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Cheminal R, Echenne B, Bellet H, Duran M (1996). "Congenital non-progressive encephalopathy and deafness with intermittent episodes of coma and hyperkynureninuria". Journal of Inherited Metabolic Disease. 19 (1): 25–30. doi:10.1007/BF01799345. PMID8830173. S2CID810814.
Salih MA, Bender DA, McCreanor GM (November 1985). "Lethal familial pellagra-like skin lesion associated with neurologic and developmental impairment and the development of cataracts". Pediatrics. 76 (5): 787–793. doi:10.1542/peds.76.5.787. PMID4058988. S2CID11014655.
Hirata Y, Kawachi T, Sugimura T (October 1967). "Fatty liver induced by injection of L-tryptophan". Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism. 144 (2): 233–241. doi:10.1016/0005-2760(67)90153-1. PMID4168935.
Maes M, Verkerk R, Bonaccorso S, Ombelet W, Bosmans E, Scharpé S (September 2002). "Depressive and anxiety symptoms in the early puerperium are related to increased degradation of tryptophan into kynurenine, a phenomenon which is related to immune activation". Life Sciences. 71 (16): 1837–1848. doi:10.1016/s0024-3205(02)01853-2. PMID12175700.
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Bartoli, F; Misiak, B; Callovini, T; Cavaleri, D; Cioni, RM; Crocamo, C; Savitz, JB; Carrà, G (July 2021). "The kynurenine pathway in bipolar disorder: a meta-analysis on the peripheral blood levels of tryptophan and related metabolites". Molecular Psychiatry. 26 (7): 3419–3429. doi:10.1038/s41380-020-00913-1. PMID33077852. S2CID224314102.
Bartoli, F; Cioni, RM; Callovini, T; Cavaleri, D; Crocamo, C; Carrà, G (17 May 2021). "The kynurenine pathway in schizophrenia and other mental disorders: Insight from meta-analyses on the peripheral blood levels of tryptophan and related metabolites". Schizophrenia Research. 232: 61–62. doi:10.1016/j.schres.2021.04.008. PMID34015557. S2CID235074432.
Cheminal R, Echenne B, Bellet H, Duran M (1996). "Congenital non-progressive encephalopathy and deafness with intermittent episodes of coma and hyperkynureninuria". Journal of Inherited Metabolic Disease. 19 (1): 25–30. doi:10.1007/BF01799345. PMID8830173. S2CID810814.
Salih MA, Bender DA, McCreanor GM (November 1985). "Lethal familial pellagra-like skin lesion associated with neurologic and developmental impairment and the development of cataracts". Pediatrics. 76 (5): 787–793. doi:10.1542/peds.76.5.787. PMID4058988. S2CID11014655.