Papers - Hasegawa, Tomonobu
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Prenatal diagnosis of osteogenesis imperfect type II by three-dimensional ultrasound and computed tomography.
Suzumori N, Hasegawa T, Sugiura-Ogasawara M
J Obstet Gynaecol Res 37 664 - 665 2011
Joint Work
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Molecular Basis of Thyroid Dyshormonogenesis: Genetic Screening in Population-Based Japanese Patients.
Narumi S, Muroya K, Asakura Y, Adachi M, Hasegawa T
J Clin Endicrinol Metab 96 E1838 - 1842 2011
Joint Work
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BMI z-score is the optimal measure of annual adiposity change in elementary children.
Inokuchi M, Matsuo N, Takayama JI, Hasegawa T
Ann Hum Biol 38 747 - 751 2011
Joint Work
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PAX8 mutation disturbing thyroid follicular growth: A case report.
Narumi S, Yoshida A, Muroya K, Asakura Y, Adachi M, Fukuzawa R, Kameyama K, Hasegawa T
J Clin Endocrinol Metab 96 E2039 - 2044 2011
Joint Work
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成長ホルモン分泌不全性低身長症における成長ホルモン前思春期の治療開始年齢別治療効果
8. 田中敏章、伊藤純子、神崎晋、島津章、田中弘之、寺本明、永井敏郎、長谷川奉延、羽二生邦彦、藤田敬之助、堀川玲子、向井徳男、和田尚弘、横谷進
日本成長学会雑誌 16 23 - 29 2010
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Various types of LRP5 mutations in four patients with osteoporosis-pseudoglioma syndrome: Identification of a7.2-kb microdeletion using oligonucleotide tiling microarray
Narumi S, Numakura C, Shiihara Takashi, Seiwa C, Nozaki Y, Momoi M, Watanabe Y, Yoshino M, Matsuishi T, Nishi E, Kawame H, Akahane T, Nishimura G, Emi Mitsuru, Hasegawa T
Am J Med Genet 152A 133-140 2010
Research paper (scientific journal), Joint Work
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The effect of intramuscular testosterone enanthate treatment on stretched penile length in prepubertal boys with hypospadias
Ishii T, Hayashi M, Suwanai A, Amano N, Hasegawa T
J Urol 76 97-100 2010
Research paper (scientific journal), Joint Work
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Transcription-factor mutations and congenital hypothyroidism: Systematic genetic screening of a population-based cohort of Japanese patients
Narumi S, Muroya K, Asakura Y, Adachi M, Hasegawa T
J Clin Endocrinol Metab 95 1981-1985 2010
Research paper (scientific journal), Joint Work
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Unilateral adrenalectomy can be an alternative therapy for infantile onset Cushing’s syndrome caused by ACTH-independent macronodular adrenal hyperplasia with McCune-Albright syndrome
Hamajima T, Maruwaka K, Homma K, Matsuo K, Fujieda K, Hasegawa T
Endocrine J 57 819-824 2010
Research paper (scientific journal), Joint Work
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Progression of Goiter in Pendred Syndrome is Associated with Increase of Thyroidal Iodine Uptake but not with Iodine Organification Defect: Report of a Patient with SLC26A4 Mutations
Asakura Y, Narumi S, Muroya K, Fujita K, Aida N, Hasegawa T, Adachi M
Am J Med Genet 152A 1793-1997 2010
Research paper (scientific journal), Joint Work
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One novel and two recurrent THRB mutations associated with resistance to thyroid hormone: Structure-based computational mutation prediction
Narumi S, Cho H, Tamada I, Kozu Y, Tsuchiya T, Nagai T, Hasegawa T
Clin pediatr Endocrinolo 19 91-99 2010
Research paper (scientific journal), Joint Work
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Ruvalcaba syndrome revisited
Adachi M, Muroya K, Asakura Y, Kurosawa K, Nishimura G, Narumi S, Hasegawa T
Am J Med Genet 152A 1854-1857 2010
Research paper (scientific journal), Joint Work
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Late manifestations of Tricho-Rhino-Pharangeal syndrome in a patient: Expanded skeletal phenotype in adulthood
Izumi K, Takagi M, Parikh A, Hahn A, Miskovsky SN, Nishimura G, Torii C, Kosaki K, Hasegawa T, Neilson DE.
Am J Med Genet 152(A) 2115-2119 2010
Research paper (scientific journal), Joint Work
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小児期メタボリックシンドロームの早期診断とその意義
井ノ口美香子、長谷川奉延
小児科診療 73 277 - 282 2010
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思春期における性分化疾患の治療とカウンセリング
天野直子、長谷川奉延
産婦人科の実際 59 447 - 452 2010
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アンドロゲン不応症
天野直子、長谷川奉延
産科と婦人科 77 1283 - 1287 2010
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家族性先天性甲状腺機能低下症の臨床的・分子遺伝学的検討
長崎啓祐、鳴海覚志、浅見直、小川洋平、菊池透、長谷川奉延、内山聖
ホと臨床 57 1001 - 1005 2010
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尿中遊離型ベタメサゾンGC/MS測定法の確立と母体投与早産児尿中遊離型ベタメサゾン分析 ホと臨床 57 1013-1015 (2010)
小山雄平、本間桂子、三輪雅之、丹羽房子、河井昌彦、村田満、池田一成、長谷川奉延
ホと臨床 57 1013 - 1015 2010
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日本における21-水酸化酵素欠損症の出生前診断・治療の現状調査
田島敏広、長谷川奉延、小川英伸、堀川玲子、木下英一、原田正平、猪股弘明、安達昌功、西美和、楠田聡、大関武彦、藤枝憲二
ホと臨床 57 1021 - 1023 2010
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SF-1, DAX-1と小児内分泌疾患
佐々木悟郎、長谷川奉延
ホと臨床 58 157 - 162 2010