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kw.\*:("Sphingolipidose héréditaire Fabry")

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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

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

Clinipathological conference: a 29-Yr-Old man with recurrent episodes of fever, abdominal pain, and vomitingABREO, K; OBERLEY, T. D; GILBERT, E. F et al.American journal of medical genetics. 1984, Vol 18, Num 2, pp 249-264, issn 0148-7299Article

Ultrastructural changes in the cornea and conjunctiva of a heterozygous woman with Fabry's diseaseMCCULLOCH, C; MRINMAY GHOSH.Canadian journal of ophthalmology. 1984, Vol 19, Num 4, pp 192-198, issn 0008-4182Article

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

Metabolism of ceramide trihexoside in cultured skin fibroblasts from Fabry's patients, carriers and normal controlsKOBAYASHI, T; SHINNOH, N; KUROIWA, Y et al.Journal of the neurological sciences. 1984, Vol 65, Num 2, pp 169-177, issn 0022-510XArticle

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

ANALYTISCHE STUDIE DES MORBUS FABRY = ETUDE ANALYTIQUE DE LA MALADIE DE FABRYROTH J; SCHULZE E; RAABE G et al.1974; VIRCHOWS ARCH., A; DTSCH.; DA. 1974; VOL. 363; NO 3; PP. 287-301; ABS. ANGL.; BIBL. 2P.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

DETECTION AND PROPERTIES OF AN ACID ALPHA -GALACTOSIDASE (CERAMIDETRIHEXOSIDASE) IN NORMAL HUMAN URINERIETRA PJGM; TAGER JM; BORST P et al.1972; BIOCHIM. BIOPHYS. ACTA; PAYS-BAS; DA. 1972; VOL. 279; NO 3; PP. 436-445; BIBL. 24REF.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

MALADIE DE FABRYLAUGIER P; MACH RS; HUNZIKER N et al.1976; BULL. SOC. FR. DERMATOL. SYPHILIGR.; FR.; DA. 1976; VOL. 83; NO 2; PP. 88-89Article

UNE OBSERVATION D'ANGIOKERATOMA CORPORIS DIFFUSUM (MALADIE D'ANDERSON-FABRY)OLSZEWSKA Z; DEFECINSKA TRZECIAK E; ZEYDLER GRZEDZIELEWSKA L et al.1975; PRZEGL. DERMATOL.; POLSKA; DA. 1975; VOL. 62; NO 4; PP. 573-579; ABS. RUSSE ANGL.; BIBL. 22 REF.Article

DIE FABRYSCHE KRANKHEIT (ANGIOKERATOMA CORPORIS DIFFUSUM) = LA MALADIE DE FABRY (ANGIOKERATOME CORPOREL DIFFUS)BREZINA Z.1974; KINDERAERZTL. PRAXIS; DTSCH.; DA. 1974; VOL. 42; NO 4; PP. 159-161Article

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

A PROPOS D'UN CAS DE MALADIE DE FABRY.FERRACCI C; BALTENNECK A; ANTIGLIO V et al.1977; MED. ET ARMEES; FR.; DA. 1977; VOL. 5; NO 10; PP. 893-896; BIBL. 11 REF.Article

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