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GANGLIOSIDE STORAGE DISEASES = LES GANGLIOSIDOSESO'BRIEN JS.1972; ADV. HUM. GENET.; U.S.A.; DA. 1972; VOL. 3; PP. 39-434 (60P.); H.T. 1; BIBL. 4P.Serial Issue

DIFFERENTIALDIAGNOSE ANGEBORENER LIPIDOSEN DURCH LIPIDANALYSEN VON KOERPERFLUESSIGKEITEN, BIOPSIE- UND AUTOPSIEGEWEBE. = DIAGNOSTIC DIFFERENTIEL DES LIPIDOSES HEREDITAIRES PAR L'ANALYSE LIPIDIQUE DES LIQUIDES ORGANIQUES, DE LA BIOPSIE ET DES TISSUS PRELEVES A L'AUTOPSIEPILZ H; HEIPERTZ R.1975; FORTSCHR. NEUROL. PSYCHIATR. GRENZGEB.; DTSCH.; DA. 1975; VOL. 43; NO 11; PP. 602-617; BIBL. 2 P. 1/2Article

GM1 GANGLIOSIDOSIS IN SKIN FIBROBLAST CULTURE. ENZYMATIC DIFFERENCES BETWEEN TYPES1 AND 2 AND OBSERVATIONS ON A THIRD VARIANT = GANGLIOSIDOSE GM1 ET CULTURES DE FIBROBLASTES CUTANES: DIFFERENCES ENZYMATIQUES ENTRE LES TYPES 1 ET 2 ET OBSERVATION D'UNE TROISIEME VARIANTEPINSKY L; MILLER J; SHANFIELD B et al.1974; AMER. J. HUM. GENET.; U.S.A.; DA. 1974; VOL. 26; NO 5; PP. 563-577; BIBL. 1P.Serial Issue

DIFFERENTIATION OF TWO VARIANTS OF TYPE-AB GM2 GANGLIOSIDOSIS USING CHROMOGENIC SUBSTRATESYU TEH LI; HIRABAYASHI Y; SU CHEN LI et al.1983; AMERICAN JOURNAL OF HUMAN GENETICS; ISSN 0002-9297; USA; DA. 1983; VOL. 35; NO 3; PP. 520-522; BIBL. 8 REF.Article

IDENTIFICATION OF A POSSIBLE SUBUNIT OF HEXOSAMINIDASE A AND B = IDENTIFICATION D'UNE SOUS-UNITE POSSIBLE DES HEXOSAMINIDASES A ET BROBINSON D; CARROLL M; STIRLING JL et al.1973; NATURE; G.B.; DA. 1973; VOL. 243; NO 5407; PP. 415-416; BIBL. 11REF.Serial Issue

CHARACTERIZATION OF OLIGOSACCHARIDES AND GLYCOPEPTIDES EXCRETED IN THE URINE OF GM1-GANGLIOSIDOSIS PATIENTS.NG YING KIN; WOLFE LS.1975; BIOCHEM. BIOPHYS. RES. COMMUNIC.; U.S.A.; DA. 1975; VOL. 66; NO 1; PP. 123-130; BIBL. 23 REF.Article

HEXOSAMINIDASE-A AND HEXOSAMINIDASE-B: STUDIES IN TAY-SACHS'AND SANDHOFF'S DISEASE = HEXOSAMINIDASEA ET HEXOSAMINIDASEB: ETUDES DANS LA MALADIE DE TAY-SACHS ET DANS CELLE DE SANDHOFFSRIVASTAVA SK; BEUTLER E.1973; NATURE; G.B.; DA. 1973; VOL. 241; NO 5390; PP. 463; BIBL. 9REF.Serial Issue

ENZYMATIC STUDY OF GM1 GANGLIOSIDOSIS = ETUDE ENZYMATIQUE DE LA GANGLIOSIDOSE GM1YUTAKA T; OKADA S; MIMAKI K et al.1975; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1975; VOL. 59; NO 3; PP. 283-290; BIBL. 16REF.Article

JUVENILE GM1 GANGLIOSIDOSIS. OCCURRENCE WITH ABSENCE OF TWO BETA -GALACTOSIDASE COMPONENTS = GANGLIOSIDOSE GM1 JUVENILE. SURVENUE AVEC L'ABSENCE DE DEUX COMPOSANTES BETA -GALACTOSIDASELOWDEN JA; CALLAHAN JW; NORMAN MG et al.1974; ARCH. NEUROL.; U.S.A.; DA. 1974; VOL. 31; NO 3; PP. 200-203; BIBL. 20REF.Article

BRAIN GLYCOLIPIDS IN TWO TYPES OF INFANTILE AMAUROTIC IDIOTSNAOI M; KLENK E.1972; Z. (HOPPE-SEYLER'S) PHYSIOL. CHEM.; DTSCH.; DA. 1972; VOL. 353; NO 11; PP. 1684-1694; ABS. ALLEM.; BIBL. 21REF.Serial Issue

Diagnosis of infantile and juvenile forms of GM2 gangliosidosis variant 0: residual activities toward natural and different synthetic substratesKYTZIA, H.-J; HINRICHS, U; SANDHOFF, K et al.Human genetics. 1984, Vol 67, Num 4, pp 414-418, issn 0340-6717Article

Assay of the G M2-ganglioside cleaving hexosaminidase activity of skin fibroblasts for G M2-gangliosidosesHARZER, K.Clinica chimica acta. 1983, Vol 135, Num 1, pp 89-93, issn 0009-8981Article

Regional variation of brain gangliosides in feline GM1 gangliosidosisBYRNE, M. C; LEDEEN, R. W.Experimental neurology (Print). 1983, Vol 81, Num 1, pp 210-225, issn 0014-4886Article

DEFICIENT GANGLIOSIDE BIOSYNTHESIS: A NOVEL HUMAN SPHINGOLIPIDOSIS = BIOSYNTHESE DEFICIENTE DE GANGLIOSIDES: NOUVELLE SPHINGOLIPIDOSE HUMAINEFISHMAN PH; MAX SR; TALLMAN JF et al.1975; SCIENCE; U.S.A.; DA. 1975; VOL. 187; NO 4171; PP. 68-70; BIBL. 15REF.Article

ALTERED LEVELS OF TISSUE GANGLIOSIDES AND GLYCOPROTEINS IN THE INFANTILE FORM OF GM1-GANGLIOSIDOSIS = MODIFICATIONS DES TAUX DE GANGLIOSIDES ET GLYCOPROTEINES TISSULAIRES DANS LA FORME INFANTILE DE LA GANGLIOSIDOSE GM1BERRA B; DI PALMA S; BRUNNGRABER EG et al.1974; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1974; VOL. 57; NO 3; PP. 301-306; BIBL. 10REF.Article

LA GANGLIOSIDOSE A GMI (TYPE 1) A PROPOS DE DEUX OBSERVATIONS PERSONNELLESGOUEDARD HERVE.sd; FRA; DA. S.D.; 29293; 61 P.-PL.; 30 CM; BIBL. 199 REF.; TH.: MED./BREST/1977Thesis

Juvenile GM2 gangliosidosis (AuMB variant): inability to activate hexosaminidase A by activator proteinINUI, K; GREBNER, E. E; JACKSON, L. G et al.American journal of human genetics. 1983, Vol 35, Num 4, pp 551-564, issn 0002-9297Article

STRUCTURE OF THE GLYCOPEPTIDE STORAGE MATERIAL IN GM1 GANGLIOSIDOSIS. SEQUENCE DETERMINATION WITH SPECIFIC ENDO- AND EXOGLYCOSIDASESCHEN TSAY G; DAWSON G; YU TEH LI et al.1975; BIOCHIM. BIOPHYS. ACTA; PAYS-BAS; DA. 1975; VOL. 385; NO 2; PP. 305-311; BIBL. 25REF.Article

AN ELECTROPHORETIC VARIANT OF BETA -GALACTOSIDASE WITH ALTERED CATALYTIC PROPERTIES IN A PATIENT WITH GM1 GANGLIOSIDOSISNORDEN AGW; O'BRIEN JS.1975; PROC. NATION. ACAD. SCI. U.S.A.; U.S.A.; DA. 1975; VOL. 72; NO 1; PP. 240-244; BIBL. 21 REF.Article

LA GANGLIOSIDOSE A GM1 (FORME INFANTILE) A PROPOS DE CINQ OBSERVATIONSLARBRE F; CHAZALETTE JP; GUIBAUD P et al.1973; LYON MED.,; FR.; DA. 1973; VOL. 229; NO 4; PP. 335-346; ABS. ANGL.; BIBL. 1P.Serial Issue

Presence of glycoproteins containing the polylactosamine structure in brain and liver of GM1 gangliosidosis patients: comparative study between clinical types I and II, using endo-β-galactosidase enzymeBERRA, B; DE GASPERI, R; RAPELLI, S et al.Neurochemical pathology. 1986, Vol 4, Num 2, pp 107-117, issn 0734-600XArticle

THE ABNORMALITIES OF BETA -GALACTOSIDASE IN GM1 GANGLIOSIDOSESKUDOH T.1978; TOHOKU J. EXPER. MED.; JPN; DA. 1978; VOL. 125; NO 1; PP. 93-101; BIBL. 26 REF.Article

QUANTITATION OF THE ENZYMICALLY DEFICIENT CROSS REACTING MATERIAL IN GM1 GANGLIOSIDOSES.BEN YOSEPH Y; BURTON BK; NADLER HL et al.1977; AMER. J. HUM. GENET.; U.S.A.; DA. 1977; VOL. 29; NO 6; PP. 575-580; BIBL. 23 REF.Article

GENETIC HETEROGENEITY IN GM1-GANGLIOSIDOSIS. = HETEROGENEITE GENETIQUE DANS LA GANGLIOSIDE GMLGALJAARD H; HOOGEVEEN A; KEIJZER W et al.1975; NATURE; G.B.; DA. 1975; VOL. 257; NO 5521; PP. 60-62; BIBL. 22 REF.Article

THE GANGLIOSIDOSESVOLK BW; ADACHI M; SCHNECK L et al.1975; HUM. PATHOL.; U.S.A.; DA. 1975; VOL. 6; NO 5; PP. 555-569; BIBL. 3 P.Article

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