年別の研究成果
年別の研究成果
- 19 件
検索結果
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2022
Adapted whole-body surveillance for von Hippel–Lindau-associated tumors in 3p deletion syndrome with VHL deletion: A case report
Morisawa, K., Sato, T., Shimoyamada, M., Mizuno, R., Ohashi, H., Watanabe-Hisazumi, H., Takeshima, K., Kojima, A., Sato, S., Hasegawa, T. & Takahashi, T., 2022, (Accepted/In press) In: Pediatric Blood and Cancer.研究成果: Letter › 査読
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2021
Pertussis Epidemic in Lower-Grade Schoolchildren Without Preschool Vaccination Boosters
Kimiya, T., Shinjoh, M., Miyata, A. & Takahashi, T., 2021 1月 15, In: Indian Pediatrics. 58, 1, p. 73-74 2 p.研究成果: Letter › 査読
1 被引用数 (Scopus) -
Research Letters
Bandi, R., Lathiya, R., Lingappa, L., Konanki, R., Kimiya, T., Shinjoh, M., Miyata, A., Takahashi, T., Shah, S., Kaul, A., Shah, R. & Maddipoti, S., 2021 1月, In: Indian Pediatrics. 58, 1, p. 71-76 6 p.研究成果: Letter › 査読
Open Access1 被引用数 (Scopus) -
2018
Spontaneous intramural duodenal hematoma as the manifestation of Noonan syndrome
Yamazawa, K., Yamada, Y., Kuroda, T., Mutai, H., Matsunaga, T., Komiyama, O. & Takahashi, T., 2018 2月, In: American Journal of Medical Genetics, Part A. 176, 2, p. 496-498 3 p.研究成果: Letter › 査読
1 被引用数 (Scopus) -
2017
Co-occurrence of Sturge–Weber syndrome and Klippel–Trenaunay–Weber syndrome phenotype: Consideration of the historical aspect
Sakaguchi, Y., Takenouchi, T., Uehara, T., Kishi, K., Takahashi, T. & Kosaki, K., 2017 10月, In: American Journal of Medical Genetics, Part A. 173, 10, p. 2831-2833 3 p.研究成果: Letter › 査読
4 被引用数 (Scopus) -
Successful haploidentical BMT with post-transplant cyclophosphamide for refractory autoimmune pancytopenia after cord blood transplant in pediatric myelodysplastic syndrome
Shima, H., Isshiki, K., Yamada, Y., Yamazaki, F., Takahashi, T. & Shimada, H., 2017 4月 1, In: Bone Marrow Transplantation. 52, 4, p. 653-655 3 p.研究成果: Letter › 査読
Open Access1 被引用数 (Scopus) -
2013
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.研究成果: Letter › 査読
1 被引用数 (Scopus) -
2012
Imatinib is effective for prevention and improvement of fibrotic fasciitis as a manifestation of chronic GVHD
Osumi, T., Miharu, M., Tanaka, R., Du, W., Takahashi, T. & Shimada, H., 2012 1月, In: Bone Marrow Transplantation. 47, 1, p. 139-140 2 p.研究成果: Letter › 査読
9 被引用数 (Scopus) -
2010
Interstitial microdeletion of 4p16.3: Contribution of WHSC1 haploinsufficiency to the pathogenesis of developmental delay in Wolf-Hirschhorn syndrome
Izumi, K., Okuno, H., Maeyama, K., Sato, S., Yamamoto, T., Torii, C., Kosaki, R., Takahashi, T. & Kosaki, K., 2010 4月 1, In: American Journal of Medical Genetics, Part A. 152, 4, p. 1028-1032 5 p.研究成果: Letter › 査読
14 被引用数 (Scopus) -
Transverse limb defect in a patient with Jacobsen syndrome: Concurrence of malformation and disruption
Fujita, H., Yanagi, T., Kosaki, R., Torii, C., Bamba, M., Takahashi, T. & Kosaki, K., 2010 4月, In: American Journal of Medical Genetics, Part A. 152, 4, p. 1033-1035 3 p.研究成果: Letter › 査読
9 被引用数 (Scopus) -
2008
Split hand foot malformation with whorl-like pigmentary pattern: Phenotypic expression of somatic mosaicism for the p63 mutation
Kosaki, R., Naito, Y., Torii, C., Takahashi, T., Nakajima, T. & Kosaki, K., 2008 10月 1, In: American Journal of Medical Genetics, Part A. 146, 19, p. 2574-2577 4 p.研究成果: Letter › 査読
10 被引用数 (Scopus) -
Tietz syndrome: Unique phenotype specific to mutations of MITF nuclear localization signal
Izumi, T., Kohta, A., Kimura, Y., Ishida, S., Takahashi, T., Ishiko, A. & Kosaki, K., 2008 7月 1, In: Clinical Genetics. 74, 1, p. 93-95 3 p.研究成果: Letter › 査読
28 被引用数 (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 12月 1, In: American Journal of Medical Genetics, Part A. 143, 23, p. 2838-2842 5 p.研究成果: Letter › 査読
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2006
Cleidocranial dysplasia plus vascular anomalies with 6p21.2 microdeletion spanning RUNX2 and VEGF [4]
Izumi, K., Yahagi, N., Fujii, Y., Higuchi, M., Kosaki, R., Naito, Y., Nishimura, G., Hosokai, N., Takahashi, T. & Kosaki, K., 2006 2月 15, In: American Journal of Medical Genetics. 140 A, 4, p. 398-401 4 p.研究成果: Letter › 査読
18 被引用数 (Scopus) -
Molecular pathology of Shprintzen-Goldberg syndrome [4]
Kosaki, K., Takahashi, D., Udaka, T., Kosaki, R., Matsumoto, M., Ibe, S., Isobe, T., Tanaka, Y. & Takahashi, T., 2006 1月 1, In: American Journal of Medical Genetics. 140 A, 1, p. 104-108 5 p.研究成果: Letter › 査読
62 被引用数 (Scopus) -
2005
Iridic and retinal coloboma associated with prenatal methimazole exposure [1]
Aramaki, M., Hokuto, I., Matsumoto, T., Ishimoto, H., Inoue, M., Kimura, T., Oikawa, Y. I., Ikeda, K., Yoshimura, Y., Takahashi, T. & Kosaki, K., 2005, In: American Journal of Medical Genetics, Part A. 139 A, 2, p. 156-158 3 p.研究成果: Letter › 査読
18 被引用数 (Scopus) -
Little response to zoledronic acid in a child of juvenile myelomonocytic leukemia (JMML) harboring the PTPN11 mutation [2]
Shimada, H., Shima, H., Shimasaki, N., Yoshihara, H., Mori, T. & Takahashi, T., 2005 8月, In: Annals of Oncology. 16, 8, p. 1400 1 p.研究成果: Letter › 査読
10 被引用数 (Scopus) -
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 9月 1, In: American Journal of Medical Genetics. 129 A, 3, p. 321-322 2 p.研究成果: Letter › 査読
12 被引用数 (Scopus) -
Somatic PTPN11 mutation with a heterogenous clonal origin in children with juvenile myelomonocytic leukemia [3]
Shimada, H., Mori, T., Shimasaki, N., Shimizu, K., Takahashi, T. & Kosaki, K., 2004 6月, In: Leukemia. 18, 6, p. 1142-1144 3 p.研究成果: Letter › 査読
9 被引用数 (Scopus)