Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Shintaro Saito"'
Autor:
Kazuro Kaise, Kaoru Yoshinaga, Hiroshi Fukazawa, Makiko Yamamoto, Toshiro Sakurada, Katsumi Yoshida, Koki Mori, Shintaro Saito, Nobuko Kaise
Publikováno v:
Endocrinologia japonica. 38(4)
The outcome of 131I therapy for 109 patients with Gravest disease was analysed according to pretreatment laboratory data including thyrotropin receptor antibody (TRAb) activities. Forty-five percent of patients became euthyroid, and 13% of patients b
Autor:
Shintaro Saito, Hiroshi Fukazawa, Makiko Yamamoto, Kaoru Yoshinaga, Sadao Takase, Takashi Nomura, Nobuko Kaise, Kazuro Kaise, Katsumi Yoshida, Toshiro Sakurada
Publikováno v:
Clinical endocrinology. 32(4)
In order to investigate endocrine disturbances in patients with myotonic dystrophy (MD), 12 patients and 20 normal controls were studied. All patients were clinically euthyroid and there were no significant differences between circulating levels (mea
Autor:
SHINTARO SAITO, RIKIYA ABE, TOSHIRO SAKURADA, KATSUMI YOSHIDA, MICHIO KIMURA, MAKIKO YAMAMOTO, KAZUO KAISE, NOBUKO KAISE, KAORU YOSHINAGA
Publikováno v:
The Tohoku Journal of Experimental Medicine. 122:229-235
Patients with breast cancer were studied with regard to changes in the levels of serum thyroxine (T4) and serum triidothyronine (T3) after intramuscular administration of TSH for three days to investigate the thyroid reserve in these patients. The ch
Publikováno v:
Metabolism. 28:659-662
Thyroid peroxidase (TPO) activity was measured spectrophotometrically according to Hosoya's guaiacol method. The mean TPO activity in ten patients with Hashimoto's thyroiditis was 19.8 +/- 7.6 (mean +/- SE) in an arbitrary unit, which was not signifi
Autor:
Katsumi Yoshida, Tohru Yamaguchi, Kaoru Yoshinaga, Makiko Yamamoto, Shintaro Saito, Toshiro Sakurada, Yohichiro Sasai
Publikováno v:
The Tohoku Journal of Experimental Medicine. 115:155-165
Case 1 showed recurrence of hyperthyroidism accompanied by pretibial myxedema and digital clubbing 14 years after thyroidectomy for Graves' disease. Case 2 had had pretibial myxedema for the past 20 years and myxedema tuberosum at the right shoulder
Autor:
Katsumi Yoshida, Hiroshi Furazawa, Hirofumi Kitaora, Kazuro Kaise, Yamamoto M, Toshiro Sakurada, Nobuko Kaise, Shintaro Saito, Kaoru Yoshinaga
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 55:185-188
Serum absolute free T4 (AFT4) and T3 (AFT3) concentrations were studied in 10 patients with subacute thyroiditis whose total serum T4 levels were elevated, and values were compared with those obtained in 10 patients with untreated Graves' disease, wh
Publikováno v:
The Tohoku Journal of Experimental Medicine. 119:103-113
An 8-year-old boy with goiter and bilateral nerve deafness had a 46% discharge of radioiodine after thiocyanate administration. He was clinically euthyroid. Although the serum total T4 was low (2.4 mug/100 ml) and TSH was significantly high (181 muU/
Autor:
Yoshinori Kiso, Yoichi Itagaki, Tsunehiro Arai, Kunihiko Hanew, Shintaro Saito, Nobuko Kaise, Makiko Yamamoto, Kazuro Kaise, Katsumi Yoshida, Toshiro Sakurada, Kaoru Yoshinaga
Publikováno v:
The Tohoku Journal of Experimental Medicine. 157:69-78
A 22-year old man with a goiter and clinical manifestations of mild thyrotoxicosis (finger tremor, palpitation, tachycardia) was diagnosed as a syndrome of inappropriate secretion of TSH. Serum concentrations of T4, free T4, T3 and TSH were 24.1 micr
Autor:
Hiroshi Fukazawa, Makiko Yamamoto, Shintaro Saito, Katsumi Yoshida, Kaoru Yoshinaga, Toshiro Sakurada, Kazuro Kaise, Nobuko Kaise, Kitaoka H
Publikováno v:
Acta Endocrinologica. 102:531-534
A 36 year old man with a diffuse goitre, signs of mild hypothyroidism, strikingly low levels of T4 (0.9 μg/dl) and T3 (24 ng/dl), elevated TSH (140 μU/ml) and elevated microsomal haemagglutination antibody (MCHA, 1:409 600), subsequently became non
Autor:
Keigo Yasuda, Toru Yamaguchi, Makiko Yamamoto, Seiju Onodera, Makio Okuyama, Kaoru Yoshinaga, Katsuhiko Kato, Kosuke Oikawa, Toshiro Sakurada, Shintaro Saito, Tokutaro Sato, Hiroshi Ito, Takahiko Takenouchi
Publikováno v:
The Tohoku Journal of Experimental Medicine. 114:287-294
Dyschondrosteosis, also known as Leri-Weill syndrome, is characterized by mesomelic dwarfism and Madelung's deformity. The association of this disorder with various endocrine, metabolic or intelligence abnormalities has not been described. We have, h