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Endocrine Journal|February 16, 2018
A case report of thyroid metastasis from p16-positive oropharyngeal squamous cell carcinomaMasao Takenobu, Sueyoshi Moritani, Kana Yoshioka, et al.Endocrine Journal|February 14, 2018
Validation of simple indexes for nonalcoholic fatty liver disease in western China: a retrospective cross-sectional studyJinzhou Zhu, Mingqing He, Yong Zhang, et al.Endocrine Journal|December 5, 2017
Re-evaluation of MIB-1 immunostaining for diagnosing hyalinizing trabecular tumour of the thyroid: semi-automated techniques with manual antigen retrieval are more accurate than fully automated techniquesNami Takada, Mitsuyoshi Hirokawa, Chiho Ohbayashi, et al.Endocrine Journal|November 10, 2017
Mismatch between fetal sexing and birth phenotype: a case of complete androgen insensitivity syndromeKeisuke Yoshii, Yasuhiro Naiki, Yumiko Terada, et al.Endocrine Journal|November 23, 2017
Impact of macroprolactin on galactorrhea and the rate of patients possibly affected by macroprolactinKohzo Aisaka, Fujiko Tsuchiya, Masami Sueta, et al.Endocrine Journal|July 14, 2017
Efficacy and safety of octreotide for the treatment of congenital hyperinsulinism: a prospective, open-label clinical trial and an observational study in Japan using a nationwide registryYuki Hosokawa, Rie Kawakita, Susumu Yokoya, et al.Endocrine Journal|July 14, 2017
Expression of aldo-keto reductase family 1, member C14 during ovulation in the ratPhuong T M Dam, You-Jee Jang, Ja-Yeon Kim, et al.Endocrine Journal|December 21, 2018
Change of surgical strategy for Graves' disease from subtotal thyroidectomy to total thyroidectomy: a single institutional experienceKiminori Sugino, Mitsuji Nagahama, Wataru Kitagawa, et al.Endocrine Journal|December 21, 2018
Implications of thyroid autoimmunity in infertile women with subclinical hypothyroidism in the absence of both goiter and anti-thyroid antibodies: lessons from three casesAko Oiwa, Kesami Minemura, Shin-Ichi Nishio, et al.Endocrine Journal|September 9, 2006
Sporadic congenital hyperthyroidism due to a germline mutation in the thyrotropin receptor gene (Leu 512 Gln) in a Japanese patientEijun Nishihara, Shuji Fukata, Akira Hishinuma, et al.Pageof 407