Published papers
Hasegawa, Tomonobu
261-280 items (total 510)
グルココルチコイド反応性アルドステロン症(GRA)
- Author
- 林美恵、長谷川奉延
- Publication Title
- Start Page 189 - End Page 192 (Publication Date）2012）
小児科領域から見た小児の成長障害
- Author
- 有安大典、長谷川奉延
- Publication Title
- Start Page 1202 - End Page 1206 (Publication Date）2012）
先天性副腎ステロイド産生異常症の最近の話題
- Author
- HASEGAWA TOMONOBU
- Publication Title
- Start Page 1989 - End Page 1995 (Publication Date）2012）
マッキュン・オルブライト症候群
- Author
- HASEGAWA TOMONOBU
- Publication Title
- Start Page 1312 - End Page 1313 (Publication Date）2012）
副腎皮質機能低下症のアルゴリズム
- Author
- HASEGAWA TOMONOBU
- Publication Title
- Start Page 588 - End Page 592 (Publication Date）2012）
なぜ今、日常診療に小児内分泌学か？
- Author
- HASEGAWA TOMONOBU
- Publication Title
- Start Page 9 (Publication Date）2012）
子どものホルモンの病気をご存じですか？
- Author
- HASEGAWA TOMONOBU
- Publication Title
- Start Page 25 (Publication Date）2012）
ホルモンが関係する病気
- Author
- HASEGAWA TOMONOBU
- Publication Title
- Start Page 98 - End Page 101 (Publication Date）2012）
内分泌器官の器官形成とその異常
- Author
- 鳴海覚志、長谷川奉延
- Publication Title
- Start Page 483 - End Page 489 (Publication Date）2012）
成長曲線を正しく使おう―身長・体重・頭囲・座高・腹囲・伸展陰茎長・精巣容積・BMI―
- Author
- 井ノ口美香子、長谷川奉延
- Publication Title
- Start Page 353 - End Page 361 (Publication Date）2012）
Gradual loss of ACTH due to a novel mutation in LHX4: Comprehensive mutation screening in Japanese patients with congenital hypopituitarism.
- Author
- Takagi M, Ishii T, Inokuchi M, Amano N, Asakura Y, Muroya K, Hasegawa Y, Adachi M, Hasegawa T
- Publication Title
- Magazine name PLos One Start Page e46008 (Publication Date）2012）
- Authorship Category
- Joint Work
Functional characterization of four novel PAX 8 mutations causing congenital hypothyroidism: New evidence for haploinsufficiency as a a disease mechanism.
- Author
- Narumi S, Araki S, Hori N, Muroya K, Yamamoto Y, Asakura Y, Adachi M, Hasegawa T
- Publication Title
- Magazine name Eur J Endocrinol Start Page 625 - End Page 632 (Publication Date）2012）
- Authorship Category
- Joint Work
Recurrence of osteogenesis imperfect due to maternal mosaicism of a novel COL1A1 mutation.
- Author
- Yamada T, Takagi M, Nishimura G, Akaishi R, Furuta I, Morikawa M, Yamada T, Cho K, Sawai H, Ikegawa S, Hasegawa T, Minakami H
- Publication Title
- Magazine name Am J Med Genet A Start Page 2969 - End Page 2971 (Publication Date）2012）
- Authorship Category
- Joint Work
PAPSS2 mutations cause autosomal recessive brachyolmia.
- Author
- Miyake N, Elcioglu NH, Iida A, Isguven P, Dai J, Murakami N, Takamura K, Cho T-J, Kim O-H, Hasegawa T, Nagai T, Ohashi H, Nishimura G, Matsumoto N, Ikegawa S
- Publication Title
- Magazine name J Med Genet Start Page 533 - End Page 538 (Publication Date）2012）
- Authorship Category
- Joint Work
Hypoglycemia associated with L-asparaginase in acute lymphoblastic leukemia treatment: a case report.
- Author
- Tanaka R, Osumi T, MiharuM, Ishii T, Hasegawa T, Takahashi T, Shimada H
- Publication Title
- Magazine name Exp Hematol Oncol Start Page 8 (Publication Date）2012）
- Authorship Category
- Joint Work
Prenatal diagnosis of osteogenesis imperfecta type II by three-dimensional computed tomography (CT): the current state of fetal CT.
- Author
- Akizawa Y, Nishimura G, Hasegawa T, Takagi M, Kawamichi Y, Matsuda Y, Matsui H, Saito K
- Publication Title
- Magazine name Cong Anomalies(Kyoto) Start Page 203 - End Page 206 (Publication Date）2012）
- Authorship Category
- Joint Work
A novel mutation in LEPRE1 that eliminates only the KDEL ER- retrieval sequence causes non-lethal osteogenesis imperfect.
- Author
- Takagi M, Ishii T, Barnes AM, Weis MA, Amano N, Tanaka M, Fukuzawa R, Nishimura G, Eyre DR, Marini JC, Hasegawa T
- Publication Title
- Magazine name PLos One Start Page e36809 (Publication Date）2012）
- Authorship Category
- Joint Work
A genome-wide expression profile of adrenocortical cells in knockout mice lacking steroidogenic acute regulatory protein.
- Author
- Ishii T, Mitsui T, Suzuki S, Matsuzaki Y, Hasegawa T
- Publication Title
- Magazine name Endocrinol Start Page 2714 - End Page 2723 (Publication Date）2012）
- Authorship Category
- Joint Work
Favorable impact on growth hormone treatment on cholesterol levels in Turner syndrome.
- Author
- Kohno H, Igarashi Y, Ozono K, Ohyama K, Ogawa M, Osada H, Onigata K, Kanzaki S, Seino Y, Takahashi H, Tajima T, Tachibana K, Tanaka H, Nishi Y, Hasegawa T, Fujieda K, Fujita K, Horikawa R, Yokoya S, Yorifuji T, Tanaka T
- Publication Title
- Magazine name Clin Pediatr Endocrinol Start Page 29 - End Page 34 (Publication Date）2012）
- Authorship Category
- Joint Work
A case of Rabson-Mendenhall syndrome with a novel mutation in the tyrosine kinase domain of the insulin receptor gene complicated by medullary sponge kidney.
- Author
- Abe Y, Sato T, Takagi M, Watanabe T, Nagayama Y, Hasegawa T, Abe T
- Publication Title
- Magazine name J Pediatr Endocr Met Start Page 587 - End Page 590 (Publication Date）2012）
- Authorship Category
- Joint Work