Zobrazeno 1 - 10
of 66
pro vyhledávání: '"Kanji Nagashima"'
Autor:
Kazumichi Onigata, Tomohisa Nagashima, Masatomo Mori, Tadashi Morimura, Kanji Nagashima, Akihiro Morikawa, Masami Murakami
Publikováno v:
Thyroid. 11:551-559
We describe Japanese siblings with resistance to thyrotropin (TSH) who are compound heterozygotes for two novel mutations in the TSH receptor gene. The affected siblings had increased serum TSH, normal serum thyroid hormones, and normal positioned bu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff79faf35cd1beba00c79aff353b1e49
https://doi.org/10.1089/105072501750302859
https://doi.org/10.1089/105072501750302859
Autor:
Kazumichi Onigata, Yoko Takano, Reiko Saga, Kazushi Tamura, Akihiro Morikawa, Kanji Nagashima
Publikováno v:
The KITAKANTO Medical Journal. 49:361-364
発熱, 体重増加不良, 頻尿などの症状にて発症した生後3カ月の乳児糖尿病児に対し, インスリン持続静注療法にて初期治療を行い, その後皮下注射法に移行した.哺乳量や哺乳時間が一定で
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6586eea22584af1120d5c2fde2e0bd9
https://doi.org/10.2974/kmj.49.361
https://doi.org/10.2974/kmj.49.361
Autor:
Kanji Nagashima, Yoko Nomura, Akihiro Morikawa, Tomohisa Nagashima, Yukie Suzuki, Kazumichi Onigata
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 83:199-202
A genetic disorder in cytochrome P450c17 results in 17 alpha-hydroxylase/17,20-lyase deficiency. In the present study, a Japanese patient with 17 alpha-hydroxylase/17,20-lyase deficiency underwent molecular analysis. The patient presented with comple
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d75e71eb405d10dc466484057556f176
https://doi.org/10.1210/jcem.83.1.4516
https://doi.org/10.1210/jcem.83.1.4516
Publikováno v:
The KITAKANTO Medical Journal. 48:163-166
20代および30代前半の若年女性糖尿病患者における骨密度を測定し, その異常の有無を調べた.また, 同患者における血清および尿中骨代謝マーカーを測定し, 骨病変ならびに骨形成, 吸収マ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1fad8c8df591ab27c4f25f1cf6187759
https://doi.org/10.2974/kmj.48.163
https://doi.org/10.2974/kmj.48.163
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 82:3281-3284
The serum leptin concentration reflects the amount of adipose tissue in the body. Although fat deposition in the fetus in the third trimester markedly increases, the role of leptin during pregnancy has not been clarified. In the present study, whethe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eccb450334853485bf824b4f06383a01
https://doi.org/10.1210/jcem.82.10.4321
https://doi.org/10.1210/jcem.82.10.4321
Publikováno v:
The KITAKANTO Medical Journal. 46:239-247
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8f09cdb7dc9761ed4e0a47a286322c3
https://doi.org/10.2974/kmj1951.46.239
https://doi.org/10.2974/kmj1951.46.239
Autor:
Hiroshi Miyake, Hideki Yagi, Kazumichi Onigata, Akihiro Morikawa, Kanji Nagashima, Shigenori Yutani
Publikováno v:
Clinical Pediatric Endocrinology. 5:73-78
We developed a mass screening system for short stature in elementary school children. The subjects of this mass screening were 153, 679 pupils. This screening was done in two steps. In the primary screening, children with possible short stature were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::42dc8740084a67f290bab16ccffa2b0d
https://doi.org/10.1297/cpe.5.73
https://doi.org/10.1297/cpe.5.73
Autor:
Yoko Nomura, Kanji Nagashima, Shigenori Yutani, Akihiro Morikawa, Kazumichi Onigata, Ryo Ogawa, Hideki Yagi, Tomohisa Nagashima
Publikováno v:
Pediatrics International. 37:706-709
The unusual case of a Japanese newborn XX male is presented. Examination of chromosomes in amniotic fluid cells had shown a normal female karyotype (46,XX), but ultrasonography revealed a penis and a scrotum. The neonate had normal male external geni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b32a8c66f1eb16cfae50500396f50ec5
https://doi.org/10.1111/j.1442-200x.1995.tb03410.x
https://doi.org/10.1111/j.1442-200x.1995.tb03410.x
Autor:
Hideki Yagi, Akihiro Sakurai, Kanji Nagashima, Kiyoshi Hashizume, Akihiro Morikawa, Tomohisa Nagashima, Kazumichi Onigata, Yoko Nomura
Publikováno v:
Thyroid. 5:355-358
Resistance to thyroid hormone (RTH) is characterized by variable tissue hyporesponsiveness to thyroid hormones. Recently, a large number of different point mutations have been identified in the c-erbA beta thyroid hormone receptor (TR beta) in subjec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4fd00d4625b0a56e7261d3ad4863f60
https://doi.org/10.1089/thy.1995.5.355
https://doi.org/10.1089/thy.1995.5.355
Autor:
Kanji Nagashima, Ryo Ogawa, Yoko Nomura, Hideki Yagi, Tomohisa Nagashima, Akihiro Morikawa, Kazumichi Onigata
Publikováno v:
Clinical Pediatric Endocrinology. 4:149-154
We report a patient who had the complete androgen insensitivity syndrome (CAIS) associated with a novel point mutation in the ligand-binding domain of the androgen receptor (AR) gene.The patient was 12 years old with complete female external genitali
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d6bd0f202ac139e875dd6e8f09f2329
https://doi.org/10.1297/cpe.4.149
https://doi.org/10.1297/cpe.4.149