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Hereditary pheochromocytoma/paraganglioma syndrome with a novel mutation in the succinate dehydrogenase subunit B gene in a Japanese family: two case reports.
Hirose R, Tsurutani Y, Sugisawa C, Inoue K, Suematsu S, Nagata M, Hasegawa N, Kakuta Y, Yonamine M, Takekoshi K, Kimura N, Saito J, Nishikawa T. Hirose R, et al. Among authors: takekoshi k. J Med Case Rep. 2021 May 22;15(1):282. doi: 10.1186/s13256-021-02852-z. J Med Case Rep. 2021. PMID: 34020699 Free PMC article.
Prevalence of Germline Variants in a Large Cohort of Japanese Patients with Pheochromocytoma and/or Paraganglioma.
Yonamine M, Wasano K, Aita Y, Sugasawa T, Takahashi K, Kawakami Y, Shimano H, Nishiyama H, Hara H, Naruse M, Okamoto T, Matsuda T, Kosugi S, Horiguchi K, Tanabe A, Watanabe A, Kimura N, Nakamura E, Sakurai A, Shiga K, Takekoshi K. Yonamine M, et al. Among authors: takekoshi k. Cancers (Basel). 2021 Aug 9;13(16):4014. doi: 10.3390/cancers13164014. Cancers (Basel). 2021. PMID: 34439168 Free PMC article.
Synonymous but Not Silent: A Synonymous VHL Variant in Exon 2 Confers Susceptibility to Familial Pheochromocytoma and von Hippel-Lindau Disease.
Flores SK, Cheng Z, Jasper AM, Natori K, Okamoto T, Tanabe A, Gotoh K, Shibata H, Sakurai A, Nakai T, Wang X, Zethoven M, Balachander S, Aita Y, Young W, Zheng S, Takekoshi K, Nakamura E, Tothill RW, Aguiar RCT, Dahia PLM. Flores SK, et al. Among authors: takekoshi k. J Clin Endocrinol Metab. 2019 Sep 1;104(9):3826-3834. doi: 10.1210/jc.2019-00235. J Clin Endocrinol Metab. 2019. PMID: 30946460 Free PMC article.
Plasma free metanephrines in the diagnosis of pheochromocytoma: diagnostic accuracy and strategies for Japanese patients.
Tanaka Y, Isobe K, Ma E, Imai T, Kikumori T, Matsuda T, Maeda Y, Sakurai A, Midorikawa S, Hataya Y, Kato T, Kamide K, Ikeda Y, Okada Y, Adachi M, Yanase T, Takahashi H, Yokoyama C, Arai Y, Hashimoto K, Shimano H, Hara H, Kawakami Y, Takekoshi K. Tanaka Y, et al. Among authors: takekoshi k. Endocr J. 2014;61(7):667-73. doi: 10.1507/endocrj.ej13-0277. Epub 2014 May 28. Endocr J. 2014. PMID: 24871964 Free article.
Novel germline variant of TMEM127 gene in a patient with familial pheochromocytoma.
Saitoh K, Yonemoto T, Usui T, Takekoshi K, Suzuki M, Nakashima Y, Yoshimura K, Kosugi R, Ogawa T, Inoue T. Saitoh K, et al. Among authors: takekoshi k. Endocrinol Diabetes Metab Case Rep. 2017 Apr 6;2017:17-0014. doi: 10.1530/EDM-17-0014. eCollection 2017. Endocrinol Diabetes Metab Case Rep. 2017. PMID: 28458909 Free PMC article.
150 results