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kw.\*:("Hiperquilomicronemia")

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Results 1 to 25 of 55

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Steatorrhea and disorders of chylomicron synthesis and secretionLEVY, E; CHOURAQUI, J.-P; ROY, C. C et al.The Pediatric clinics of North America. 1988, Vol 35, Num 1, pp 53-67, issn 0031-3955Article

Autoimmune hyperchylomicronemiaKIHARA, S; MATSUZAWA, Y; KUBO, M et al.The New England journal of medicine. 1989, Vol 320, Num 19, pp 1255-1259, issn 0028-4793Article

A missense (Asp250→Asn) mutation in the lipoprotein lipase gene in two unrelated families with familial lipoprotein lipase deficiencyISHIMURA-OKA, K; SEMENKOVICH, C. F; CHAN, L et al.Journal of lipid research. 1992, Vol 33, Num 5, pp 745-754, issn 0022-2275Article

Deficit en lipoproteine lipase. A propos de deux observations = Lipoprotein-lipase deficiency. Two casesGUYOT, A; BOST, N; GROSLAMBERT, P et al.Pédiatrie (Marseille). 1986, Vol 41, Num 1, pp 33-39, issn 0031-4021Article

The familial hyperchylomicronaemia syndromeBIJVOET, S. M; BRUIN, T; KASTELIN, J. J. P et al.Netherlands journal of medicine. 1993, Vol 42, Num 1-2, pp 36-44, issn 0300-2977Conference Paper

Metabolism of plasma low density lipoproteins in familial combined hyperlipidaemia : effect of acipimox therapyERICSSON, S; ERIKSSON, M; BERGLUND, L et al.Journal of internal medicine. 1992, Vol 232, Num 4, pp 313-320, issn 0954-6820Article

Les déficits en lipoprotéine lipase = Lipoprotein lipase deficienciesETIENNE, J; BRAULT, D.Annales de biologie clinique (Paris). 1992, Vol 50, Num 5, pp 299-309, issn 0003-3898Article

A mutation in the human lipoprotein lipase gene as the most common cause of familial chylomicronemia in French CanadiansYUANHONG MA; HENDERSON, H. E; DAVIGNON, J et al.The New England journal of medicine. 1991, Vol 324, Num 25, pp 1761-1766, issn 0028-4793, 6 p.Article

Hyperchylomicronémie familiale associée à un diabète insulino dépendant : A propos d'une observation = Familial hyperchylomicronemia associated with diabetes : About one caseZOUARI, N; LAHOUAL, N; HASSAYOUN, S et al.Revue maghrébine de pédiatrie. 2004, Vol 14, Num 4, pp 203-206, issn 0330-7611, 4 p.Article

Hyperchylomicronémie familiale avec nouvelle mutation du gène de la lipoprotéine lipase = Familial hyperchylomicronemia with a novel lipoprotein lipase gene mutationCAUSERET, A.-S; SOUILLET, A.-L; MARCAIS, C et al.Annales de dermatologie et de vénéréologie. 2001, Vol 128, Num 12, pp 1343-1345, issn 0151-9638Article

Identification of compound heterozygous mutations (G188E/W382X) of lipoprotein lipase gene in a Japanese infant with hyperchylomicronemia : The G188E mutation was newly identified in JapaneseTAKAGI, A; IKEDA, Y; TACHI, K et al.Clinica chimica acta. 1999, Vol 285, Num 1-2, pp 143-154, issn 0009-8981Article

Characterization of a new case of autoimmune type I hyperlipidemia : Long-term remission under immunosuppressive therapyPRUNETA, V; MOULIN, P; LABROUSSE, F et al.The Journal of clinical endocrinology and metabolism. 1997, Vol 82, Num 3, pp 791-796, issn 0021-972XArticle

Complete paternal isodisomy for chromosome 8 unmasked by lipoprotein lipase deficiencyBENLIAN, P; FOUBERT, L; GAGNE, E et al.American journal of human genetics. 1996, Vol 59, Num 2, pp 431-436, issn 0002-9297Article

Comparison of the hypolipidemic effect of gemfibrozil versus simvastatin in patients with type III hyperlipoproteinemiaCIVEIRA, F; CENARRO, A; FERRANDO, J et al.The American heart journal. 1999, Vol 138, Num 1, pp 156-162, issn 0002-8703, 1Article

A new mutation in the human lipoprotein lipase gene causing familial hyperchylomicronaemiaANWAR, R; PUNTIS, J. W. L; MARKHAM, A. F et al.MP. Molecular pathology. 1997, Vol 50, Num 4, pp 221-223, issn 1366-8714Article

A new case of apo C-II deficiency with a nonsense mutation in the apo C-II geneZANELLI, T; CATAPANO, A. L; AVERNA, M. R et al.Clinica chimica acta. 1994, Vol 224, Num 2, pp 111-118, issn 0009-8981Article

A missense mutation(Trp86→Arg) in exon 3 of the lipoprotein lipase gene : a caus of familial chylomincronemiaISHIMURA-OKA, K; FAUSTINELLA, F; KIHARA, S et al.American journal of human genetics. 1992, Vol 50, Num 6, pp 1275-1280, issn 0002-9297Article

Apolipoprotein C-II deficiency syndrome due to apo C-IIHamburg : clinical and biochemical features and HphI restriction enzyme polymorphismBEIL, F. U; FOJO, S. S; BREWER, H. B et al.European journal of clinical investigation. 1992, Vol 22, Num 2, pp 88-95, issn 0014-2972Article

Genetic epidemiology of lipoprotein lipase deficiency in Saguenay-Lac-St-Jean (Québec, Canada)DIONNE, C; GAGNE, C; JULIEN, P et al.Annales de génétique (Paris). 1992, Vol 35, Num 2, pp 89-92, issn 0003-3995Article

Pancreatitis induced by oestrogen in a patient with type I hyperliproteinaemiaSTUYT, P. M. J; DEMACKER, P. N. M; STALENHOEF, A. F. H et al.British medical journal (1857). 1986, Vol 293, Num 6549, issn 0007-1447, 734Article

Aspect inhabituel du sérum chez un nouveau-né révélant une hyperchylomicronémie à l'origine d'une pancréatite aiguë = Unusual aspect of the serum at a newborn child revealing a hyperchylomicronemia at the origan of an acute pancreatitisDESROYS DU ROURE, F; LETERRIER, M; LE BOTERFF, C et al.Immuno analyse & biologie spécialisée. 2011, Vol 26, Num 1, pp 35-40, issn 0923-2532, 6 p.Article

Reversibility of insulin resistance in obese diabetic patients : role of plasma lipidsMINGRONE, G; DEGAETANO, A; GRECO, A. V et al.Diabetologia (Berlin). 1997, Vol 40, Num 5, pp 599-605, issn 0012-186XArticle

Therapeutic response to medium-chain triglycerides and ω-3 fatty acids in a patient with the familial chylomicronemia syndromeROUIS, M; DUGI, K. A; PREVIATO, L et al.Arteriosclerosis, thrombosis, and vascular biology. 1997, Vol 17, Num 7, pp 1400-1406, issn 1079-5642Article

Heterozygous apolipoprotein C-II deficiency : lipoprotein and apoprotein phenotype and Rsal restriction enzyme polymorphism in the Apo C-IIPadova kindredGABELLI, C; BILATO, C; SANTAMARINA-FOJO, S et al.European journal of clinical investigation. 1993, Vol 23, Num 9, pp 522-528, issn 0014-2972Article

Metabolic abnormalities in hyperlipidemiasMAROTTA, G; PAUCIULLO, P; MANCINI, M et al.Nutrition research (New York, NY). 1993, Vol 13, pp S61-S72, issn 0271-5317, SUP1Conference Paper

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