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Genetic basis of fasting hyperbilirubinemia.
Ishihara T, Gabazza EC, Adachi Y, Sato H, Maruo Y. Ishihara T, et al. Among authors: adachi y. Gastroenterology. 1999 May;116(5):1272. doi: 10.1016/s0016-5085(99)70038-7. Gastroenterology. 1999. PMID: 10220526 No abstract available.
Role of UGT1A1 mutation in fasting hyperbilirubinemia.
Ishihara T, Kaito M, Takeuchi K, Gabazza EC, Tanaka Y, Higuchi K, Ikoma J, Watanabe S, Sato H, Adachi Y. Ishihara T, et al. Among authors: adachi y. J Gastroenterol Hepatol. 2001 Jun;16(6):678-82. doi: 10.1046/j.1440-1746.2001.02495.x. J Gastroenterol Hepatol. 2001. PMID: 11422622
Mutation of UGT1A1 gene in a case of Crigler-Najjar syndrome type II.
Ishihara T, Sato H, Fukui S, Kagawa K, Kaito M, Gabazza EC, Adachi Y. Ishihara T, et al. Among authors: adachi y. Am J Gastroenterol. 1999 Jun;94(6):1711-2. doi: 10.1111/j.1572-0241.1999.1711a.x. Am J Gastroenterol. 1999. PMID: 10364060 No abstract available.
The genetic basis of Gilbert's syndrome.
Sato H, Adachi Y, Koiwai O. Sato H, et al. Among authors: adachi y. Lancet. 1996 Mar 2;347(9001):557-8. doi: 10.1016/s0140-6736(96)91266-0. Lancet. 1996. PMID: 8596313 No abstract available.
2,708 results