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The Journal of Clinical Endocrinology and Metabolism|May 28, 2020
Targeted Next-Generation Sequencing for Congenital Hypothyroidism With Positive Neonatal TSH ScreeningTakeshi Yamaguchi, Akie Nakamura, Kanako Nakayama, et al.
Endocrine Journal|March 5, 2015
Clinical, biochemical, and genetic features of non-classical 21-hydroxylase deficiency in Japanese childrenKenichi Kashimada, Tomohiro Ishii, Keisuke Nagasaki, et al.
Neuro-Oncology|July 10, 2008
Role of surgery for optic pathway/hypothalamic astrocytomas in childrenYutaka Sawamura, Kyousuke Kamada, Yuuta Kamoshima, et al.
Endocrine Journal|November 14, 2007
Novel SLC12A1 (NKCC2) mutations in two families with Bartter syndrome type 1Masanori Adachi, Yumi Asakura, Yoshiaki Sato, et al.
AJP Reports|August 15, 2013
Nephrocalcinosis and placental findings in neonatal bartter syndromeHidehiko Maruyama, Yoko Shinno, Kaori Fujiwara, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 12, 2016
High prevalence of DUOX2 mutations in Japanese patients with permanent congenital hypothyroidism or transient hypothyroidismKumihiro Matsuo, Yusuke Tanahashi, Tokuo Mukai, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|April 1, 2014
Identification of IgG-κ type macroprolactin found in the serum of an 8-year-old girlKeiichi Nakano, Takanori Moriyama, Keiko Yasuda, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|August 31, 2013
Development of endometrial carcinoma in a patient with leprechaunism (donohue syndrome)Wakako Jo, Satoko Sudo, Akie Nakamura, et al.
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