• 5756 Citations
  • 39 h-Index
1986 …2020

Research output per year

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Research Output

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Letter
2018

Responses to the letter to the editor “does growth-hormone treatment affect patients with and without a mitochondrial disorder differentially?” (Vol. 27, No. 2, p. 107-108, 2018)

Yokoya, S., Hasegawa, T., Ozono, K., Tanaka, H., Kanzaki, S., Tanaka, T., Chihara, K., Jia, N., Child, C. J., Ihara, K., Funai, J., Iwamoto, N. & Seino, Y., 2018 Jan 1, In : Clinical Pediatric Endocrinology. 27, 3, p. 201-202 2 p.

Research output: Contribution to journalLetter

2016

A novel dominant negative mutation in the intracellular domain of GHR is associated with growth hormone insensitivity

Takagi, M., Shinohara, H., Nagashima, Y., Hasegawa, Y., Narumi, S. & Hasegawa, T., 2016 Oct 1, In : Clinical Endocrinology. 85, 4, p. 669-671 3 p.

Research output: Contribution to journalLetter

3 Citations (Scopus)
2015

A case with neonatal hyperinsulinemic hypoglycemia: It is a characteristic complication of sotos syndrome

Nakamura, Y., Takagi, M., Yoshihashi, H., Miura, M., Narumi, S., Hasegawa, T., Miyake, Y. & Hasegawa, Y., 2015 May 1, In : American Journal of Medical Genetics, Part A. 167, 5, p. 1171-1174 4 p.

Research output: Contribution to journalLetter

8 Citations (Scopus)
2013

A recurrent mutation in the 5′-UTR of IFITM5 causes osteogenesis imperfecta type V

Takagi, M., Sato, S., Hara, K., Tani, C., Miyazaki, O., Nishimura, G. & Hasegawa, T., 2013 Aug 1, In : American Journal of Medical Genetics, Part A. 161, 8, p. 1980-1982 3 p.

Research output: Contribution to journalLetter

14 Citations (Scopus)

Spousal choice by height in an urban middle-class Japanese population

Uchida, K., Matsuo, N., Hori, N., Hasegawa, T. & Takahashi, T., 2013, In : Human Biology. 85, 4, p. 619-621 3 p.

Research output: Contribution to journalLetter

1 Citation (Scopus)
2012

A family of pseudohypoparathyroidism type Ia with an 850-kb submicroscopic deletion encompassing the whole GNAS locus

Mitsui, T., Nagasaki, K., Takagi, M., Narumi, S., Ishii, T. & Hasegawa, T., 2012 Jan 1, In : American Journal of Medical Genetics, Part A. 158 A, 1, p. 261-264 4 p.

Research output: Contribution to journalLetter

16 Citations (Scopus)

Atypical achondroplasia due to somatic mosaicism for the common thanatophoric dysplasia mutation R248C

Takagi, M., Kaneko-Schmitt, S., Suzumori, N., Nishimura, G. & Hasegawa, T., 2012 Jan 1, In : American Journal of Medical Genetics, Part A. 158 A, 1, p. 247-250 4 p.

Research output: Contribution to journalLetter

3 Citations (Scopus)

Mosaic upd(7)mat in a patient with Silver-Russell syndrome

Fuke-Sato, T., Yamazawa, K., Nakabayashi, K., Matsubara, K., Matsuoka, K., Hasegawa, T., Dobashi, K. & Ogata, T., 2012 Feb 1, In : American Journal of Medical Genetics, Part A. 158 A, 2, p. 465-468 4 p.

Research output: Contribution to journalLetter

5 Citations (Scopus)
2011

Prenatal diagnosis of osteogenesis imperfecta type II by three-dimensional ultrasound and computed tomography

Suzumori, N., Hasegawa, T. & Sugiura-Ogasawara, M., 2011 Jun 1, In : Journal of Obstetrics and Gynaecology Research. 37, 6, p. 664-665 2 p.

Research output: Contribution to journalLetter

2 Citations (Scopus)
2010

Late manifestations of tricho-rhino-pharangeal syndrome in a patient: Expanded skeletal phenotype in adulthood

Izumi, K., Takagi, M., Parikh, A. S., Hahn, A., Miskovsky, S. N., Nishimura, G., Torii, C., Kosaki, K., Hasegawa, T. & Neilson, D. E., 2010 Aug 1, In : American Journal of Medical Genetics, Part A. 152, 8, p. 2115-2119 5 p.

Research output: Contribution to journalLetter

6 Citations (Scopus)

Ruvalcaba syndrome revisited

Adachi, M., Muroya, K., Asakura, Y., Kurosawa, K., Nishimura, G., Narumi, S. & Hasegawa, T., 2010 Jul, In : American Journal of Medical Genetics, Part A. 152, 7, p. 1854-1857 4 p.

Research output: Contribution to journalLetter

1 Citation (Scopus)
2009

Mutation analysis of SOX9 and single copy number variant analysis of the upstream region in eight patients with campomelic dysplasia and acampomelic campomelic dysplasia

Wada, Y., Nishimura, G., Nagai, T., Sawai, H., Yoshikata, M., Miyagawa, S., Hanita, T., Sato, S., Hasegawa, T., Ishikawa, S. & Ogata, T., 2009 Dec 1, In : American Journal of Medical Genetics, Part A. 149, 12, p. 2882-2885 4 p.

Research output: Contribution to journalLetter

12 Citations (Scopus)
2007

Two distinctive mechanisms leading to disruption of the SHOX transcription unit in a single family

Izumi, K., Nakano, M., Kosaki, K., Kosaki, R., Hosogai, N., Matsumoto, H., Hasegawa, T., Takahashi, T. & Kosaki, K., 2007 Dec 1, In : American Journal of Medical Genetics, Part A. 143, 23, p. 2838-2842 5 p.

Research output: Contribution to journalLetter

2004

Hyperinsulinemic hypoglycemia in a newborn infant with trisomy 13 [1]

Tamame, T., Hori, N., Homma, H., Yoshida, R., Inokuchi, M., Kosaki, K., Takahashi, T. & Hasegawa, T., 2004 Sep 1, In : American Journal of Medical Genetics. 129 A, 3, p. 321-322 2 p.

Research output: Contribution to journalLetter

8 Citations (Scopus)

Two novel and one recurrent PTPN11 mutations in LEOPARD syndrome [1]

Ogata, T., Yoshida, R., Nagai, T., Hasegawa, T., Kinoshita, E. & Tanaka, T., 2004 Nov 1, In : American Journal of Medical Genetics. 130 A, 4, p. 432-434 3 p.

Research output: Contribution to journalLetter

24 Citations (Scopus)
2003

Microcephalic osteodysplastic primordial short stature type II with cafe-au-lait spots and moyamoya disease [2]

Nishimura, G., Hasegawa, T., Fujino, M., Hori, N. & Tomita, Y., 2003 Mar 15, In : American Journal of Medical Genetics. 117 A, 3, p. 299-301 3 p.

Research output: Contribution to journalLetter

20 Citations (Scopus)
1996

The transition from latent to overt hypoparathyroidism in a child with CATCH 22 who showed subnormal parathyroid hormone response to ethylenediamine tetraacetic acid infusion [3]

Hasegawa, T., Hasegawa, Y., Aso, T., Koto, S., Tanaka, N., Asamura, S., Nagai, T. & Tsuchiya, Y., 1996 Feb 13, In : European Journal of Pediatrics. 155, 3, 1 p.

Research output: Contribution to journalLetter

3 Citations (Scopus)

Transition from latent to overt hypoparathyroidism in a child with CATCH 22 [7]

Hasegawa, T., Hasegawa, Y., Aso, T., Koto, S., Tanaka, N., Asamura, S., Nagai, T. & Tsuchiya, Y., 1996 Jan 1, In : European Journal of Pediatrics. 155, 5, p. 425-426 2 p.

Research output: Contribution to journalLetter

1 Citation (Scopus)
1994

Diagnostic value of ethylenediaminetetraacetic acid infusion in partial DiGeorge anomaly

Crespo, M. F. R., Hasegawa, T., Hasegawa, Y. & Tsuchiya, Y., 1994 Oct 1, In : European Journal of Pediatrics. 153, 10, 1 p.

Research output: Contribution to journalLetter

1993
18 Citations (Scopus)
1992

Reply

Hasegawa, Y. & Hasegawa, T., 1992 Jan, In : The Journal of Pediatrics. 120, 1, 1 p.

Research output: Contribution to journalLetter