Tyrosinosis (inborn hepato-renal dysfunction).

作者: L I Woolf

DOI: 10.1177/003591576605900903

关键词:

摘要:

参考文章(12)
Hazel R. Bloxam, M. G. Day, Nancy K. Gibbs, L. I. Woolf, An inborn defect in the metabolism of tyrosine in infants on a normal diet Biochemical Journal. ,vol. 77, pp. 320- 326 ,(1960) , 10.1042/BJ0770320
L.I. Woolf, INHERITED METABOLIC DISORDERS: ERRORS OF PHENYLALANINE AND TYROSINE METABOLISM. Advances in Clinical Chemistry. ,vol. 6, pp. 97- 230 ,(1963) , 10.1016/S0065-2423(08)60239-5
L.I. Woolf, Inherited Metabolic Disorders: Galactosemia Advances in Clinical Chemistry. ,vol. 5, pp. 1- 68 ,(1963) , 10.1016/S0065-2423(08)60071-2
S. Halvorsen, L. R. Gjessing, STUDIES ON TYROSINOSIS: 1, EFFECT OF LOW-TYROSINE AND LOW-PHENYLALANINE DIET. BMJ. ,vol. 2, pp. 1171- 1173 ,(1964) , 10.1136/BMJ.2.5418.1171
L. I. Woolf, Renal tubular dysfunction The American Journal of the Medical Sciences. ,vol. 252, pp. 497- ,(1966) , 10.1097/00000441-196610000-00019
STIG FRITZELL, O. RUDOLF JAGENBURG, LARS-BERTIL SCHNÜRER, FAMILIAL CIRRHOSIS OF THE LIVER, RENAL TUBULAR DEFECTS WITH RICKETS AND IMPAIRED TYROSINE METABOLISM. Acta Paediatrica. ,vol. 53, pp. 18- 32 ,(1964) , 10.1111/J.1651-2227.1964.TB07202.X
Colin J, Gentil C, Le Tan Vinh, Roux M, Gabilan Jc, Lelong M, Alagille D, [Congenital and familial cirrhosis, vitamin-resistant rickets with gluco-phosphoamine diabetes, terminal hepatoma]. Pediatrie. ,vol. 16, pp. 221- 229 ,(1961)