Diagnosis and treatment of tyrosinosis.

Author:

Fairney A.,Francis D.,Ersser R. S.,Seakins J. W.,Cottom D.

Publisher

BMJ

Subject

Pediatrics, Perinatology and Child Health

Reference22 articles.

1. Clinical effects of low-tyrosine low-phenylalanine diet in a case of tyrosinemia;Aronsson, S.; Englesson, G.; Jagenburg, R.; Palmgren, B.,1966

2. Transient tyrosinemia of the newborn: dietary and clinical aspects;Avery, M.E.; Clow, C.L.; Menkes, J.H.; Ramos, A.; Scriver, C.R.; Stern, L.; Wasserman, B.P.;Pediatrics,1967

3. An inborn defect in the metabolism of tyrosine in infants on a normal diet;Bloxam, H.R.; Day, M.G.; Gibbs, N.K.; Woolf, L.I.;Biochem. J7,1960

4. Biochemical and EEG studies in phenylketonuric children during phenylalanine tolerance tests;Clayton, B.E.; Moncrieff, A.A.; Pampiglione, G.; Shepherd, J.;Arch. Dis. Childh,1966

5. Dietary treatment in tyrosinemia (tyrosinosis);Gentz, J.; Lindblad, B.; Lindstedt, S.; Levy, L.; Shasteen, W.; Zetterstrom, R.;Amer. J. Dis. Child,1967

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1. N ‐acetyl‐ l ‐tyrosine is an intrinsic triggering factor of mitohormesis in stressed animals;EMBO reports;2020-03-02

2. Pediatric Fanconi Syndrome;Pediatric Nephrology;2015-11-12

3. Pediatric Fanconi Syndrome;Pediatric Nephrology;2014

4. Fanconi Syndrome;Pediatric Nephrology;2009

5. TYROSINEMIA;Pathology International;1979-07

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