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Juvenile-onset hereditary pheochromocytoma-paraganglioma syndrome.
Sugisawa C, Okada Y, Arao T, Mori H, Nishida K, Isobe K, Takekoshi K, Tanaka Y. Sugisawa C, et al. Intern Med. 2013;52(2):281-4. doi: 10.2169/internalmedicine.52.8223. Epub 2013 Jan 15. Intern Med. 2013. PMID: 23318864 Free article.
Clinicopathological study of SDHB mutation-related pheochromocytoma and sympathetic paraganglioma.
Kimura N, Takekoshi K, Horii A, Morimoto R, Imai T, Oki Y, Saito T, Midorikawa S, Arao T, Sugisawa C, Yamada M, Otuka Y, Kurihara I, Sugano K, Nakane M, Fukuuchi A, Kitamoto T, Saito J, Nishikawa T, Naruse M. Kimura N, et al. Among authors: sugisawa c. Endocr Relat Cancer. 2014 May 6;21(3):L13-6. doi: 10.1530/ERC-13-0530. Print 2014 Jun. Endocr Relat Cancer. 2014. PMID: 24659481 No abstract available.
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: sugisawa c. 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.
Immunohistochemical Expression of Choline Acetyltransferase and Catecholamine-Synthesizing Enzymes in Head-and-Neck and Thoracoabdominal Paragangliomas and Pheochromocytomas.
Kimura N, Shiga K, Kaneko KI, Oki Y, Sugisawa C, Saito J, Tawara S, Akahori H, Sogabe S, Yamashita T, Takekoshi K, Naruse M, Katabami T. Kimura N, et al. Among authors: sugisawa c. Endocr Pathol. 2021 Dec;32(4):442-451. doi: 10.1007/s12022-021-09694-x. Epub 2021 Nov 6. Endocr Pathol. 2021. PMID: 34743284
Therapeutic efficacy and limitations of potassium iodide for patients newly diagnosed with Graves' disease.
Suzuki N, Yoshimura Noh J, Sugisawa C, Hoshiyama A, Hiruma M, Kawaguchi A, Morisaki M, Ohye H, Suzuki M, Matsumoto M, Kunii Y, Yoshihara A, Watanabe N, Sugino K, Ito K. Suzuki N, et al. Among authors: sugisawa c. Endocr J. 2020 Jun 29;67(6):631-638. doi: 10.1507/endocrj.EJ19-0379. Epub 2020 Mar 18. Endocr J. 2020. PMID: 32188795 Free article. Clinical Trial.
Clinical characteristics and efficacy of pioglitazone in a Japanese patient with familial partial lipodystrophy due to peroxisome proliferator-activated receptor γ gene mutation.
Iizaka T, Kodama E, Mikura K, Iida T, Imai H, Hashizume M, Kigawa Y, Sugisawa C, Tadokoro R, Endo K, Otsuka F, Isoda M, Ebihara K, Ishibashi S, Nagasaka S. Iizaka T, et al. Among authors: sugisawa c. Endocr J. 2023 Jan 30;70(1):69-76. doi: 10.1507/endocrj.EJ22-0140. Epub 2022 Sep 29. Endocr J. 2023. PMID: 36171144 Free article.
33 results