Published papers
Hasegawa, Tomonobu
441-460 items (total 510)
GATA3ハプロ不全の多彩な臨床像 11家系20症例の検討
- Author
- 室谷浩二、長谷川奉延、長谷川行洋、坪内肯二、中込美子、菊池信行、伊藤善也、藤田敬之助、深見真紀、緒方勤
- Publication Title
- Start Page 965 - End Page 970 (Publication Date）2004）
- Authorship Category
- Single Work
Testicular dysgenesis without adrenal insufficiency in a 46,XY patient with a heterozygous inactive mutation of steroidogenic factor-1.
- Author
- Hasegawa T, Fukami M, Sato N, Katsumata N, Sasaki G, Fukutani K, Morohashi K-i, Ogata T
- Publication Title
- Magazine name J Clin Endocrinol Metab Start Page 5930 - End Page 1935 (Publication Date）2004）
- Authorship Category
- Joint Work
Transient hyper17-OHPnemia unremated to cross-reactions with residual fetal adrenal cortex products.
- Author
- Mizuno H, Ohro Y, Sugiyama Y, Ito T, Hasegawa T, Homma K, Ueshiba H, Togari H.
- Publication Title
- Magazine name Hor Res Volume 61(Issue 5) Start Page 242-245 (Publication Date）2004）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
A case of preterm infant with 21-hydroxylase deficiency; the implication of the biochemical diagnosis by urinary pregnanetriolone using GCMS-SIM (gas chromatography mass spectrometry-selected ion monitoring).
- Author
- Hamajima T, Ohki S, Mizuno H, Homma K, Hasegawa T.
- Publication Title
- Magazine name Clin Pediatr Endocrinol Start Page 65-70 (Publication Date）2004）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
Elevated urine pregnanetriolone definitively establishes the diagnosis of classical 21-hydroxylase deficiency in term and preterm neonates.
- Author
- Homma K, Hasegawa T, Takeshita E, Watanabe K, Anzo M, Toyoura T, Jinno K, Ohashi T, Hamajima T, Takahashi Y, Takahashi T, Matsuo N.
- Publication Title
- Magazine name J Clin Endocrinol Metab Start Page 6087-6091 (Publication Date）2004）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
Genomic organization and sequence variation of the human integrin subunit 8 gene (ITGA8).
- Author
- Ekwa-Ekoba C, Diaz G, Carlson C, Hasegawa T, Lim K-c, Yabu J, Levy B, Schnapp LM.
- Publication Title
- Magazine name Matrix Biol Start Page 487-496 (Publication Date）2004）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
外性器異常を有し生後3週まで社会的性を決定されなかった1例
- Author
- 鈴木亜由子, 井ノ口美香子, 下郷幸子, 佐々木理恵, 堀尚明, 長谷川奉延, 高橋孝雄
- Publication Title
- Start Page 113-119 (Publication Date）2004）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- Without
先天性リポイド副腎過形成症の乳児の卵巣機能
- Author
- 上牧務, 長谷川奉延
- Publication Title
- Volume 52(Issue 増刊) Start Page 104−107 (Publication Date）2004）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- Without
Low birth weight slender bone group 低出生体重の細長い骨疾患グループ—概説
- Author
- 堀尚明, 長谷川奉延
- Publication Title
- Volume 36(Issue 増刊) Start Page 197−198 (Publication Date）2004）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- Without
Type II microcephalic osteodysplastic dysplasia 小頭性骨異形成異形成症II型
- Author
- 堀尚明, 長谷川奉延
- Publication Title
- Volume 36(Issue 増刊) Start Page 199−201 (Publication Date）2004）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- Without
Enchondromaatosis (Ollier) 内軟骨腫症 (Ollier病)
- Author
- 佐々木悟郎, 長谷川奉延
- Publication Title
- Volume 36(Issue 増刊) Start Page 257−259 (Publication Date）2004）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- Without
自己免疫性多腺性症候群
- Author
- 石井智弘, 長谷川奉延, 鈴木賀巳
- Publication Title
- Start Page 1550-1553 (Publication Date）2004）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- Without
Noonan症候群の遺伝的基盤
- Author
- 吉田理恵, 谷川奉延, 緒方勤
- Publication Title
- Start Page 1599-1604 (Publication Date）2004）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- Without
学校における神経性食欲不振症早期発見の試み
- Author
- 田中徹哉, 石井敬子, 廣金和枝, 佐藤明弘, 崔明順, 藤田尚代, 長谷川奉延, 徳村光昭, 川合志緒子, 南里清一郎, 木村慶子, 渡辺久子
- Publication Title
- Start Page 55-59 (Publication Date）2004）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- Without
先天性リポイド副腎過形成症の乳児の卵巣機能
- Author
- 上牧務, 長谷川奉延
- Publication Title
- Volume 52(Issue 増刊) Start Page 104−107 (Publication Date）2004）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- Without
Low birth weight slender bone group 低出生体重の細長い骨疾患グループ—概説
- Author
- 堀尚明, 長谷川奉延
- Publication Title
- Volume 36(Issue 増刊) Start Page 197−198 (Publication Date）2004）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- Without
Type II microcephalic osteodysplastic dysplasia 小頭性骨異形成異形成症II型
- Author
- 堀尚明, 長谷川奉延
- Publication Title
- Volume 36(Issue 増刊) Start Page 199−201 (Publication Date）2004）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- Without
Metaphyseal dysplasia Jansen type 骨幹端異形成症Jansen型
- Author
- 佐々木悟郎, 長谷川奉延
- Publication Title
- Volume 36(Issue 増刊) Start Page 374−375 (Publication Date）2004）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- Without
A new diagnostic test for very-long-chain acyl-CoA dehydrogenase deficiency using immunohistochemistry
- Author
- Ohashi Y, Hasegawa Y, Murayama K, Ogawa M, Hasegawa T, Kawai M, Sakata N, Yoshida K, Kamata H, Imai K, Kumagai I, Murakami K, Hasegawa H, Noguchi S, Nonaka I, Yamaguchi S, Nishino I.
- Publication Title
- Magazine name Neurology Volume 62(Issue 12) Start Page 2209-2213 (Publication Date）2004）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With
A newly recognized syndrome of metaphyseal undermodeling, spondylar dysplasia and overgrowth: report of three sporadic patients
- Author
- Nishimura G, Hasegawa T, Kinoshita E, Tanaka Y, Kurosawa K, Yoshimoto M.
- Publication Title
- Magazine name Am J Med Genet Volume 128A(Issue 2) Start Page 204-208 (Publication Date）2004）
- Authorship Category
- Joint Work
- Publication Category
- Research paper (scientific journal)
- Peer-review Status
- With