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Results 1 to 25 of 631

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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

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

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

LINKAGE RELATIONSHIP OF THE LOCI FOR ANDERSON-FABRY DISEASE AND THE XG BLOOD GROUPSJOHNSTON AW; SANGER R.1981; ANN. HUM. GENET.; ISSN 0003-4800; GBR; DA. 1981; VOL. 45; PART. 2; PP. 155-157; BIBL. 12 REF.Article

MALADIE DE FABRY ANGIOKERATOME: INTERET DIAGNOSTIQUE DE L'ETUDE ULTRASTRUCTURALE DE LA PEAULE CHARPENTIER Y; CROUZET J; LE CHARPENTIER M et al.1981; SEM. HOP.; ISSN 0037-1777; FRA; DA. 1981; VOL. 57; NO 1-2; PP. 78-82; ABS. ENG; BIBL. 22 REF.Article

MORPHOLOGIE CRISTALLINE DES DEPOTS DE TRIHEXOSYLCERAMIDES CARACTERISTIQUES DE LA MALADIE DE FABRY (FORME RHUMATISMALE NOTAMMENT)LAOUSSADI S; DUPOISOT H; CONSTANS A et al.1981; C.R. SOC. BIOL. FIL; ISSN 0037-9026; FRA; DA. 1981; VOL. 175; NO 1; PP. 55-67; H.T. 5; BIBL. 6 REF.Article

ANGIOQUERATOSIS DE FABRY: PRESENTACION DE UN CASO Y REVISION DE LA LITERATURA = ANGIOKERATOSE DE FABRY: PRESENTATION D'UN CAS ET REVUE DE LA LITTERATUREGARCIA RAMON RJ; ROSALEN R; CHORDA D et al.1980; REV. CLIN. ESP.; ESP; DA. 1980; VOL. 156; NO 3; PP. 207-212; BIBL. 36 REF.Article

CONTRIBUTION A L'ETUDE DE LA MALADIE DE FABRY CHEZ L'ENFANT. A PROPOS D'UN CAS PERSONNEL REVELE PAR UN SYNDROME POLYUROPOLYDIPSIQUEGUEHO ANDRE.1979; ; FRA; LYON: I.C. VAUBECOUR; DA. 1979; 19; 187 P.; 30 CM; BIBL. 212 REF.; TH.: MED./LYON 1/1979Thesis

CORNEAL ULTRASTRUCTURAL CHANGES IN FABRY'S DISEASEFRANCOIS J; HANSSENS M; TEUCHY H et al.1978; OPHTHALMOLOGICA; CHE; DA. 1978; VOL. 176; NO 6; PP. 313-330; ABS. GER/FRE; BIBL. 43 REF.Article

FABRY'S DISEASE: BIOCHEMICAL AND HISTOCHEMICAL STUDIES ON HAIR ROOTS FOR CARRIER DETECTION.VERMORKEN AJM; WETERINGS PJJM; SPIERENBURG GT et al.1978; BRIT. J. DERMATOL.; G.B.; DA. 1978; VOL. 98; NO 2; PP. 191-196; BIBL. 8 REF.Article

ENZYME REPLACEMENT THERAPY IN GAUCHER'S AND FABRY'S DISEASE.PENTCHEV PG.1977; ANN. CLIN. LAB. SCI.; U.S.A.; DA. 1977; VOL. 7; NO 3; PP. 251-253; BIBL. 5 REF.Article

NEFROPATIA SENZA SINTOMI URINARI IN UN CASO DI MALATTIA DI FABRY CLINICAMENTE ATIPICO. STUDIO CLINICO E BIOCHIMICO DI UN NUCLEO FAMILIARE. = NEPHROPATHIE SANS SYMPTOMES URINAIRES DANS UN CAS DE MALADIE DE FABRY CLINIQUEMENT ATYPIQUE. ETUDE CLINIQUE ET BIOCHIMIQUE D'UN NOYAU FAMILIALPANNARALE G; MICELLI M; RIZZI R et al.1977; MINERVA NEFROL.; ITAL.; DA. 1977; VOL. 24; NO 5; PP. 405-410; ABS. ANGL.; BIBL. 26 REF.Article

CONTRIBUTION A L'ETUDE DE L'ANGIOKERATOMA CORPORIS DIFFUSUM DE FABRYSEBA NOUREDDINE.sd; FRA; DA. S.D.; 153-IXL P.; 30 CM; BIBL. 437 REF.; TH.: MED./ALGER/1977Thesis

ANGIOKERATOMA CORPORIS DIFFUSUM (MORBUS FABRY) = ANGIOKERATOME CORPOREL DIFFUS (MALADIE DE FABRY)BOEHM G.1981; AKTUEL. DERMATOL.; ISSN 0340-2541; DEU; DA. 1981; VOL. 7; NO 4; PP. 99-101; ABS. ENG; BIBL. 13 REF.Article

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