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Type 4B hereditary hemochromatosis due to heterozygous p.D157A mutation in SLC40A1 complicated with hypopituitarism.
Honma Y, Karasuyama T, Kumamoto K, Shimajiri S, Toki Y, Tatsumi Y, Sumida K, Koikawa K, Morino K, Oe S, Miyagawa K, Yamasaki M, Shibata M, Abe S, Ikuta K, Hayashi H, Harada M. Honma Y, et al. Among authors: hayashi h. Med Mol Morphol. 2021 Mar;54(1):60-67. doi: 10.1007/s00795-020-00259-1. Epub 2020 Jun 30. Med Mol Morphol. 2021. PMID: 32607777
Increase in P-glycoprotein accompanied by activation of protein kinase Calpha and NF-kappaB p65 in the livers of rats with streptozotocin-induced diabetes.
Kameyama N, Arisawa S, Ueyama J, Kagota S, Shinozuka K, Hattori A, Tatsumi Y, Hayashi H, Takagi K, Wakusawa S. Kameyama N, et al. Among authors: hayashi h. Biochim Biophys Acta. 2008 May;1782(5):355-60. doi: 10.1016/j.bbadis.2008.02.005. Epub 2008 Mar 4. Biochim Biophys Acta. 2008. PMID: 18346469 Free article.
Special stain and X-ray probe microanalysis of livers with Wilson disease.
Hayashi H, Fujita Y, Tatsumi Y, Hattori A, Hayashi K, Katano Y, Wakusawa S, Yano M, Itoh M, Mizutani N, Goto H. Hayashi H, et al. Among authors: hayashi k. Hepatol Res. 2009 Jun;39(6):563-8. doi: 10.1111/j.1872-034X.2009.00491.x. Epub 2009 Feb 25. Hepatol Res. 2009. PMID: 19254344
Current state of Wilson disease patients in central Japan.
Tatsumi Y, Hattori A, Hayashi H, Ikoma J, Kaito M, Imoto M, Wakusawa S, Yano M, Hayashi K, Katano Y, Goto H, Okada T, Kaneko S. Tatsumi Y, et al. Among authors: hayashi k, hayashi h. Intern Med. 2010;49(9):809-15. doi: 10.2169/internalmedicine.49.2931. Epub 2010 Apr 30. Intern Med. 2010. PMID: 20453399 Free article.
Measurement of serum hepcidin-25 levels as a potential test for diagnosing hemochromatosis and related disorders.
Kaneko Y, Miyajima H, Piperno A, Tomosugi N, Hayashi H, Morotomi N, Tsuchida K, Ikeda T, Ishikawa A, Ota Y, Wakusawa S, Yoshioka K, Kono S, Pelucchi S, Hattori A, Tatsumi Y, Okada T, Yamagishi M. Kaneko Y, et al. Among authors: hayashi h. J Gastroenterol. 2010 Nov;45(11):1163-71. doi: 10.1007/s00535-010-0259-8. Epub 2010 Jun 9. J Gastroenterol. 2010. PMID: 20533066
Potential of the international scoring system for the diagnosis of Wilson disease to differentiate Japanese patients who need anti-copper treatment.
Tatsumi Y, Shinohara T, Imoto M, Wakusawa S, Yano M, Hayashi K, Hattori A, Hayashi H, Shimizu A, Ichiki T, Nakashima S, Katano Y, Goto H. Tatsumi Y, et al. Among authors: hayashi k, hayashi h. Hepatol Res. 2011 Sep;41(9):887-96. doi: 10.1111/j.1872-034X.2011.00835.x. Epub 2011 Jun 28. Hepatol Res. 2011. PMID: 21707886
Identification of a novel mutation in the HAMP gene that causes non-detectable hepcidin molecules in a Japanese male patient with juvenile hemochromatosis.
Hattori A, Tomosugi N, Tatsumi Y, Suzuki A, Hayashi K, Katano Y, Inagaki Y, Ishikawa T, Hayashi H, Goto H, Wakusawa S. Hattori A, et al. Among authors: hayashi k, hayashi h. Blood Cells Mol Dis. 2012 Mar 15;48(3):179-82. doi: 10.1016/j.bcmd.2012.01.002. Epub 2012 Jan 30. Blood Cells Mol Dis. 2012. PMID: 22297252
6,597 results