Nakamura Y - Search Results

1

Mutations of human butyrylcholinesterase gene in a family with hypocholinesterasemia.

Iida S, Kinoshita M, Fujii H, Moriyama Y, Nakamura Y, Yura N, Moriwaki K. Iida S, et al. Among authors: nakamura y. Hum Mutat. 1995;6(4):349-51. doi: 10.1002/humu.1380060411. Hum Mutat. 1995. PMID: 8680411 No abstract available.

2

A heterozygous germline mutation of the PTEN/MMAC1 gene in a patient with Cowden disease.

Iida S, Nakamura Y, Fujii H, Kimura M, Moriwaki K. Iida S, et al. Among authors: nakamura y. Int J Mol Med. 1998 Mar;1(3):565-8. doi: 10.3892/ijmm.1.3.565. Int J Mol Med. 1998. PMID: 9852263

3

Quantitative comparison of aromatase induction by dexamethasone in fibroblasts from a patient with familial cortisol resistance and a patient with cortisol hyperreactive syndrome.

Iida S, Moriwaki K, Fujii H, Gomi M, Tsugawa M, Nakamura Y, Kitani T, Tarui S. Iida S, et al. Among authors: nakamura y. J Clin Endocrinol Metab. 1991 Jul;73(1):192-6. doi: 10.1210/jcem-73-1-192. J Clin Endocrinol Metab. 1991. PMID: 2045469

4

A patient with hypocortisolism and Cushing's syndrome-like manifestations: cortisol hyperreactive syndrome.

Iida S, Nakamura Y, Fujii H, Nishimura J, Tsugawa M, Gomi M, Fukata J, Tarui S, Moriwaki K, Kitani T. Iida S, et al. Among authors: nakamura y. J Clin Endocrinol Metab. 1990 Mar;70(3):729-37. doi: 10.1210/jcem-70-3-729. J Clin Endocrinol Metab. 1990. PMID: 2155254

5

Human SA gene locus as a candidate locus for essential hypertension.

Iwai N, Ohmichi N, Hanai K, Nakamura Y, Kinoshita M. Iwai N, et al. Among authors: nakamura y. Hypertension. 1994 Mar;23(3):375-80. doi: 10.1161/01.hyp.23.3.375. Hypertension. 1994. PMID: 7907320

6

DD genotype of the angiotensin-converting enzyme gene is a risk factor for left ventricular hypertrophy.

Iwai N, Ohmichi N, Nakamura Y, Kinoshita M. Iwai N, et al. Among authors: nakamura y. Circulation. 1994 Dec;90(6):2622-8. doi: 10.1161/01.cir.90.6.2622. Circulation. 1994. PMID: 7994801

7

The genotype of the angiotensin-converting enzyme gene and global left ventricular dysfunction after myocardial infarction.

Ohmichi N, Iwai N, Nakamura Y, Kinoshita M. Ohmichi N, et al. Among authors: nakamura y. Am J Cardiol. 1995 Aug 15;76(5):326-9. doi: 10.1016/s0002-9149(99)80094-0. Am J Cardiol. 1995. PMID: 7639154

8

Predictors of ischemic stroke in non-rheumatic atrial fibrillation.

Yoshida M, Nakamura Y, Higashikawa M, Kinoshita M. Yoshida M, et al. Among authors: nakamura y. Int J Cardiol. 1996 Sep;56(1):61-70. doi: 10.1016/0167-5273(96)02726-x. Int J Cardiol. 1996. PMID: 8891806

9

Evaluation of cardiac sympathetic innervation with iodine-123-metaiodobenzylguanidine imaging in silent myocardial ischemia.

Matsuo S, Takahashi M, Nakamura Y, Kinoshita M. Matsuo S, et al. Among authors: nakamura y. J Nucl Med. 1996 May;37(5):712-7. J Nucl Med. 1996. PMID: 8965132 Free article.

10

Somatic mutations of a human mismatch repair gene, hMLH1, in tumors from patients with multiple primary cancers.

Sasaki S, Horii A, Shimada M, Han HJ, Yanagisawa A, Muto T, Nakamura Y. Sasaki S, et al. Among authors: nakamura y. Hum Mutat. 1996;7(3):275-8. doi: 10.1002/(SICI)1098-1004(1996)7:3<275::AID-HUMU15>3.0.CO;2-#. Hum Mutat. 1996. PMID: 8829664 No abstract available.

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