1 |
Archibald EG. The incidence of alkaptonuria : A study in chemical individuality. Lancet 1902;13:1616-20
|
2 |
Karl SR. Alkaptonuria. Emedicine.com Available from : http://www.emedicine.com/ped/topic64.htm : July 2, 2005
|
3 |
Sarkany RP, Breathnach SM, Seymour CA, Weismann K, Burns DA. Metabolic and nutritional disorders. Textbook of Dermatology. 7th ed. Oxford : Blackwell Science 2004;3:81-3
|
4 |
Soker CS, Cevik R, Aksunger A, Unlu K, Ava S. Ocular ochronosis : A case report and clinical findings. Acta Ophthalmol Scand 2002;80:340-2
DOI
ScienceOn
|
5 |
Richard EB, Robert MK, Hal BJ. Nelson textbook of pediatrics. 17th ed. : Saunders 2004:403-4
|
6 |
Lubics A, Schneider I, Sebok B, Havass Z. Extensive bluish gray skin pigmentation and severe arthropathy. Endogenous ochronosis. Arch Derma 2000;33:239-48
|
7 |
Goldsmith L. Disorders of metabolism. Dermatology in General Medicine. 3rd ed. New York : McGraw-Hill Book Co, 1987;1642-6.
|
8 |
Haas V, Carbasius EC, Klerk JB, Bakker HD, Smit GP, Huijbers WA, et al. The success of dietary protein restriction in alkaptonuria patients is age-dependent. J Inherit Metab Dis 1998;21:791-8
DOI
ScienceOn
|
9 |
Seegmiller JE. An enzymatic spectrophotometric method for the determination of homogentisic acid in the plasma and urine. J Biol Chem 1961;236:774-7
|