Mukai T - Search Results

1

Glycemic control and motor development in a patient with intermediate DEND.

Oka H, Suzuki S, Furuya A, Matsuo K, Amamiya S, Oshima M, Oka T, Mukai T, Okayama A, Araki A, Azuma H, Tanahashi Y. Oka H, et al. Among authors: mukai t. Pediatr Int. 2014 Jun;56(3):432-5. doi: 10.1111/ped.12294. Pediatr Int. 2014. PMID: 24894933

2

Molecular basis of neonatal diabetes in Japanese patients.

Suzuki S, Makita Y, Mukai T, Matsuo K, Ueda O, Fujieda K. Suzuki S, et al. Among authors: mukai t. J Clin Endocrinol Metab. 2007 Oct;92(10):3979-85. doi: 10.1210/jc.2007-0486. Epub 2007 Jul 17. J Clin Endocrinol Metab. 2007. PMID: 17635943

3

Prevalence and risk factors of vitamin D deficiency rickets in Hokkaido, Japan.

Matsuo K, Mukai T, Suzuki S, Fujieda K. Matsuo K, et al. Among authors: mukai t. Pediatr Int. 2009 Aug;51(4):559-62. doi: 10.1111/j.1442-200X.2009.02834.x. Epub 2009 Mar 27. Pediatr Int. 2009. PMID: 19419526

4

A Case of Vitamin D Deficiency without Elevation of Serum Alkaline Phosphatase in a Carrier of Hypophosphatasia.

Matsuo K, Mukai T, Furuya A, Suzuki S, Tanahashi Y, Azuma H. Matsuo K, et al. Among authors: mukai t. Clin Pediatr Endocrinol. 2013 Oct;22(4):73-6. doi: 10.1292/cpe.22.73. Epub 2013 Oct 26. Clin Pediatr Endocrinol. 2013. PMID: 24170964 Free PMC article.

5

Sufficient increment of sulfonylurea without reintroduction of insulin ameliorates pubertal deterioration of glycaemic control in KCNJ11 neonatal diabetes treated with long-term sulfonylurea.

Suzuki S, Mukai T, Kokumai T, Furuya A, Tanahashi Y, Azuma H. Suzuki S, et al. Among authors: mukai t. Diabetologia. 2020 Aug;63(8):1659-1661. doi: 10.1007/s00125-020-05182-9. Epub 2020 May 24. Diabetologia. 2020. PMID: 32448915 No abstract available.

6

Non-invasive discrimination of acute focal bacterial nephritis with pyelonephritis.

Oka H, Nagamori T, Yamamoto S, Manabe H, Taketazu G, Mukai T, Sakata H, Oki J. Oka H, et al. Among authors: mukai t. Pediatr Int. 2019 Aug;61(8):777-780. doi: 10.1111/ped.13910. Epub 2019 Aug 14. Pediatr Int. 2019. PMID: 31410918

7

A 34-year-old Japanese patient exhibiting NBAS deficiency with a novel mutation and extended phenotypic variation.

Suzuki S, Kokumai T, Furuya A, Nagamori T, Matsuo K, Ueda O, Mukai T, Ito Y, Yano K, Fujieda K, Okuno A, Tanahashi Y, Azuma H. Suzuki S, et al. Among authors: mukai t. Eur J Med Genet. 2020 Nov;63(11):104039. doi: 10.1016/j.ejmg.2020.104039. Epub 2020 Aug 14. Eur J Med Genet. 2020. PMID: 32805445

8

A mutation of the β-domain in POU1F1 causes pituitary deficiency due to dominant PIT-1β expression.

Suzuki S, Matsuo K, Ito Y, Kobayashi A, Kokumai T, Furuya A, Ueda O, Mukai T, Yano K, Fujieda K, Okuno A, Tanahashi Y, Azuma H. Suzuki S, et al. Among authors: mukai t. Eur J Endocrinol. 2021 May 21;185(1):1-12. doi: 10.1530/EJE-20-1313. Eur J Endocrinol. 2021. PMID: 33886498

9

Early Diagnosis of Wolfram Syndrome by Ophthalmologic Screening in a Patient with Type 1B Diabetes Mellitus: A Case Report.

Kokumai T, Suzuki S, Nishikawa N, Yamamura H, Mukai T, Tanahashi Y, Takahashi S. Kokumai T, et al. Among authors: mukai t. J Clin Res Pediatr Endocrinol. 2024 Mar 11;16(1):102-105. doi: 10.4274/jcrpe.galenos.2022.2022-4-11. Epub 2022 Aug 19. J Clin Res Pediatr Endocrinol. 2024. PMID: 35983751 Free PMC article.

10

Partial paternal uniparental disomy of chromosome 6 in monozygotic twins with transient neonatal diabetes mellitus and macroglossia.

Suzuki S, Fujisawa D, Hashimoto K, Asano T, Maimaiti M, Matsuo K, Tanahashi Y, Mukai T, Fujieda K. Suzuki S, et al. Among authors: mukai t. Clin Genet. 2010 Dec;78(6):580-4. doi: 10.1111/j.1399-0004.2010.01433.x. Clin Genet. 2010. PMID: 20412110

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