Search

Your search keyword '"Hatabu, Naomi"' showing total 6 results
Start Over Author "Hatabu, Naomi"
6 results on '"Hatabu, Naomi"'

2. Metacarpophalangeal pattern profile analysis for a 3‐month‐old infant with Feingold syndrome 2

Author

Isobe, Aiko, primary, Maeda, Naonori, additional, Fujita, Hisayo, additional, Banno, Sari, additional, Kageyama, Tomoka, additional, Hatabu, Naomi, additional, Sato, Rieko, additional, Suzuki, Eri, additional, Miharu, Masashi, additional, Komiyama, Osamu, additional, Nakashima, Moeko, additional, Matsunaga, Tatsuo, additional, Nishimura, Gen, additional, and Yamazawa, Kazuki, additional

Published
2020
Full Text
View/download PDF

3. A Familial Case of a Whole Germline CDC73 Deletion Discordant for Primary Hyperparathyroidism

Author

Hatabu, Naomi, primary, Katori, Naho, additional, Sato, Takeshi, additional, Maeda, Naonori, additional, Suzuki, Eri, additional, Komiyama, Osamu, additional, Tsutsui, Hidemitsu, additional, Nagao, Toshitaka, additional, Nakauchi-Takahashi, Hana, additional, Matsunaga, Tatsuo, additional, Ishii, Tomohiro, additional, Hasegawa, Tomonobu, additional, and Yamazawa, Kazuki, additional

Published
2019
Full Text
View/download PDF

4. Pubertal Development and Pregnancy Outcomes in 46,XX Patients With Nonclassic Lipoid Congenital Adrenal Hyperplasia

Author

Hatabu, Naomi, primary, Amano, Naoko, additional, Mori, Jun, additional, Hasegawa, Yukihiro, additional, Matsuura, Hiroki, additional, Sumitomo, Naofumi, additional, Nishizawa, Kazumichi, additional, Suzuki, Mariko, additional, Katakura, Satomi, additional, Kanamoto, Naokazu, additional, Kamimaki, Tsutomu, additional, Ishii, Tomohiro, additional, and Hasegawa, Tomonobu, additional

Published
2018
Full Text
View/download PDF

6. Pubertal Development and Pregnancy Outcomes in 46,XX Patients With Nonclassic Lipoid Congenital Adrenal Hyperplasia.

Author

Hatabu, Naomi, Amano, Naoko, Mori, Jun, Hasegawa, Yukihiro, Matsuura, Hiroki, Sumitomo, Naofumi, Nishizawa, Kazumichi, Suzuki, Mariko, Katakura, Satomi, Kanamoto, Naokazu, Kamimaki, Tsutomu, Ishii, Tomohiro, and Hasegawa, Tomonobu

Abstract

Lipoid congenital adrenal hyperplasia (LCAH) is characterized by a disorder of steroidogenesis in both adrenal glands and gonads. 46,XX patients with classic LCAH usually have thelarche and menarche but show anovulatory menstruations and subsequent premature menopause. Only three patients with classic LCAH have been reported to successfully achieve delivery with the aid of assisted reproductive therapies for conception and progesterone replacement therapy during early pregnancy. In contrast, pubertal development and pregnancy outcomes in patients with nonclassic LCAH have not been fully elucidated.

Published
2019
Full Text
View/download PDF

Catalog

Books, media, physical & digital resources
See catalog results