Zobrazeno 1 - 10
of 176
pro vyhledávání: '"Takao, Obara"'
Publikováno v:
SAGE Open Medical Case Reports, Vol 9 (2021)
We report a 21-year-old woman with Turner’s syndrome, Graves’ disease and primary hyperparathyroidism. At 12 years of age, she was of short stature, and was diagnosed with Turner’s syndrome and treated with growth hormone. At the age of 17 year
Externí odkaz:
https://doaj.org/article/e6c7b518d44e4eb2a58daa943622d003
Publikováno v:
SAGE Open Medical Case Reports, Vol 9 (2021)
SAGE Open Medical Case Reports
SAGE Open Medical Case Reports
We report a 21-year-old woman with Turner’s syndrome, Graves’ disease and primary hyperparathyroidism. At 12 years of age, she was of short stature, and was diagnosed with Turner’s syndrome and treated with growth hormone. At the age of 17 year
Autor:
Luqman Sulaiman, Felix Haglund, Jamileh Hashemi, Takao Obara, Jörgen Nordenström, Catharina Larsson, C Christofer Juhlin
Publikováno v:
PLoS ONE, Vol 7, Iss 9, p e46325 (2012)
Mutations in the hyperparathyroidism type 2 (HRPT2/CDC73) gene and alterations in the parafibromin protein have been established in the majority of parathyroid carcinomas and in subsets of parathyroid adenomas. While it is known that CDC73-mutated pa
Externí odkaz:
https://doaj.org/article/506d7ad0a0ef4f85861e4be472e3ad0c
Autor:
Yoshiaki Azuma, Takao Obara, Kishiko Nakajima, Seiichi Kosaka, Kazue Takano, Ken-ichi Umino, Kanji Sato
Publikováno v:
Journal of Bone and Mineral Metabolism. 27:224-233
The pathogenesis of primary hyperparathyroidism (I degrees -HPT) and secondary hyperparathyroidism (II degrees -HPT) remains to be elucidated. To characterize their pathophysiology, we investigated the effects of calcium and phosphate on cell prolife
Publikováno v:
Acta Histochemica et Cytochemica
Microsomal prostaglandin E(2) synthase-1 (mPGES-1) is an inducible enzyme that catalyzes the conversion of prostaglandin (PG) H(2) to PGE(2) in downstream of cyclooxygenase-2 (COX-2). Recent studies have obtained in vitro evidence that PGE(2) partici
Autor:
Takao Obara, Toshiro Seki, Tsuyoshi Shiga, Kazue Takano, Hitomi Kodama, Kazuko Yamazaki, Kanji Sato, Yoko Omi, Hiroshi Kasanuki, Emiko Yamada
Publikováno v:
Internal Medicine. 47:757-762
We report the treatment of four thyrotoxic patients. Two were cases of type I amiodarone-induced thyrotoxicosis (AIT) treated with methimazole. The third Graves' disease patient, who became hypothyroid 25 years after subtotal thyroidectomy, developed
Publikováno v:
Surgery Today. 37:884-887
Water-clear cell parathyroid adenoma is an exceedingly rare tumor, composed exclusively of tumor cells with abundant foamy cytoplasm. A combination of hyperparathyroidism and neurofibromatosis type 1 (NF1) is also a rare phenomenon. We report an 18-y
Autor:
Kazue Takano, Takao Obara, Emiko Yamada, Tomoaki Mitsuhashi, Misako Matsumoto, Kanji Sato, Koichi Suzuki, Fumihiko Takeshita, Tetsu Yamada, Kazuko Yamazaki
Publikováno v:
Endocrinology. 148:3226-3235
Although viral infection is thought to be associated with subacute thyroiditis and probably with autoimmune thyroid disease, possible changes in thyroid function during the prodromal period of infection or subclinical infection remain largely unknown
Autor:
Yoko Omi, Masatoshi Iihara, Rumi Suzuki, Takahiro Okamoto, Hitomi Kodama, Akiko Kawamata, Yukio Ito, Takao Obara
Publikováno v:
Nihon Rinsho Geka Gakkai Zasshi (Journal of Japan Surgical Association). 68:2697-2706
副腎癌の臨床的特徴と治療成績について報告する. 対象は当科にて初回治療した副腎癌9例で, 内訳は原発性アルドステロン症3例, 男性化腫瘍2例, クッシング症候群4例である. そのうちア
Autor:
Naganari Ohkura, Takao Obara, Toshihiko Tsukada, Yuko Nagamura, Hiroko Yaguchi, Atsushi Fukuuchi
Publikováno v:
Japanese Journal of Clinical Oncology. 36:739-744
Multiple endocrine neoplasia type 1 is an autosomal dominant cancer syndrome characterized by pituitary, parathyroid and enteropancreatic endocrine tumors, which is caused by germline mutations of the tumor suppressor gene MEN1. In the case reported