Prospective treatment of cerebrotendinous xanthomatosis with cholic acid therapy
暂无分享,去创建一个
[1] P. Clayton,et al. Disorders of bile acid synthesis , 2006, Journal of Inherited Metabolic Disease.
[2] G. Nandakumar,et al. Cerebrotendinous xanthomatosis: need for early diagnosis. , 2006, Indian journal of dermatology, venereology and leprology.
[3] K. Setchell,et al. Defects in bile acid biosynthesis--diagnosis and treatment. , 2006, Journal of pediatric gastroenterology and nutrition.
[4] W. Walker. Pediatric Gastrointestinal Disease , 2004 .
[5] R. Wevers,et al. Mutations in the sterol 27-hydoxylase gene (CYP27A) cause hepatitis of infancy as well as cerebrotendinous xanthomatosis , 2002, Journal of Inherited Metabolic Disease.
[6] P. Clayton. Applications of mass spectrometry in the study of inborn errors of metabolism , 2001, Journal of Inherited Metabolic Disease.
[7] Lee Kw,et al. Cerebrotendinous xanthomatosis in three siblings from a Chinese family. , 2001 .
[8] K. F. Ko,et al. Cerebrotendinous xanthomatosis in three siblings from a Chinese family. , 2001, Singapore medical journal.
[9] M. A. Croce,et al. Four novel mutations of sterol 27-hydroxylase gene in Italian patients with cerebrotendinous xanthomatosis. , 1997, Journal of lipid research.
[10] Y. Tokimura,et al. Treatment of cerebrotendinous xanthomatosis: effects of chenodeoxycholic acid, pravastatin, and combined use , 1994, Journal of the Neurological Sciences.
[11] G. Tint,et al. Comparative effects of lovastatin and chenodeoxycholic acid on plasma cholestanol levels and abnormal bile acid metabolism in cerebrotendinous xanthomatosis. , 1994, Metabolism: clinical and experimental.
[12] D. Russell,et al. Bile acid biosynthesis. , 1992, Biochemistry.
[13] Y. Matsuzawa,et al. Combined treatment with chenodeoxycholic acid and pravastatin improves plasma cholestanol levels associated with marked regression of tendon xanthomas in cerebrotendinous xanthomatosis. , 1991, Metabolism: clinical and experimental.
[14] Y. Seyama,et al. Cerebrotendinous xanthomatosis: Clinical and biochemical evaluation of eight patients and review of the literature , 1991, Journal of the Neurological Sciences.
[15] H. Jörnvall,et al. Cloning, structure, and expression of the mitochondrial cytochrome P-450 sterol 26-hydroxylase, a bile acid biosynthetic enzyme. , 1989, The Journal of biological chemistry.
[16] J. C. van der Molen,et al. Bile acid therapies applied to patients suffering from cerebrotendinous xanthomatosis. , 1985, Clinica chimica acta; international journal of clinical chemistry.
[17] J. Sjövall,et al. Fast atom bombardment mass spectrometry in the diagnosis of cerebrotendinous xanthomatosis. , 1985, Scandinavian journal of clinical and laboratory investigation.
[18] H. Yasuhara,et al. Membrane effects of various drugs on isolated rat hepatocytes and erythrocytes. , 1985, Toxicology and applied pharmacology.
[19] S. Shefer,et al. Long-term treatment of cerebrotendinous xanthomatosis with chenodeoxycholic acid. , 1984, The New England journal of medicine.
[20] G. Tint,et al. A 25-hydroxylation pathway of cholic acid biosynthesis in man and rat. , 1976, The Journal of clinical investigation.
[21] G. Salen,et al. Chenodeoxycholic acid inhibits increased cholesterol and cholestanol synthesis in patients with cerebrotendinous xanthomatosis. , 1975, Biochemical medicine.
[22] G. Salen. Cholestanol deposition in cerebrotendinous xanthomatosis. A possible mechanism. , 1971, Annals of internal medicine.
[23] P. Swanson,et al. Cerebrotendinous Xanthomatosis: The Storage of Cholestanol Within the Nervous System , 1968 .