Sawano K - Search Results

1

A Japanese family with a heterozygous novel mutation in the Indian hedgehog gene exhibiting a broad spectrum of clinical features and radiological findings.

Onuki T, Shibata N, Hiroshima S, Sawano K, Nagasaki K. Onuki T, et al. Among authors: sawano k. Congenit Anom (Kyoto). 2022 Jan;62(1):47-48. doi: 10.1111/cga.12445. Epub 2021 Oct 12. Congenit Anom (Kyoto). 2022. PMID: 34591992 No abstract available.

2

Timing of hyponatremia development in patients with salt-wasting-type 21-hydroxylase deficiency.

Shima R, Sawano K, Shibata N, Nyuzuki H, Sasaki S, Sato H, Ogawa Y, Abe Y, Nagasaki K, Saitoh A. Shima R, et al. Among authors: sawano k. Clin Pediatr Endocrinol. 2020;29(3):105-110. doi: 10.1297/cpe.29.105. Epub 2020 Jul 11. Clin Pediatr Endocrinol. 2020. PMID: 32694886 Free PMC article.

3

Letter to the Editor: Testosterone priming increased growth hormone peak levels in the stimulation test and suppressed gonadotropin secretion in three Japanese adolescent boys.

Sawano K, Nagasaki K. Sawano K, et al. Clin Pediatr Endocrinol. 2020;29(4):201. doi: 10.1297/cpe.29.201. Epub 2020 Oct 3. Clin Pediatr Endocrinol. 2020. PMID: 33088021 Free PMC article. No abstract available.

4

Re-Evaluation of the Prevalence of Permanent Congenital Hypothyroidism in Niigata, Japan: A Retrospective Study.

Nagasaki K, Sato H, Sasaki S, Nyuzuki H, Shibata N, Sawano K, Hiroshima S, Asami T. Nagasaki K, et al. Among authors: sawano k. Int J Neonatal Screen. 2021 May 28;7(2):27. doi: 10.3390/ijns7020027. Int J Neonatal Screen. 2021. PMID: 34071177 Free PMC article.

5

Two cases of cytochrome P450 oxidoreductase deficiency with severe scoliosis and surgery requirement.

Onuki T, Ohtsu Y, Hiroshima S, Sawano K, Nagasaki K. Onuki T, et al. Among authors: sawano k. Congenit Anom (Kyoto). 2021 Sep;61(5):202-203. doi: 10.1111/cga.12434. Epub 2021 Jun 29. Congenit Anom (Kyoto). 2021. PMID: 34155696 No abstract available.

6

A case of adolescent trichorhinophalangeal syndrome undergoing pelvic osteotomy for bilateral acetabular dysplasia.

Sawano K, Nyuzuki H, Nagasaki K, Suzuki H, Suda K, Miyasaka D, Imai N, Saitoh A. Sawano K, et al. J Orthop Sci. 2023 Nov;28(6):1501-1504. doi: 10.1016/j.jos.2021.07.021. Epub 2021 Sep 6. J Orthop Sci. 2023. PMID: 34503898 No abstract available.

7

Carotenoderma with hypothyroidism.

Sawano K, Nagasaki K. Sawano K, et al. Arch Dis Child. 2022 Jun;107(6):615. doi: 10.1136/archdischild-2021-323051. Epub 2021 Nov 12. Arch Dis Child. 2022. PMID: 34772661 No abstract available.

8

A 7-year-old boy with central diabetes insipidus presenting with thickened pituitary stalk and anti-rabphilin-3A antibody positivity.

Morota K, Tadokoro H, Sawano K, Watanabe K, Iwata N, Fujisawa H, Suzuki A, Sugimura Y, Nagasaki K. Morota K, et al. Among authors: sawano k. J Pediatr Endocrinol Metab. 2022 Feb 4;35(5):687-690. doi: 10.1515/jpem-2021-0674. Print 2022 May 25. J Pediatr Endocrinol Metab. 2022. PMID: 35119230

9

Expanding the phenotypic spectrum of ARCN1-related syndrome.

Ritter AL, Gold J, Hayashi H, Ackermann AM, Hanke S, Skraban C, Cuddapah S, Bhoj E, Li D, Kuroda Y, Wen J, Takeda R, Bibb A, El Chehadeh S, Piton A, Ohl J, Kukolich MK, Nagasaki K, Kato K, Ogi T, Bhatti T, Russo P, Krock B, Murrell JR, Sullivan JA, Shashi V, Stong N, Hakonarson H, Sawano K, Torti E, Willaert R, Si Y, Wilcox WR, Wirgenes KV, Thomassen K, Carlotti K, Erwin A, Lazier J, Marquardt T, He M, Edmondson AC, Izumi K. Ritter AL, et al. Among authors: sawano k. Genet Med. 2022 Jun;24(6):1227-1237. doi: 10.1016/j.gim.2022.02.005. Epub 2022 Mar 14. Genet Med. 2022. PMID: 35300924 Free PMC article.

10

Asymmetrical Graves' disease in children: potential usefulness of potassium iodide monotherapy.

Fukahori K, Sawano K, Yoshida H, Nagasaki K. Fukahori K, et al. Among authors: sawano k. BMJ Case Rep. 2022 Apr 22;15(4):e249571. doi: 10.1136/bcr-2022-249571. BMJ Case Rep. 2022. PMID: 35459658 Free PMC article.

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