Nakajima H - Search Results

1

An infantile case of pseudohypoaldosteronism type 1 (PHA1) caused by a novel mutation of NR3C2.

Goda T, Komatsu H, Nozu K, Nakajima H. Goda T, et al. Among authors: nakajima h. Clin Pediatr Endocrinol. 2020;29(3):127-130. doi: 10.1297/cpe.29.127. Epub 2020 Jul 11. Clin Pediatr Endocrinol. 2020. PMID: 32694891 Free PMC article. No abstract available.

2

Decrement in bone mineral density after parathyroidectomy in a pediatric patient with primary hyperparathyroidism.

Morimoto H, Nakajima H, Mori J, Fukuhara S, Shigehara K, Adachi S, Hosoi H. Morimoto H, et al. Among authors: nakajima h. Clin Pediatr Endocrinol. 2018;27(2):81-86. doi: 10.1297/cpe.27.81. Epub 2018 Apr 13. Clin Pediatr Endocrinol. 2018. PMID: 29662267 Free PMC article.

3

A case of pseudohypoparathyroidism type Ia with a novel frameshift mutation in the GNAS gene: early diagnosis of osteoma cutis by skin biopsy.

Kodo K, Maeda H, Morimoto H, Wada M, Imura T, Nakajima H. Kodo K, et al. Among authors: nakajima h. Clin Pediatr Endocrinol. 2019;28(1):15-18. doi: 10.1297/cpe.28.15. Epub 2019 Jan 31. Clin Pediatr Endocrinol. 2019. PMID: 30745729 Free PMC article. No abstract available.

4

A pediatric case of hypomagnesemia 1 (HOMG1) caused by novel compound heterozygous mutations in TRPM6.

Goda T, Komatsu H, Nozu K, Nakajima H. Goda T, et al. Among authors: nakajima h. Hum Genome Var. 2019 Mar 6;6:13. doi: 10.1038/s41439-019-0043-0. eCollection 2019. Hum Genome Var. 2019. PMID: 30911400 Free PMC article.

5

Klinefelter syndrome in an adolescent with severe obesity, insulin resistance, and hyperlipidemia, successfully treated with testosterone replacement therapy.

Fukuhara S, Mori J, Nakajima H. Fukuhara S, et al. Among authors: nakajima h. Clin Pediatr Endocrinol. 2021;30(3):127-132. doi: 10.1297/cpe.30.127. Epub 2021 Jul 10. Clin Pediatr Endocrinol. 2021. PMID: 34285454 Free PMC article.

6

Two Japanese siblings with arginase-1 deficiency identified using a novel frameshift mutation of ARG1 (p.Lys41Thrfs^∗2).

Nakajima H, Fukuhara S. Nakajima H, et al. J Pediatr Endocrinol Metab. 2021 Oct 18;35(1):125-129. doi: 10.1515/jpem-2021-0436. Print 2022 Jan 27. J Pediatr Endocrinol Metab. 2021. PMID: 34653322

7

Traumatic herniation of the buccal fat pad.

Iehara T, Tomoyasu C, Nakajima H, Osamura T, Hosoi H. Iehara T, et al. Among authors: nakajima h. Pediatr Int. 2016 Jul;58(7):613-5. doi: 10.1111/ped.12852. Epub 2016 Feb 19. Pediatr Int. 2016. PMID: 26892590

8

Arterial stiffness in junior high school students: Longitudinal observations.

Fujiwara H, Nakajima H, Inoue F, Kosaka K, Asano H, Yoshii K. Fujiwara H, et al. Among authors: nakajima h. Pediatr Int. 2018 Feb;60(2):127-135. doi: 10.1111/ped.13475. Pediatr Int. 2018. PMID: 29230906

9

A Case of Infantile Alagille Syndrome With Severe Dyslipidemia: New Insight into Lipid Metabolism and Therapeutics.

Nakajima H, Tsuma Y, Fukuhara S, Kodo K. Nakajima H, et al. J Endocr Soc. 2022 Jan 18;6(3):bvac005. doi: 10.1210/jendso/bvac005. eCollection 2022 Mar 1. J Endocr Soc. 2022. PMID: 35155971 Free PMC article.

10

Association of Type 2 Deiodinase Thr92Ala Polymorphism with Pediatric Obesity in Japanese Children: A Case-Control Study.

Ota T, Mori J, Kawabe Y, Morimoto H, Fukuhara S, Kodo K, Sugimoto S, Kosaka K, Nakajima H, Hosoi H. Ota T, et al. Among authors: nakajima h. Children (Basel). 2022 Sep 20;9(10):1421. doi: 10.3390/children9101421. Children (Basel). 2022. PMID: 36291357 Free PMC article.

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