Pellagra with colitis due to a defect in tryptophan metabolism

Author:

Clayton P. T.,Bridges N. A.,Atherton D. J.,Milla P. J.,Malone M.,Bender D. A.

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Reference15 articles.

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2. Fenton DA, Wilkinson JD, Toseland PA (1983) Family exhibiting cerebellar-like ataxia, photosensitivity and shortness of stature — a new inborn error of tryptophan metabolism. J R Soc Med 76:736–739

3. Freundlich E, Statter M, Yatziv S (1981) Familial pellagra-like skin rash with neurological manifestations. Arch Dis Child 56:146–148

4. Joseph MH, Lofthouse R (1987) The preservation of whole blood serotonin and its determination using HPLC. In: Bender DA, Joseph MH, Kochen W, Steinhart H (eds) Progress in tryptophan and serotonin research. Walter de Gruyter, Berlin, pp 385–388

5. Komrower GM, Westall R (1967) Hydroxykynureninuria. Am J Dis Child 113:73–80

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