1-17 items (total 17)
Potential benefits of rapid genetic testing for germline WT1 in infants with bilateral renal tumors: A case report
- Author
- Yoshikawa H., Sato T., Ishikawa T., Ito J., Yamazaki F., Shima H., Honda M., Shibata H., Ishii T., Asanuma H., Shimada H., Hasegawa T.
- Publication Title
- Volume 69(Issue 2) (Publication Date）2022/02）
- ISSN
- 15455009
Potential usefulness of assessing serum betamethasone levels during betamethasone therapy
- Author
- Yano M., Sato T., Nakano S., Shimozato S., Ishii T., Hasegawa T.
- Publication Title
- (Publication Date）2023）
- ISSN
- 0334018X
Adapted whole-body surveillance for von Hippel–Lindau-associated tumors in 3p deletion syndrome with VHL deletion: A case report
- Author
- Morisawa K., Sato T., Shimoyamada M., Mizuno R., Ohashi H., Watanabe-Hisazumi H., Takeshima K., Kojima A., Sato S., Hasegawa T., Takahashi T.
- Publication Title
- Volume 69(Issue 11) (Publication Date）2022/11）
- ISSN
- 15455009
Cartilage-hair hypoplasia with T-cell dysfunction
- Author
- Tomomasa D., Sato T., Hasegawa T., Morio T., Kanegane H.
- Publication Title
- Volume 64(Issue 1) (Publication Date）2022/01）
- ISSN
- 13288067
Correction to: Growth references for Japanese individuals with Noonan syndrome (Pediatric Research, (2016), 79, 4, (543-548), 10.1038/pr.2015.254)
- Author
- Isojima T., Sakazume S., Hasegawa T., Ogata T., Nakanishi T., Nagai T., Yokoya S.
- Publication Title
- Volume 92(Issue 6) (Publication Date）2022/12）
- ISSN
- 00313998
Corrigendum: Validation of auxological reference values for Japanese children with Noonan syndrome and comparison with growth in children with Turner syndrome (Clin Pediatr Endocrinol, (2017) 26(3), (153-164), 10.1297/cpe.26.153)
- Author
- Isojima T., Sakazume S., Hasegawa T., Ogata T., Nakanishi T., Nagai T., Yokoya S.
- Publication Title
- Volume 31(Issue 3) (Publication Date）2022）
- ISSN
- 09185739
Effectiveness of dihydrotestosterone ointment on glans penis size increment in a 5-alpha-reductase type 2 deficiency patient
- Author
- Sato T., Nakano S., Asanuma H., Ishii T., Hasegawa T.
- Publication Title
- Volume 64(Issue 1) (Publication Date）2022/01）
- ISSN
- 13288067
Gonadotropin-dependent precocious puberty in a female offspring who is a potential carrier for BRCA2 pathogenic variant: An additional consideration for gonadotropin-releasing hormone agonist treatment
- Author
- Tsuura K., Sato T., Nakano S., Ishii T., Hasegawa T.
- Publication Title
- Volume 70(Issue 6) (Publication Date）2023/06）
- ISSN
- 15455009
One microliter of blood for SRY testing in a neonate with atypical genitalia
- Author
- Mizuno Y., Sato T., Shimura K., Ishii T., Hasegawa T.
- Publication Title
- Volume 64(Issue 1) (Publication Date）2022/01）
- ISSN
- 13288067
Parathyroid adenoma with a somatic CASR pathogenic variant: A pediatric case report
- Author
- Kawata K., Sato T., Honda M., Narumi S., Kameyama K., Ishii T., Hasegawa T.
- Publication Title
- Volume 70(Issue 12) (Publication Date）2023/12）
- ISSN
- 15455009
特集 小児の負荷試験2019 総説 医療安全対策(リスクマネージメント)からみた小児の負荷試験
- Author
- 水野 裕介, 長谷川 奉延
- Publication Title
- Volume 51(Issue 4) Start Page 417 - End Page 417 (Publication Date）2019/04）
日本小児内分泌学会推薦総説 先天性甲状腺機能低下症の分子遺伝学
- Author
- 鳴海 覚志, 長谷川 奉延
- Publication Title
- Magazine name The journal of the Japan Pediatric Society Volume 118(Issue 10) Start Page 1450 - End Page 1456 (Publication Date）2014/10）
Ultrasound finding of vaginal bleeding in infants with 21-hydroxylase deficiency
- Author
- Sato T., Ishii T., Ichihashi Y., Asanuma H., Hasegawa T.
- Publication Title
- Volume 64(Issue 1) (Publication Date）2022/01）
- ISSN
- 13288067
A novel missense variant of FGFR1 in a Japanese girl with Kallmann syndrome and holoprosencephaly
- Author
- Uchida N., Mizuno Y., Seno S., Koyama Y., Takahashi T., Shibata H., Narumi S., Hasegawa T., Ishii T.
- Publication Title
- Volume 32(Issue 1) Start Page 79 - End Page 81 (Publication Date）2023）
- ISSN
- 09185739
A novel SOX2 frameshift pathogenic variant located in the transactivation domain in a male infant with hypogonadotropic hypogonadism
- Author
- Kimura-Yoshida A., Sato T., Ichihashi Y., Wasa M., Narumi S., Ishii T., Hasegawa T.
- Publication Title
- Volume 33(Issue 4) Start Page 244 - End Page 248 (Publication Date）2024）
- ISSN
- 09185739
Clinical and Immunological Analyses of Ten Patients with MIRAGE Syndrome
- Author
- Mitsui-Sekinaka K., Narumi S., Sekinaka Y., Uematsu K., Yoshida Y., Amano N., Shima H., Hasegawa T., Nonoyama S.
- Publication Title
- Volume 41(Issue 3) Start Page 709 - End Page 711 (Publication Date）2021/04）
- ISSN
- 02719142
Response to Letter to the Editor From Janot et al: “Single-Exon Deletions of ZNRF3 Exon 2 Cause Congenital Adrenal Hypoplasia”
- Author
- Amano N., Narumi S., Ishii T., Hasegawa T.
- Publication Title
- Volume 109(Issue 9) (Publication Date）2024/09）
- ISSN
- 0021972X