History




Garrod, A.E.: Inborn errors of metabolism. Hodder and Stoughton, London (1909)


Hüttl, S., Markovic, O., Siťaj, Š.: Hemarthrosis in ochronotic arthropathy. Z. Rheumaforsch. 25, 169–181 (1966)PubMed


La Du, B.N., Zannoni, V.G., Laster, L., Seegmiller, J.E.: The nature of the defect in tyrosine metabolism in Alkaptonuria. J. Biol. Chem. 230, 251–260 (1958)


Phornphutkul, C., Introne, W.J., Perry, M.B., Bernardini, I., Murphey, M.D., Fitzpatrick, D.L., Anderson, P.D., Huizing, M., Anikster, Y., Gerber, L.H., Gahl, W.A.: Natural history of alkaptonuria. N. Engl. J. Med. 26, 2111–2121 (2002)CrossRef


Pollak, M.R., Chou, Y.H., Cerda, J.J., Steinmann, B., La Du, B.N., Seidman, J.G., Seidman, C.E.: Homozygosity mapping of the gene for alkaptonuria to chromosome 3q2. Nat. Genet. 5, 201–204 (1993)CrossRefPubMed


Rovenský, J., Urbánek, T.: Alkaptonuria and ochronosis. (in Slovak) Lek Obzor. 49, 341–346 (2000)


Rovensky, J., Urbanek, T.: Alkaptonurie a ochronoza. In: Hrncir, Z. (ed.) Klinická revmatologie, pp. 509–516. Galen, Praha (2003)

Oct 14, 2016 | Posted by in RHEUMATOLOGY | Comments Off on History

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