Author:
Marinou Kyriakoula,Tsakiris Stylianos,Tsopanakis Christi,Schulpis Kleopatra H.,Behrakis Panagiotis
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Neurology (clinical),Biochemistry
Reference30 articles.
1. Berry, G.T., and Segal, S. (2000), Disorders of galactose metabolism. In (C.R. Scriver, A.L. Beadet, W.S. Sly, and D. Valle, eds.), The Metabolic and Molecular Basis of Inherited Disorders, McGraw Hill, New York, pp. 1553–1589.
2. Berry, G.T., Leslie, N., Reynolds, R., Yaken, C., and Segal, S. (2001). Evidence for alternative galactose oxidation in a patient with detection of the galactose-1-phosphate uridyltransferase gene. Mol. Gen. Metab. 72:316–321.
3. Berry, G.T., Nissim, I., Lin, Z., Mazur, A.T., Gibson, J.B., and Segal, S. (1995). Evidence for endogenous synthesis of galactose in normal man and patients with galactosaemia. Lancet 346:1073–1074.
4. Bogdanski, D.F., Tissuri, A., and Brodie, B.B. (1968), Role of sodium, potassium, ouebain and reserpine in uptake, storage and metabolism of biogenic amines in synaptosomes. Life Sci. 7:419–428.
5. Bosch, A.M., Bakker, A.H., Van Genni, P., Vankempen, J.V., Wanders, R.J.A., and Wuburg, A. (2003). Clinical features of galactokinase deficiency. A review of the literature. J. Inherit. Metab. 25:629–634.
Cited by
2 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献