ZSAMBEKI P; SCHNEIDER I et al.1983; H+G. ZEITSCHRIFT FUER HAUTKRANKHEITEN; ISSN 0301-0481; DEU; DA. 1983; VOL. 58; NO 13; PP. 951-958; 6 P.; ABS. ENG; BIBL. 18 REF.Article

DIFFERENTIAL ASSAY FOR LYSOSOMAL ALPHA-GALACTOSIDASES IN HUMAN TISSUES AND ITS APPLICATION TO FABRY'S DISEASEMAYES JS; SCHEERER JB; SIFERS RN et al.1981; CLIN. CHIM. ACTA; ISSN 0009-8981; NLD; DA. 1981; VOL. 112; NO 2; PP. 247-251; BIBL. 19 REF.Article

BEITRAG ZUR FABRYSCHEN KRANKHEIT = CONTRIBUTION SUR LA MALADIE DE FABRYBECK G.1980; SCHWEIZ. MED. WSCHR.; CHE; DA. 1980; VOL. 110; NO 33; PP. 1190-1201; ABS. ENG; BIBL. 54 REF.Article

CHARACTERIZATION OF ALPHA -GALACTOSIDASE ISOENZYMES IN NORMAL AND FABRY HUMAN-CHINESE HAMSTER SOMATIC CELL HYBRIDS.HAMERS MN; WESTERVELD A; MEERA KHAN et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 36; NO 3; PP. 289-297; BIBL. 1 P. 1/2Article

MALADIE DE FABRY, NOUVELLE VARIANTE (A PROPOS DE DEUX CAS FAMILIAUX AVEC TAUX D'ALPHA GALACTOSIDASE NORMAL).BEUREY J; WEBER M; CARTAULT F et al.1977; ANN. MED. NANCY; FR.; DA. 1977-04; VOL. 16; PP. 491-496 (5P.); ABS. ANGL.; BIBL. 1 REF.Article

LA MALADIE DE FABRY. TRAITEMENT DU SYNDROME ACRODYNIFORME PAR LA CARBAMAZEPINE.LENOIR G; RIVRON M; GUBLER MC et al.1977; ARCH. FR. PEDIATR.; FR.; DA. 1977; VOL. 34; NO 8; PP. 704-716; ABS. ANGL.; BIBL. 1 P.Article

DIAGNOSTIC DE LA MALADIE DE FABRY.ULMANN A; LENOIR G; BAUMANN N et al.1976; NOUV. PRESSE MED.; FR.; DA. 1976; VOL. 5; NO 40; PP. 2697-2700; ABS. ANGL.; BIBL. 16 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

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

Fabrýs disease (angiokeratoma corporis diffusum universale): ocular and associated findingsMAINO, J. H.Journal of the American Optometric Association. 1983, Vol 54, Num 12, pp 1061-1065, issn 0003-0244Article

ETUDE, PAR TRANSFORMATION DE FOURIER OPTIQUE, DES DEPOTS DE GLYCOLIPIDES DANS LE CAS DE LA MALADIE DE FABRYDUPOISOT H; CONSTANS A; DAURY G et al.1979; C.R. ACAD. SCI., D; FRA; DA. 1979; VOL. 288; NO 8; PP. 783-786; ABS. ENG; BIBL. 10 REF.Article

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ENZYMOLOGICAL PROPERTIES AND IMMUNOLOGICAL CHARACTERIZATION OF ALPHA -GALACTOSIDASE ISOENZYMES FROM NORMAL AND FABRY HUMAN LIVER.SCHRAM AW; HAMERS MN; BROUWER KELDER B et al.1977; BIOCHIM. BIOPHYS. ACTA; PAYS-BAS; DA. 1977; VOL. 482; NO 1; PP. 125-137; BIBL. 27 REF.Article