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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

GM1 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

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

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

URINARY OLIGOSACCHARIDES OF GMI-GANGLIOSIDOSIS: STRUCTURES OF OLIGOSACCHARIDES EXCRETED IN THE URINE OF TYPE 1 BUT NOT IN THE URINE OF TYPE 2 PATIENTSOHKURA T; YAMASHITA K; KOBATA A et al.1981; J. BIOL. CHEM.; ISSN 0021-9258; USA; DA. 1981; VOL. 256; NO 16; PP. 8485-8490; BIBL. 26 REF.Article

Adult GM1-gangliosidosis: clinical patterns and rectal biopsyNAKANO, T; IKEDA, S.-I; KONDO, K et al.Neurology. 1985, Vol 35, Num 6, pp 875-880, issn 0028-3878Article

Cardiomyopathy and skeletal myopathy in unusual variant of GM1 gangliosidosisCHARROW, J; HVIZD, M. G.The Journal of pediatrics. 1986, Vol 108, Num 5, pp 729-732, issn 0022-3476, 1Article

Preparation and specificity of 11 monoclonal antibodies to GM1 gangliosideMAHADIK, S. P; LAEV, H; RAPPORT, M. M et al.Journal of neurochemistry. 1986, Vol 47, Num 4, pp 1172-1175, issn 0022-3042Article

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

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

GM2 gangliosidosis in a Japanese spanielCUMMINGS, J. F; WOOD, P. A; WALKLEY, S. U et al.Acta neuropathologica. 1985, Vol 67, Num 3-4, pp 247-253, issn 0001-6322Article

A SENSITIVE METHOD FOR THE DETECTION OF GM1-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

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

FINE STRUCTURE OF CUTANEOUS NERVES IN GANGLIOSIDE STORAGE DISEASE.DOLMAN CL; MACLEOD PM; CHANG E et al.1977; J. NEUROL. NEUROSURG. PSYCHIATRY; G.B.; DA. 1977; VOL. 40; NO 6; PP. 588-594; BIBL. 10 REF.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

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

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

Demonstration of GM1-ganglioside in nervous system in generalized GM1-gangliosidosis using cholera toxin B subunitIWAMASA, T; OHSHITA, T; NASHIRO, K et al.Acta neuropathologica. 1987, Vol 73, Num 4, pp 357-360, issn 0001-6322Article

Histochemistry of lipid storage diseasesZUGIBE, F. T.American journal of medical genetics. Supplement. 1987, Num 3, pp 221-226, issn 1040-3787Article

Molecular heterogeneity in the infantile and juvenile forms of Sandhoff disease (O-variant GM2 gangliosidosis)O'DOWD, B. F; KLAVINS, M. H; WILLARD, H. F et al.The Journal of biological chemistry (Print). 1986, Vol 261, Num 27, pp 12680-12685, issn 0021-9258Article

Attenuation of ganglioside GM1 accumulation in the brain of GM1 gangliosidosis mice by neonatal intravenous gene transferTAKAURA, N; YAGI, T; MAEDA, M et al.Gene therapy (Basingstoke). 2003, Vol 10, Num 17, pp 1487-1493, issn 0969-7128, 7 p.Article

Multiple-dose pharmacokinetics of ganglioside GM1 intravenous and intramuscular administration to healthy volunteersROST, K. L; BROCKMOLLER, J; WEBER, W et al.Clinical pharmacology and therapeutics. 1991, Vol 50, Num 2, pp 141-149, issn 0009-9236Article

Tumor necrosis factor enhances GD3 ganglioside expression in cultured human melanocytesFURUKAWA, K; ARITA, Y; SATOMI, N et al.Archives of biochemistry and biophysics (Print). 1990, Vol 281, Num 1, pp 70-75, issn 0003-9861, 6 p.Article

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