Hai N - Search Results

1

Oliveira AM, Tazelaar HD, Wentzlaff KA, Kosugi NS, Hai N, Benson A, Miller DL, Yang P. Oliveira AM, et al. Among authors: hai n. Cancer. 2001 Jun 1;91(11):2104-9. doi: 10.1002/1097-0142(20010601)91:11<2104::aid-cncr1238>3.0.co;2-i. Cancer. 2001. PMID: 11391591

2

Two germline missense mutations at codons 804 and 806 of the RET proto-oncogene in the same allele in a patient with multiple endocrine neoplasia type 2B without codon 918 mutation.

Miyauchi A, Futami H, Hai N, Yokozawa T, Kuma K, Aoki N, Kosugi S, Sugano K, Yamaguchi K. Miyauchi A, et al. Among authors: hai n. Jpn J Cancer Res. 1999 Jan;90(1):1-5. doi: 10.1111/j.1349-7006.1999.tb00658.x. Jpn J Cancer Res. 1999. PMID: 10076558 Free PMC article.

3

A novel germline mutation of the MEN1 gene, L259del, in a patient with sporadic multiple endocrine neoplasia type 1 (MEN1).

Hai N, Muto G, Okamoto H, Tamada A, Abe R, Suzuki S, Kosugi S. Hai N, et al. Jpn J Clin Oncol. 2001 Mar;31(3):125-7. doi: 10.1093/jjco/hye021. Jpn J Clin Oncol. 2001. PMID: 11336326

4

A novel six-nucleotide insertion in exon 4 of the MEN1 gene, 878insCTGCAG, in three patients with familial insulinoma and primary hyperparathyroidism.

Okamoto H, Tamada A, Hai N, Doi M, Uchimura I, Hirata Y, Kosugi S. Okamoto H, et al. Among authors: hai n. Jpn J Clin Oncol. 2002 Sep;32(9):368-70. doi: 10.1093/jjco/hyf079. Jpn J Clin Oncol. 2002. PMID: 12417605

5

Germline MEN1 mutations in sixteen Japanese families with multiple endocrine neoplasia type 1 (MEN1).

Hai N, Aoki N, Matsuda A, Mori T, Kosugi S. Hai N, et al. Eur J Endocrinol. 1999 Nov;141(5):475-80. doi: 10.1530/eje.0.1410475. Eur J Endocrinol. 1999. PMID: 10576763

6

Gene diagnosis and clinical management of multiple endocrine neoplasia type 1 (MEN1).

Hai N, Kosugi S. Hai N, et al. Biomed Pharmacother. 2000 Jun;54 Suppl 1:47s-51s. doi: 10.1016/s0753-3322(00)80010-4. Biomed Pharmacother. 2000. PMID: 10914990 Review.

7

Clinical features of multiple endocrine neoplasia type 1 (MEN1) phenocopy without germline MEN1 gene mutations: analysis of 20 Japanese sporadic cases with MEN1.

Hai N, Aoki N, Shimatsu A, Mori T, Kosugi S. Hai N, et al. Clin Endocrinol (Oxf). 2000 Apr;52(4):509-18. doi: 10.1046/j.1365-2265.2000.00966.x. Clin Endocrinol (Oxf). 2000. PMID: 10762295

8

A novel activating mutation in the thyrotropin receptor gene in an autonomously functioning thyroid nodule developed by a Japanese patient.

Kosugi S, Hai N, Okamoto H, Sugawa H, Mori T. Kosugi S, et al. Among authors: hai n. Eur J Endocrinol. 2000 Oct;143(4):471-7. doi: 10.1530/eje.0.1430471. Eur J Endocrinol. 2000. PMID: 11022192

9

Recent trends in the management of Graves' hyperthyroidism in Japan: opinion survey results, especially on the combination therapy of antithyroid drug and thyroid hormone.

Mori T, Sugawa H, Kosugi S, Ueda M, Hai N, Matsuda A. Mori T, et al. Among authors: hai n. Endocr J. 1997 Aug;44(4):509-17. doi: 10.1507/endocrj.44.509. Endocr J. 1997. PMID: 9447283 Free article.

10

Aspartate-474 in the first exoplasmic loop of the thyrotropin receptor is crucial for receptor activation.

Kosugi S, Matsuda A, Hai N, Aoki N, Sugawa H, Mori T. Kosugi S, et al. Among authors: hai n. FEBS Lett. 1997 Apr 7;406(1-2):139-41. doi: 10.1016/s0014-5793(97)00256-1. FEBS Lett. 1997. PMID: 9109404 Free article.

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