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Treatment of Two Children with Hereditary Tyrosinaemia Type I and Long-standing Renal Disease with a 4-hydroxyphenylpyruvate Dioxygenase Inhibitor (NTBC)

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Publisher Wiley
Date 1996 Jan 1
PMID 8739974
Citations 5
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References
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Shoemaker L, Strife C, Balistreri W, Ryckman F . Rapid improvement in the renal tubular dysfunction associated with tyrosinemia following hepatic replacement. Pediatrics. 1992; 89(2):251-5. View

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Lindstedt S, Holme E, Lock E, Hjalmarson O, Strandvik B . Treatment of hereditary tyrosinaemia type I by inhibition of 4-hydroxyphenylpyruvate dioxygenase. Lancet. 1992; 340(8823):813-7. DOI: 10.1016/0140-6736(92)92685-9. View

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van Spronsen F, Thomasse Y, Smit G, Leonard J, Clayton P, Fidler V . Hereditary tyrosinemia type I: a new clinical classification with difference in prognosis on dietary treatment. Hepatology. 1994; 20(5):1187-91. View