Jo W - Search Results

1

Case study of a 15-year-old boy with McCune-Albright syndrome combined with pituitary gigantism: effect of octreotide-long acting release (LAR) and cabergoline therapy.

Tajima T, Tsubaki J, Ishizu K, Jo W, Ishi N, Fujieda K. Tajima T, et al. Among authors: jo w. Endocr J. 2008 Jul;55(3):595-9. doi: 10.1507/endocrj.k07e-042. Epub 2008 Apr 30. Endocr J. 2008. PMID: 18445999 Free article.

2

Congenital Hypothyroidism Caused by a PAX8 Gene Mutation Manifested as Sodium/Iodide Symporter Gene Defect.

Jo W, Ishizu K, Fujieda K, Tajima T. Jo W, et al. J Thyroid Res. 2010;2010:619013. doi: 10.4061/2010/619013. Epub 2009 Dec 9. J Thyroid Res. 2010. PMID: 21048839 Free PMC article.

3

Molecular analysis of the GATA3 gene in five Japanese patients with HDR syndrome.

Nakamura A, Fujiwara F, Hasegawa Y, Ishizu K, Mabe A, Nakagawa H, Nagasaki K, Jo W, Tajima T. Nakamura A, et al. Among authors: jo w. Endocr J. 2011;58(2):123-30. doi: 10.1507/endocrj.k10e-246. Epub 2010 Dec 10. Endocr J. 2011. PMID: 21157112 Free article.

4

Development of endometrial carcinoma in a patient with leprechaunism (donohue syndrome).

Jo W, Sudo S, Nakamura A, Endo D, Konno Y, Ishizu K, Tajima T. Jo W, et al. Clin Pediatr Endocrinol. 2013 Apr;22(2):33-8. doi: 10.1292/cpe.22.33. Epub 2013 Apr 26. Clin Pediatr Endocrinol. 2013. PMID: 23990696 Free PMC article.

5

Elevated free thyroxine levels detected by a neonatal screening system.

Tajima T, Jo W, Fujikura K, Fukushi M, Fujieda K. Tajima T, et al. Among authors: jo w. Pediatr Res. 2009 Sep;66(3):312-6. doi: 10.1203/PDR.0b013e3181b1bcbd. Pediatr Res. 2009. PMID: 19542904

6

A Novel Mutation of the Glucokinase Gene in Maturity-onset Diabetes of the Young Type 2 (MODY2).

Jo W, Fujieda K, Tajima T. Jo W, et al. Clin Pediatr Endocrinol. 2010 Apr;19(2):45-6. doi: 10.1297/cpe.19.45. Epub 2010 May 22. Clin Pediatr Endocrinol. 2010. PMID: 23926378 Free PMC article. No abstract available.

7

A Novel Splicing Mutation of the GNAS Gene in a Patient with Pseudohypoparathyroidism Ia.

Nakamura A, Hostubo T, Jo W, Ishizu K, Tajima T. Nakamura A, et al. Among authors: jo w. Clin Pediatr Endocrinol. 2011 Jan;20(1):21-3. doi: 10.1297/cpe.20.21. Epub 2011 Mar 26. Clin Pediatr Endocrinol. 2011. PMID: 23926390 Free PMC article. No abstract available.

8

A novel PAX4 mutation in a Japanese patient with maturity-onset diabetes of the young.

Jo W, Endo M, Ishizu K, Nakamura A, Tajima T. Jo W, et al. Tohoku J Exp Med. 2011 Feb;223(2):113-8. doi: 10.1620/tjem.223.113. Tohoku J Exp Med. 2011. PMID: 21263211 Free article.

9

A Case of Novel Mutation of HNF1B in Maturity-onset Diabetes of the Young Type 5 (MODY5).

Jo W, Sano H, Sudo A, Matsunami Y, Kawamura N, Tajima T. Jo W, et al. Clin Pediatr Endocrinol. 2012 Jul;21(3):53-5. doi: 10.1297/cpe.21.53. Epub 2012 Jul 25. Clin Pediatr Endocrinol. 2012. PMID: 23926411 Free PMC article. No abstract available.

10

Three-dimensional customized artificial grafts functionalized with biomimetic softness and anticoagulant heparin-dopamine surface modification: Preclinical study for practical applications.

Kim CH, Kim Y, Karna S, Yoo SM, Lee JH, Kim YJ, Lee JH, Jo WM, Park SH, Kim TH. Kim CH, et al. Among authors: jo wm. Int J Biol Macromol. 2025 Jan 17;299:140002. doi: 10.1016/j.ijbiomac.2025.140002. Online ahead of print. Int J Biol Macromol. 2025. PMID: 39828176 Free article.

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