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kw.\*:("Esfingolipidosis hereditaria Gaucher")

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β-glucosidases: bases moléculaires de la maladie de Gaucher = B-glucosidases. Molecular bases of Gaucher diseaseMARET, A; SALVAYRE, R; NEGRE, A et al.Transactions of the Zoological Society of London. 1985, Vol 33, Num 6, pp 693-713, issn 0084-5620Article

Gaucher's disease: advances and challengesMARTIN, B. M; SIDRANSKY, E; GINNS, E. I et al.Advances in pediatrics. 1989, Vol 36, pp 277-306, issn 0065-3101, 30 p.Article

Sodium taurocholate effect on β-glucosidase activity: a new approach for identification of Gaucher disease using the synthetic substrate and leucocytesMAGALHAES, J; SA MIRANDA, M. C; PINTO, R et al.Clinica chimica acta. 1984, Vol 141, Num 2-3, pp 111-118, issn 0009-8981Article

Gaucher's disease affecting the mandibleHALL, M. B; BROWN, R. W; BAUGHMAN, R. A et al.Journal of oral and maxillofacial surgery. 1985, Vol 43, Num 3, pp 210-213, issn 0278-2391Article

Molecular weight characterization of β-glucocerebrosidase in mononuclear white blood cells in Gaucher's diseasePIRRUCCELLO, S; BARRANGER, J. A; BARTON, N. W et al.Biochemical medicine. 1984, Vol 31, Num 1, pp 73-79, issn 0006-2944Article

Complex alleles of the acid β-glucosidase gene in Gaucher diseaseLATHAM, T; GRABOWSKI, G. A; THEOPHILUS, B. D. M et al.American journal of human genetics. 1990, Vol 47, Num 1, pp 79-86, issn 0002-9297, 8 p.Article

La participation rétinienne dans la maladie de Gaucher = Retinal involvement in Gaucher's diseaseGONZALEZ RODRIGUEZ, M. J; PINTADO CONDE, H; LOPEZ NIETO, C et al.Journal français d'ophtalmologie. 1992, Vol 15, Num 3, pp 185-190, issn 0181-5512Article

Successful treatment of bone marrow failure in Gaucher's disease with low-dose modified glucocerebrosidaseMISTRY, P. K; DAVIES, D; CORFIELD, A et al.Quarterly journal of medicine. 1992, Vol 83, Num 303, pp 541-546, issn 0033-5622Article

La splénectomie dans la maladie de gaucher. A propos de deux cas dont l'un précédé d'une embolisation = Splenectomy in Gaucher's disease. Report of two cases, one of which was preceded by embolisationSAMAMA, G; BREFORT, J. L; DOLLEY, M et al.Annales de chirurgie (Paris). 1989, Vol 43, Num 5, pp 367-370, issn 0003-3944, 4 p.Article

Scintigraphic findings in Gaucher's diseaseISRAEL, O; JERUSHALMI, J; FRONT, D et al.Journal of nuclear medicine. 1986, Vol 27, Num 10, pp 1557-1563, issn 0097-9058Article

Direct evidence by carbon-13 NMR spectroscopy for the erythro configuration of the sphingoid moiety in Gaucher cerebroside and other natural sphingolipidsSARMIENTOS, F; SCHWARZMANN, G; SANDHOFF, K et al.European journal of biochemistry (Print). 1985, Vol 146, Num 1, pp 59-64, issn 0014-2956Article

Neurological involvement in type 1 (adult) Gaucher's diseaseMCKERAN, R. O; BRADBURY, P; TAYLOR, D et al.Journal of neurology, neurosurgery and psychiatry. 1985, Vol 48, Num 2, pp 172-175, issn 0022-3050Article

High level transcription of the glucocerebrosidase pseudogene in normal subjects and patients with Gaucher diseaseSORGE, J; GROSS, E; WEST, C et al.The Journal of clinical investigation. 1990, Vol 86, Num 4, pp 1137-1141, issn 0021-9738Article

A mutation in the human glucocerebrosidase gene in neuronopathic Gaucher's diseaseTSUJI, S; CHOUDARY, P. V; MARTIN, B. M et al.The New England journal of medicine. 1987, Vol 316, Num 10, pp 570-575, issn 0028-4793Article

The varied clinical and laboratory manifestations of type II Gaucher's diseaseLAKS, Y; PASSWELL, J.Acta paediatrica scandinavica. 1987, Vol 76, Num 2, pp 378-380, issn 0001-656XArticle

Activators of spleen glucocerebrosidase from controls and patients with various forms of Gaucher's diseaseBASU, A; GLEW, R. H; DANIELS, L. B et al.The Journal of biological chemistry (Print). 1984, Vol 259, Num 3, pp 1714-1719, issn 0021-9258Article

Complementation analysis in Gaucher disease using single cell microassay techniques. Evidence for a single Gaucher genëGRAVEL, R. A; LEUNG, A.Human genetics. 1983, Vol 65, Num 2, pp 112-116, issn 0340-6717Article

Antibody response in patients with Gaucher disease after repeated infusion with macrophage-targeted glucocerebrosidaseRICHARDS, S. M; OLSON, T. A; MCPHERSON, J et al.Blood. 1993, Vol 82, Num 5, pp 1402-1409, issn 0006-4971Article

Role of pH in determining the cell-type-specific residual activity of glucocerebrosidase in type 1 Gaucher diseaseVAN WEELY, S; VAN DEN BERG, M; BARRANGER, J. A et al.The Journal of clinical investigation. 1993, Vol 91, Num 3, pp 1167-1175, issn 0021-9738Article

Home treatment with intravenous enzyme replacement therapy for Gaucher disease : an international collaborative study of 33 patientsZIMRAN, A; HOLLAK, C. E. M; ABRAHAMOV, A et al.Blood. 1993, Vol 82, Num 4, pp 1107-1109, issn 0006-4971Article

Mutations in Jewish patients with Gaucher diseaseBEUTLER, E; GELBART, T; KUHL, W et al.Blood. 1992, Vol 79, Num 7, pp 1662-1666, issn 0006-4971Article

Maladie de Gaucher et grossesse = Gaucher's disease and pregnancyTORDJEMAN, N; MONNIER, J. C; HAUTFEUILLE, P et al.Journal de gynécologie obstétrique et biologie de la reproduction. 1991, Vol 20, Num 6, pp 835-840, issn 0368-2315Article

Neurologic complications of nonneuronopathic Gaucher's diseaseGREWAL, R. P; DOPPELT, S. H; THOMPSON, M. A et al.Archives of neurology (Chicago). 1991, Vol 48, Num 12, pp 1271-1272, issn 0003-9942Article

Activity of glucocerebrosidase in extracts of different cell types from type 1 Gaucher disease patientsSA MIRANDA, M. C; AERTS, J. M. F. G; PINTO, R et al.Clinical genetics. 1990, Vol 38, Num 3, pp 218-227, issn 0009-9163Article

Abnormalities in lipoprotein metabolism in Gaucher type 1 diseaseNGOC ANH LE; GIBSON, J. C; RUBINSTEIN, A et al.Metabolism, clinical and experimental. 1988, Vol 37, Num 3, pp 240-245, issn 0026-0495Article

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