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

Type 3 (adult) GM₁ gangliosidosis: case reportOHTA, K; TSUJI, S; MIZUNO, Y et al.Neurology. 1985, Vol 35, Num 10, pp 1490-1494, issn 0028-3878Article

CHARACTERIZATION OF OLIGOSACCHARIDES AND GLYCOPEPTIDES EXCRETED IN THE URINE OF G_M1-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

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 G_M1 GANGLIOSIDOSIS. OCCURRENCE WITH ABSENCE OF TWO BETA -GALACTOSIDASE COMPONENTS = GANGLIOSIDOSE G_M1 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

STRUCTURE OF THE GLYCOPEPTIDE STORAGE MATERIAL IN G_M1 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

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 GM_I (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 GM₁ GANGLIOSIDOSIS: CLINICAL, PATHOLOGICAL, CHEMICAL AND ENZYMATIC STUDIES = GANGLIOSIDOSE GM₁ JUVENILE: ETUDE CLINIQUE, ANATOMO-PATHOLOGIQUE, CHIMIQUE ET ENZYMATIQUEO'BRIEN JS; HO MW; VEATH ML et al.1972; CLIN. GENET.; DANM.; DA. 1972; VOL. 3; NO 6; PP. 411-434; BIBL. 22REF.Serial Issue

GM₁ gangliosidosis: clinical and laboratory findings in eight familiesGIUGLIANI, R; COELHO DUTRA, J; SARAIVA PEREIRA, M. L et al.Human genetics. 1985, Vol 70, Num 4, pp 347-354, issn 0340-6717Article

Failure of plasma membranes of astrocytes in primary culture to insert exogenous ganglioside GM1ASOU, H; BRUNNGRABER, E. G.Neuroscience letters. 1984, Vol 46, Num 1, pp 115-118, issn 0304-3940Article

abnormalities of cerebral lipids in GM1-gangliosidoses, infantile, juvenile, and chronic typeKASAMA, T; TAKETOMI, T.Japanese journal of experimental medicine. 1986, Vol 56, Num 1, pp 1-11, issn 0021-5031Article

THE ABNORMALITIES OF BETA -GALACTOSIDASE IN G_M1 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 G_M1 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 HUMAN PURKINJE CELLS: A GOLGI STUDY IN PATHOLOGYFUJISAWA K; NAKAMURA A.1982; ACTA NEUROPATHOL.; ISSN 0001-6322; DEU; DA. 1982; VOL. 56; NO 4; PP. 255-264; BIBL. 25 REF.Article

GM₁ GANGLIOSIDOSIS: PHENOTYPIC VARIATION IN A SINGLE FAMILYFARRELL DF; OCHS U.1981; ANN. NEUROL.; ISSN 0364-5134; USA; DA. 1981; VOL. 9; NO 3; PP. 225-231; BIBL. 36 REF.Article

ATYPICAL EXPRESSION OF BETA -GALACTOSIDASE DEFICIENCY IN A CHILD WITH HURLER-LIKE FEATURES BUT WITHOUT NEUROLOGICAL ABNORMALITIES.ANDRIA G; DEL GIUDICE E; REUSER AJJ et al.1978; CLIN. GENET.; DNK; DA. 1978; VOL. 14; NO 1; PP. 16-23; BIBL. 2 P.Article

THREE CASES OF G_M1-GANGLIOSIDOSIS.KUDOH T; ORII T; NAKAO T et al.1976; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1976; VOL. 70; NO 2; PP. 277-283; BIBL. 25 REF.Article

THE LIVER IN GM₁ GANGLIOSIDOSIS TYPES1 AND 2. A LIGHT AND ELECTRON MICROSCOPICAL STUDY = LE FOIE DANS LA GANGLIOSIDOSE GM₁ DE TYPES 1 ET 2. ETUDE EN MICROSCOPIE OPTIQUE ET ELECTRONIQUEPETRELLI M; BLAIR JD.1975; ARCH. PATHOL.; U.S.A.; DA. 1975; VOL. 99; NO 2; PP. 111-116; BIBL. 29REF.Article

OLIGOSACCHARIDES ACCUMULATING IN THE LIVER FROM A PATIENT WITH G_M2-GANGLIOSIDOSIS VARIANT O (SANDHOFF-JATZKEWITZ DISEASE)YING KIN NMKN; WOLFE LS.1974; BIOCHEM. BIOPHYS. RES. COMMUNIC.; U.S.A.; DA. 1974; VOL. 59; NO 3; PP. 837-844; BIBL. 14REF.Article

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

DOG GM₁ GANGLIOSIDOSIS: CHARACTERIZATION OF THE RESIDUAL LIVER ACID-BETA -GALACTOSIDASERITTMANN LS; TENNANT LL; O'BRIEN JS et al.1980; AM. J. HUM. GENET.; ISSN 0002-9297; USA; DA. 1980; VOL. 32; NO 6; PP. 880-889; BIBL. 13 REF.Article