Kobayashi H - Search Results

1

Kobayashi H, Hino M, Inoue T, Nii E, Ikeda K, Son C, Iwakura T, Ishihara T, Ogawa Y. Kobayashi H, et al. Am J Med Genet A. 2005 Apr 30;134(3):341-3. doi: 10.1002/ajmg.a.30596. Am J Med Genet A. 2005. PMID: 15690404 No abstract available.

2

Missense mutation of TRPS1 in a family of tricho-rhino-phalangeal syndrome type III.

Kobayashi H, Hino M, Shimodahira M, Iwakura T, Ishihara T, Ikekubo K, Ogawa Y, Nakao K, Kurahachi H. Kobayashi H, et al. Am J Med Genet. 2002 Jan 1;107(1):26-9. doi: 10.1002/ajmg.10081. Am J Med Genet. 2002. PMID: 11807863

3

A Novel homozygous missense mutation of melanocortin-4 receptor (MC4R) in a Japanese woman with severe obesity.

Kobayashi H, Ogawa Y, Shintani M, Ebihara K, Shimodahira M, Iwakura T, Hino M, Ishihara T, Ikekubo K, Kurahachi H, Nakao K. Kobayashi H, et al. Diabetes. 2002 Jan;51(1):243-6. doi: 10.2337/diabetes.51.1.243. Diabetes. 2002. PMID: 11756348

4

Evaluation of a 1 step TRAb assay for the detection of high-affinity components to hTSHR: evidences indicating superiority of the assay in the lower TRAb range.

Ishihara T, Saiki Y, Ikekubo K, Hino M, Ikeda K, Son C, Iwakura T, Kobayashi H, Mori T. Ishihara T, et al. Among authors: kobayashi h. Endocr J. 2006 Feb;53(1):147-55. doi: 10.1507/endocrj.53.147. Endocr J. 2006. PMID: 16543685 Free article.

5

Immeasurably low and non-TRH-stimulatable TSH associated with normal I-123 uptake in two goitrous euthyroid patients: possible existence of other thyroid-hormone regulated thyroid stimulators other than TSH.

Ikekubo K, Hino M, Saiki Y, Son C, Iwakura T, Kobayashi H, Ishihara T. Ikekubo K, et al. Among authors: kobayashi h. Endocr J. 2005 Feb;52(1):61-8. doi: 10.1507/endocrj.52.61. Endocr J. 2005. PMID: 15758559 Free article.

6

A novel heterozygous deletion frameshift mutation of GATA3 in a Japanese kindred with the hypoparathyroidism, deafness and renal dysplasia syndrome.

Kobayashi H, Kasahara M, Hino M, Yoshimura H, Takahara S, Ikeda K, Son C, Iwakura T, Yoshimoto A, Ishihara T, Ogawa Y. Kobayashi H, et al. J Endocrinol Invest. 2006 Oct;29(9):851-3. doi: 10.1007/BF03347383. J Endocrinol Invest. 2006. PMID: 17114920 No abstract available.

7

A novel heterozygous splice-site mutation of LEM domain-containing 3 in a Japanese kindred with Buschke-Ollendorff syndrome.

Kobayashi H, Kasahara M, Hino M, Takahara S, Ikeda K, Son C, Iwakura T, Matsuoka N, Yoshimoto A, Ohgo N, Kasai R, Ishihara T, Ogawa Y. Kobayashi H, et al. J Endocrinol Invest. 2007 Mar;30(3):263-5. doi: 10.1007/BF03347437. J Endocrinol Invest. 2007. PMID: 17505164 No abstract available.

8

[No title available]

Kobayashi H, Shimodahira M, Iwakura T, Ishihara T, Kurahachi H, Hino M, Ikekubo K, Ogawa Y, Nakao K. Kobayashi H, et al. Clin Calcium. 2002 Jan;12(1):124-7. Clin Calcium. 2002. PMID: 15775290 Japanese. No abstract available.

9

Successful treatment of locally advanced anaplastic thyroid carcinoma by chemotherapy and hyperfractionated radiotherapy.

Shinohara S, Kikuchi M, Naito Y, Fujiwara K, Hori S, Tona Y, Yamazaki H, Kobayashi H, Ishihara T. Shinohara S, et al. Among authors: kobayashi h. Auris Nasus Larynx. 2009 Dec;36(6):729-32. doi: 10.1016/j.anl.2009.02.001. Epub 2009 Mar 9. Auris Nasus Larynx. 2009. PMID: 19269756

10

[Melanocortin-4 receptor gene mutations associated with obesity].

Kobayashi H. Kobayashi H. Nihon Rinsho. 2006 Sep 28;Suppl 3:260-3. Nihon Rinsho. 2006. PMID: 17022542 Review. Japanese. No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

9,527 results

Search Page

Filters