Hotsubo T - Search Results

1

Treatment of Hypothyroidism due to Iodine Deficiency Using Daily Powdered Kelp in Patients Receiving Long-term Total Enteral Nutrition.

Takeuchi T, Kamasaki H, Hotsubo T, Tsutsumi H. Takeuchi T, et al. Among authors: hotsubo t. Clin Pediatr Endocrinol. 2011 Jul;20(3):51-5. doi: 10.1297/cpe.20.51. Epub 2011 Oct 7. Clin Pediatr Endocrinol. 2011. PMID: 23926395 Free PMC article.

2

N-terminal pro-brain natriuretic Peptide as a useful diagnostic marker of acute Kawasaki disease in children.

Shiraishi M, Fuse S, Mori T, Doyama A, Honjyo S, Hoshino Y, Hoshino E, Kawaguchi A, Kuroiwa Y, Hotsubo T. Shiraishi M, et al. Among authors: hotsubo t. Circ J. 2013;77(8):2097-101. doi: 10.1253/circj.cj-12-1281. Epub 2013 Apr 24. Circ J. 2013. PMID: 23615024 Free article.

3

Rotavirus encephalitis and cerebellitis with reversible magnetic resonance signal changes.

Mori T, Morii M, Kuroiwa Y, Hotsubo T, Fuse S, Tsustumi H. Mori T, et al. Among authors: hotsubo t. Pediatr Int. 2011 Apr;53(2):252-5. doi: 10.1111/j.1442-200X.2010.03221.x. Pediatr Int. 2011. PMID: 21501312 No abstract available.

4

Investigation of iodine deficient state and iodine supplementation in patients with severe motor and intellectual disabilities on long-term total enteral nutrition.

Takeuchi T, Kamasaki H, Yoto Y, Honjo T, Tsugawa S, Hotsubo T, Tsutsumi H. Takeuchi T, et al. Among authors: hotsubo t. Endocr J. 2012;59(8):697-703. doi: 10.1507/endocrj.ej11-0361. Epub 2012 May 25. Endocr J. 2012. PMID: 22673532 Free article.

5

Results from 28 years of newborn screening for congenital adrenal hyperplasia in sapporo.

Morikawa S, Nakamura A, Fujikura K, Fukushi M, Hotsubo T, Miyata J, Ishizu K, Tajima T. Morikawa S, et al. Among authors: hotsubo t. Clin Pediatr Endocrinol. 2014 Apr;23(2):35-43. doi: 10.1297/cpe.23.35. Epub 2014 Apr 20. Clin Pediatr Endocrinol. 2014. PMID: 24790385 Free PMC article.

6

Familial short stature is associated with a novel dominant-negative heterozygous insulin-like growth factor 1 receptor (IGF1R) mutation.

Kawashima Y, Hakuno F, Okada S, Hotsubo T, Kinoshita T, Fujimoto M, Nishimura R, Fukushima T, Hanaki K, Takahashi S, Kanzaki S. Kawashima Y, et al. Among authors: hotsubo t. Clin Endocrinol (Oxf). 2014 Aug;81(2):312-4. doi: 10.1111/cen.12317. Epub 2013 Sep 30. Clin Endocrinol (Oxf). 2014. PMID: 24033502 No abstract available.

7

Neonatal screening for congenital adrenal hyperplasia in Japan.

Tajima T, Fujikura K, Fukushi M, Hotsubo T, Mitsuhashi Y. Tajima T, et al. Among authors: hotsubo t. Pediatr Endocrinol Rev. 2012 Oct;10 Suppl 1:72-8. Pediatr Endocrinol Rev. 2012. PMID: 23330248 Review.

8

Three novel IGSF1 mutations in four Japanese patients with X-linked congenital central hypothyroidism.

Nakamura A, Bak B, Silander TL, Lam J, Hotsubo T, Yorifuji T, Ishizu K, Bernard DJ, Tajima T. Nakamura A, et al. Among authors: hotsubo t. J Clin Endocrinol Metab. 2013 Oct;98(10):E1682-91. doi: 10.1210/jc.2013-1224. Epub 2013 Aug 21. J Clin Endocrinol Metab. 2013. PMID: 23966245 Free article.

9

The prevalence of mitochondrial gene mutations in childhood diabetes in Japan.

Matsuura N, Suzuki S, Yokota Y, Kazahari K, Kazahari M, Toyota T, Hirai M, Okuno A, Harada S, Fukushima N, Koike A, Ito Y, Hotsubo T. Matsuura N, et al. Among authors: hotsubo t. J Pediatr Endocrinol Metab. 1999 Jan-Feb;12(1):27-30. doi: 10.1515/jpem.1999.12.1.27. J Pediatr Endocrinol Metab. 1999. PMID: 10392345

10

Comparison of an immunochromatography test with multiplex reverse transcription-PCR for rapid diagnosis of respiratory syncytial virus infections.

Kuroiwa Y, Nagai K, Okita L, Ukae S, Mori T, Hotsubo T, Tsutsumi H. Kuroiwa Y, et al. Among authors: hotsubo t. J Clin Microbiol. 2004 Oct;42(10):4812-4. doi: 10.1128/JCM.42.10.4812-4814.2004. J Clin Microbiol. 2004. PMID: 15472348 Free PMC article.

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