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

GM₃ GANGLIOSIDOSIS: A NOVEL HUMAN SPHINGOLIPODYSTROPHYMACLAREN NK; MAX SR; CORNBLATH M et al.1976; PEDIATRICS; U.S.A.; DA. 1976; VOL. 57; NO 1; PP. 106-110; BIBL. 16 REF.Article

DIE GM₁ GANGLIOSIDOSE. EIN VERSUCH ZUR DIFFERENZIERUNG DES TYP 1 VOM TYP II AUF GRUND VON KLINISCHEN, BIOCHEMISCHEN UND MORPHOLOGISCHEN ASPEKTENCHRISTOMANOS HA.1974; FOLIA BIOCHIM. BIOL. GRAECA; GRECE; DA. 1974; VOL. 11; NO 3-4; PP. 70-79; ABS. ANGL.; BIBL. 16 REF.Article

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

Gangliosidosis GM₂ tipo 2 = Gangliosidose GM2 type II = Gangliosidosis GM2 type 2SANCHEZ-CORONA, J; VACA, G; GONZALES-FLORES, S. A et al.Revista de investigacion clinica. 1985, Vol 37, Num 1, pp 43-47, issn 0034-8376Article

Diagnosis of infantile and juvenile forms of G_M2 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

Presence of glycoproteins containing the polylactosamine structure in brain and liver of G_M1 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

Gangliosidoses and the fetal retinaCOGAN, D. G; KUWABARA, T; KOLODNY, E et al.Ophthalmology (Rochester, MN). 1984, Vol 91, Num 5, pp 508-512, issn 0161-6420Article

Juvenile G_M2 gangliosidosis (A^uMB 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

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

G_M1 gangliosidosis (type 1) in a catBARKER, C. G; BLAKEMORE, W. F; DELL, A et al.Biochemical journal (London. 1906). 1986, Vol 235, Num 1, pp 151-158, issn 0006-2936Article

ENZYME HISTOCHEMICAL AND ULTRASTRUCTURAL ALTERATIONS IN THE BRAINS OF FRIESIAN CALVES WITH GM₁ GANGLIOSIDOSIS = ALTERATIONS ENZYMATIQUES HISTOCHIMIQUES ET DE L'ULTRASTRUCTURE DES CERVEAUX DE VEAUX FRIESIANS, PORTEURS D'UNE GANGLIOSIDOSE GM₁SHEAHAN BJ; DONNELLY WJC.1974; ACTA NEUROPATHOL.; ALLEM.; DA. 1974; VOL. 30; NO 1; PP. 73-84; BIBL. 1 P.Article

Etude de l'hétérogénéité génétique des gangliosidoses humainsAKHUNOV, V. S; ARONOVITCH, E. L; KRASNOPOLSKAYA, K. D et al.Genetika. 1989, Vol 25, Num 10, pp 1861-1871, issn 0016-6758Article

A colorimetric bead-binding assay for detection of intermolecular interactionsIRVINE, A. D; SUN, P; KOS, L et al.Experimental dermatology. 2002, Vol 11, Num 5, pp 462-467, issn 0906-6705, 6 p.Article

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

DIE LUNGENERKRANKUNG BEI GENERALISIERTER GM₁ GANGLIOSIDOSE = L'ATTEINTE PULMONAIRE DANS LA GM₁ GANGLIOSIDOSEHEYNE K; VON DER LINDE J; TRUEBSBACH A et al.1972; HELV. PAEDIATR. ACTA; SUISSE; DA. 1972; VOL. 27; NO 6; PP. 591-600; ABS. ANGL.; BIBL. 21REF.Serial Issue

DIFFERENTIATION OF TWO VARIANTS OF TYPE-AB G_M2 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

A NEW VARIANT OF TYPE-AB GM2-GANGLIOSIDOSISSU CHEN LI; HIRABAYASHI Y; YU TEH LI et al.1981; BIOCHEM. BIOPHYS. RES. COMMUN.; ISSN 0006-291X; USA; DA. 1981; VOL. 101; NO 2; PP. 479-485; BIBL. 13 REF.Article

DONNEES ACTUELLES CONCERNANT LA GANGLIOSIDOSE A GM 1, TYPE 2. A PROPOS D'UN CASRICHARD A.1974; LYON; ASSOC. CORP. ETUD. MED.; DA. 1974; PP. (118P.); BIBL. 22P.1/2; (THESE DOC. MED., CLAUDE-BERNARD LYON)Thesis

Motor neuron disease and adult hexosaminidase A deficiency in two families: evidence for multisystem degenerationMITSUMOTO, H; SLIMAN, R. J; SCHAFER, I. A et al.Annals of neurology. 1985, Vol 17, Num 4, pp 378-385, issn 0364-5134Article

Prenatal diagnosis of G_M2 gangliosidosis with high residual hexosaminidase A activity (variant B¹; pseudo AB variant)CONZELMANN, E; NEHRKORN, H; KYTZIA, H.-J et al.Pediatric research. 1985, Vol 19, Num 11, pp 1220-1224, issn 0031-3998Article

A SENSITIVE METHOD FOR THE DETECTION OF G_M1-GANGLIOSIDE IN RAT ADIPOCYTE PREPARATIONS BASED ON ITS INTERACTION WITH CHOLERAGENPACUSZKA T; MOSS J; FISHMAN PH et al.1978; J. BIOL. CHEM.; USA; DA. 1978; VOL. 253; NO 14; PP. 5103-5108; BIBL. 30 REF.Article