Sutani A - Search Results

1

WDR11 is another causative gene for coloboma, cardiac anomaly and growth retardation in 10q26 deletion syndrome.

Sutani A, Shima H, Hijikata A, Hosokawa S, Katoh-Fukui Y, Takasawa K, Suzuki E, Doi S, Shirai T, Morio T, Fukami M, Kashimada K. Sutani A, et al. Eur J Med Genet. 2020 Jan;63(1):103626. doi: 10.1016/j.ejmg.2019.01.016. Epub 2019 Jan 31. Eur J Med Genet. 2020. PMID: 30711679

2

Total body irradiation for hematopoietic stem cell transplantation during early childhood is associated with the risk for diabetes mellitus.

Nakagawa R, Hosokawa-Tsuji A, Aoki Y, Takasawa K, Maru M, Nakajima K, Sutani A, Miyakawa Y, Tomizawa D, Kashimada K, Morio T. Nakagawa R, et al. Among authors: sutani a. Endocrine. 2018 Jul;61(1):76-82. doi: 10.1007/s12020-018-1595-3. Epub 2018 Apr 24. Endocrine. 2018. PMID: 29691808

3

Gonadal failure among female patients after hematopoietic stem cell transplantation for non-malignant diseases.

Sutani A, Miyakawa Y, Tsuji-Hosokawa A, Nomura R, Nakagawa R, Nakajima K, Maru M, Aoki Y, Takasawa K, Takagi M, Imai K, Kashimada K, Morio T. Sutani A, et al. Clin Pediatr Endocrinol. 2019;28(4):105-112. doi: 10.1297/cpe.28.105. Epub 2019 Oct 19. Clin Pediatr Endocrinol. 2019. PMID: 31666763 Free PMC article.

4

In vitro generation of functional murine heart organoids via FGF4 and extracellular matrix.

Lee J, Sutani A, Kaneko R, Takeuchi J, Sasano T, Kohda T, Ihara K, Takahashi K, Yamazoe M, Morio T, Furukawa T, Ishino F. Lee J, et al. Among authors: sutani a. Nat Commun. 2020 Sep 3;11(1):4283. doi: 10.1038/s41467-020-18031-5. Nat Commun. 2020. PMID: 32883967 Free PMC article.

5

The progression of salt-wasting and the body weight change during the first 2 weeks of life in classical 21-hydroxylase deficiency patients.

Gau M, Konishi K, Takasawa K, Nakagawa R, Tsuji-Hosokawa A, Hashimoto A, Sutani A, Tajima T, Hasegawa T, Morio T, Kashimada K. Gau M, et al. Among authors: sutani a. Clin Endocrinol (Oxf). 2021 Feb;94(2):229-236. doi: 10.1111/cen.14347. Epub 2020 Oct 20. Clin Endocrinol (Oxf). 2021. PMID: 33001476

6

Marked clinical heterogeneity in congenital hyperinsulinism due to a novel homozygous ABCC8 mutation.

Takasawa K, Miyakawa Y, Saito Y, Adachi E, Shidei T, Sutani A, Gau M, Nakagawa R, Taki A, Kashimada K, Morio T. Takasawa K, et al. Among authors: sutani a. Clin Endocrinol (Oxf). 2021 Jun;94(6):940-948. doi: 10.1111/cen.14443. Epub 2021 Mar 14. Clin Endocrinol (Oxf). 2021. PMID: 33595839

7

Adrenal suppression and anthropometric data at two years of age was not influenced by the initial hydrocortisone dose in patients with 21-hydroxylase deficiency.

Saito Y, Takasawa K, Gau M, Yamauchi T, Nakagawa R, Miyakawa Y, Sutani A, Hosokawa-Tsuji A, Takishima S, Matsubara Y, Morio T, Kashimada K. Saito Y, et al. Among authors: sutani a. Clin Pediatr Endocrinol. 2021;30(4):155-161. doi: 10.1297/cpe.30.155. Epub 2021 Oct 1. Clin Pediatr Endocrinol. 2021. PMID: 34629737 Free PMC article.

8

Autonomously functioning thyroid nodule due to a somatic TSHR mutation.

Iemura R, Kirino S, Sutani A, Kashimada K, Takasawa K. Iemura R, et al. Among authors: sutani a. Pediatr Int. 2022 Jan;64(1):e15157. doi: 10.1111/ped.15157. Pediatr Int. 2022. PMID: 35998123 No abstract available.

9

The High Relevance of 21-Deoxycortisol, (Androstenedione + 17α-Hydroxyprogesterone)/Cortisol, and 11-Deoxycortisol/17α-Hydroxyprogesterone for Newborn Screening of 21-Hydroxylase Deficiency.

Watanabe K, Tsuji-Hosokawa A, Hashimoto A, Konishi K, Ishige N, Yajima H, Sutani A, Nakatani H, Gau M, Takasawa K, Tajima T, Hasegawa T, Morio T, Kashimada K. Watanabe K, et al. Among authors: sutani a. J Clin Endocrinol Metab. 2022 Nov 25;107(12):3341-3352. doi: 10.1210/clinem/dgac521. J Clin Endocrinol Metab. 2022. PMID: 36071550

10

A novel SLC5A2 heterozygous variant in a family with familial renal glucosuria.

Hatano M, Udagawa T, Kanamori T, Sutani A, Mori T, Sohara E, Uchida S, Morio T, Nishioka M. Hatano M, et al. Among authors: sutani a. Hum Genome Var. 2022 Dec 1;9(1):42. doi: 10.1038/s41439-022-00221-w. Hum Genome Var. 2022. PMID: 36450716 Free PMC article.

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