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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

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

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

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

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

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

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

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

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

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

The biochemistry of HEXA and HEXB gene mutations causing GM2 gangliosidosisMAHURAN, D. J.Biochimica et biophysica acta. Molecular basis of disease. 1991, Vol 1096, Num 2, pp 87-94Article

GM1 Gangliosidose und dilatative CardiomyopathieSIMMA, B; SPERL, W; HAMMERER, I et al.Klinische Pädiatrie. 1990, Vol 202, Num 3, pp 183-185, issn 0300-8630Article

Biochemical basis of type AB GM2 gangliosidosis in a Japanese SpanielISHIKAWA, Y; SU-CHEN LI; WOOD, P. A et al.Journal of neurochemistry. 1987, Vol 48, Num 3, pp 860-864, issn 0022-3042Article

Immunoelectron microscopical localization of lysosomal β-galactosidase and its precursor forms in normal and mutant human fibroblastsWILLEMSEN, R; HOOGEVEEN, A. T; SIPS, H. J et al.European journal of cell biology. 1986, Vol 40, Num 1, pp 9-15, issn 0171-9335Article

The effects of glycolipids and carbohydrates on bilirubin cytotoxicity in vitroSUGITA, K; SATO, T; FUSE, A et al.Biology of the neonate. 1986, Vol 49, Num 5, pp 255-260, issn 0006-3126Article

Proceedings/Joint CNRS-INSERM international symposium and NATO Advanced Research Workshop on enzymes of lipid metabolism II, October 14-18, 1985, Strasbourg, FRAFREYSZ, L; DREYFUS, H; MASSARELLI, R et al.NATO ASI series. Series A : life sciences. 1986, Vol 116, issn 0258-1213, XV-853 pConference Proceedings

Characteristics of asparagine-linked sugar chains of sphingolipid activator protein 1 purified from normal human liver and GM1 gangliosidosis (type 1) liverYAMASHITA, K; INUI, K; TOTANI, K et al.Biochemistry (Easton). 1990, Vol 29, Num 12, pp 3030-3039, issn 0006-2960, 10 p.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

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

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