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Results 1 to 25 of 12851

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Hepatocellular transplantation in rats with congenital ascorbic acid deficiencyONODERA, K; KASAI, S; MITO, M et al.Nippon Geka Gakkai Zasshi. 1995, Vol 96, Num 5, pp 301-308, issn 0301-4894Article

Effects of Cl channel blockers on Ca-activated chloride and potassium currents in smooth muscle cells from rabbit portal veinHOGG, R. C; WANG, Q; LARGE, W. A et al.British journal of pharmacology. 1994, Vol 111, Num 4, pp 1333-1341, issn 0007-1188Article

Relative efficiency of incorporation of newly synthesized elastin and collagen into aorta, pulmonary artery and pulmonary vein of growing pigsJOHNSON, D. J; LABOURENE, J; RABINOVITCH, M et al.Connective tissue research (Print). 1993, Vol 29, Num 3, pp 213-221, issn 0300-8207Conference Paper

Fabry's disease with complete atrioventricular block : histological evidence of involvement of the conduction systemIKARI, Y; KUWAKO, K; YAMAGUCHI, T et al.British heart journal. 1992, Vol 68, Num 3, pp 323-325, issn 0007-0769Article

Hyperuricemia in medium-chain acyl-coenzyme A dehydrogenase deficiencyDAVIDSON-MUNDT, A; LUDER, A. S; GREENE, C. L et al.The Journal of pediatrics. 1992, Vol 120, Num 3, pp 444-446, issn 0022-3476Article

DNA ploidy abnormalities in the liver of children with hereditary tyrosinemia type I : correlation with histopathologic featuresZERBINI, C; WEINBERG, D. S; HOLLISTER, K. A et al.The American journal of pathology. 1992, Vol 140, Num 5, pp 1111-1119, issn 0002-9440Article

Arachidonic acid- and acetylcholine-induced relaxations of rabbit aortaPFISTER, S. L; CAMPBELL, W. B.Hypertension (Dallas, Tex. 1979). 1992, Vol 20, Num 5, pp 682-689, issn 0194-911XArticle

Pertussis toxin reduces endothelium-dependent and idependent responses to alpha-2 adrenergic stimulation in systemic canine arteries and veinsMILLER, V. M; FLAVAHAN, N. A; VANHOUTTE, P. M et al.The Journal of pharmacology and experimental therapeutics. 1991, Vol 257, Num 1, pp 290-293, issn 0022-3565, 4 p.Article

Clinical presentation and natural course of the carbohydrate-deficient glycoprotein syndromeJAEKEN, J; HAGBERG, B; STRØMME, P et al.Acta paediatrica Scandinavica. Supplement. 1991, Num 375, pp 6-13, issn 0300-8843Conference Paper

Conférences/Journée scientifique sur «Les maladies héréditaires du métabolisme. Du dépistage à la biologie moléculaire», Paris, 13 novembre 1987 = Conferences/Inborn errors of metabolism. From screening to molecular biology scientific meeting. Paris, November 13, 1987Annales de biologie clinique (Paris). 1988, Vol 46, Num 6, pp 381-405, issn 0003-3898Conference Proceedings

Epoxy acids in peroxisomal disordersSTOKKE, O; JELLUM, E; KVITTINGEN, E. A et al.Scandinavian journal of clinical & laboratory investigation. 1986, Vol 46, Num 1, pp 95-96, issn 0036-5513Article

Heritable metabolic storage diseasesGEBHART, W.Journal of cutaneous pathology. 1985, Vol 12, Num 3-4, pp 348-357, issn 0303-6987Article

Blood cells as markers for metabolic disordersBEUTLER, E.Blut. 1985, Vol 51, Num 6, pp 371-376, issn 0006-5242Article

Metabolische Myopathien im Kindesalter i eine Übersicht in kurzgefasster Form = Myopathies métaboliques chez le nourrisson et l'enfant: brève revue = Metabolic myopathies in infancy and childhood. A concise reviewSCHAUB, J.Monatsschrift für Kinderheilkunde. 1984, Vol 132, Num 8, pp 566-573, issn 0026-9298Article

Metabolische Myopathien = Myopathies métaboliques = Metabolic myopathiLÖSSNER, J; KÜHN, H. J.Psychiatrie, Neurologie und medizinische Psychologie. 1984, Vol 36, Num 9, pp 513-526, issn 0033-2739Article

Follow-up study of a nation-wide neonatal metabolic screening program in Japan: a collaborative study group of neonatal screening for inborn enor of metabolism in japanTADA, K; TATEDA, H; KURODA, Y et al.European journal of pediatrics. 1984, Vol 142, Num 3, pp 204-207, issn 0340-6199Article

Screeninggutersuchungen auf angeborene Stoffwechselerkrankungen bei geistig retardieren Patienten in 6 psychiatrischen Anstalten Niedersachsens = Dépistage des troubles métaboliques congénitaux chez des retardés mentaux dans 6 institutions psychiatriques de Basse Sabe = Congenital metabolic disorders screening in mental retarded patients of six lower Saxony psychiatric institutionsBYRD, D. J; BRÖTLING, D; BRODEHL, J et al.Klinische Pädiatrie. 1984, Vol 196, Num 5, pp 298-303, issn 0300-8630Article

Familial systemic carnitine deficiencyCRUSE, R. P; DI MAURO, S; TOWFIGHI, J et al.Archives of neurology (Chicago). 1984, Vol 41, Num 3, pp 301-305, issn 0003-9942Article

Historical outline of the biological importance of trace metalsWILLIAMS, D. R.Journal of inherited metabolic disease. 1983, Vol 6, pp 1-4, issn 0141-8955, suppl. 1Article

Abstracts/2nd International symposium [on] monoclonal antibodies and inborn errors of metabolism, Brugge, October 20-22, 1983International symposium on monoclonal antibodies and inborn errors of metabolism. 2. 1983, 116 p.Conference Proceedings

Expression of nitric oxide synthase by cytokines in vascular smooth muscle cellsKOIDE, M; KAWAHARA, Y; TSUDA, T et al.Hypertension (Dallas, Tex. 1979). 1994, Vol 23, Num 1, pp 45-48, issn 0194-911X, SUPConference Paper

Association of Fabry's disease with femoral head avascular necrosis. Editorial commentROSS, G; KUWAMURA, F; GORAL, A et al.Orthopedics (Thorofare). 1993, Vol 16, Num 4, pp 471-473, issn 0147-7447Article

Isolated vitamin E deficiency and progressive ataxiaRAYNER, R. J; DORAN, R; ROUSSOUNIS, S. H et al.Archives of disease in childhood. 1993, Vol 69, Num 5, pp 602-603, issn 0003-9888Article

Are arterial pressure and deformation the sole determinants of baroreceptor activity ? Importance of humoral and endothelial modulation in normal and disease statesCHAPLEAU, M. W.Hypertension (Dallas, Tex. 1979). 1992, Vol 19, Num 3, pp 278-280, issn 0194-911XArticle

Gaucher's disease in an infant diagnosed by fine needle aspiration of the liver and spleen : a case reportDOMANSKI, H; DEJMEK, A; LJUNG, R et al.Acta cytologica. 1992, Vol 36, Num 3, pp 410-412, issn 0001-5547Article

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