Utsunomiya M - Search Results

1

Absence of linkage of familial intracranial aneurysms to 7q11 in highly aggregated Japanese families.

Yamada S, Utsunomiya M, Inoue K, Nozaki K, Miyamoto S, Hashimoto N, Takenaka K, Yoshinaga T, Koizumi A. Yamada S, et al. Among authors: utsunomiya m. Stroke. 2003 Apr;34(4):892-900. doi: 10.1161/01.STR.0000062887.71400.B4. Epub 2003 Mar 20. Stroke. 2003. PMID: 12649519

2

Genome-wide scan for Japanese familial intracranial aneurysms: linkage to several chromosomal regions.

Yamada S, Utsunomiya M, Inoue K, Nozaki K, Inoue S, Takenaka K, Hashimoto N, Koizumi A. Yamada S, et al. Among authors: utsunomiya m. Circulation. 2004 Dec 14;110(24):3727-33. doi: 10.1161/01.CIR.0000143077.23367.18. Epub 2004 Nov 29. Circulation. 2004. PMID: 15569837

3

[An overview of genetic analysis for neurosurgical diseases and disorders].

Koizumi A, Yamada S, Utsunomiya M, Inoue K, Yorifuji J, Nozaki K, Hashimoto N, Takenaka K, Iwama T, Suzuki M, Nomura S, Yamakawa H, Abe M, Tabuchi K, Matsuda M. Koizumi A, et al. Among authors: utsunomiya m. No Shinkei Geka. 2004 Dec;32(12):1203-13. No Shinkei Geka. 2004. PMID: 15605690 Review. Japanese. No abstract available.

4

Mutation analysis in PKD1 of Japanese autosomal dominant polycystic kidney disease patients.

Inoue S, Inoue K, Utsunomiya M, Nozaki J, Yamada Y, Iwasa T, Mori E, Yoshinaga T, Koizumi A. Inoue S, et al. Among authors: utsunomiya m. Hum Mutat. 2002 Jun;19(6):622-8. doi: 10.1002/humu.10080. Hum Mutat. 2002. PMID: 12007219

5

A new locus for a dominant form of multinodular goiter on 3q26.1-q26.3.

Takahashi T, Nozaki J, Komatsu M, Wada Y, Utsunomiya M, Inoue K, Takada G, Koizumi A. Takahashi T, et al. Among authors: utsunomiya m. Biochem Biophys Res Commun. 2001 Jun 15;284(3):650-4. doi: 10.1006/bbrc.2001.4998. Biochem Biophys Res Commun. 2001. PMID: 11396950

6

Evaluation of a mass screening program for lysinuric protein intolerance in the northern part of Japan.

Koizumi A, Matsuura N, Inoue S, Utsunomiya M, Nozaki J, Inoue K, Takasago Y; Mass Screening Group. Koizumi A, et al. Among authors: utsunomiya m. Genet Test. 2003 Spring;7(1):29-35. doi: 10.1089/109065703321560903. Genet Test. 2003. PMID: 12820699

7

Long-acting gonadotropin-releasing hormone analogue treatment for central precocious puberty in maternal uniparental disomy chromosome 14.

Takahashi I, Takahashi T, Utsunomiya M, Takada G, Koizumi A. Takahashi I, et al. Among authors: utsunomiya m. Tohoku J Exp Med. 2005 Dec;207(4):333-8. doi: 10.1620/tjem.207.333. Tohoku J Exp Med. 2005. PMID: 16272804 Free article.

8

A PTPN11 gene mutation (Y63C) causing Noonan syndrome is not associated with short stature in general population.

Takahashi I, Utsunomiya M, Inoue K, Takahashi T, Nozaki J, Wada Y, Takada G, Koizumi A. Takahashi I, et al. Among authors: utsunomiya m. Tohoku J Exp Med. 2006 Mar;208(3):255-9. doi: 10.1620/tjem.208.255. Tohoku J Exp Med. 2006. PMID: 16498234 Free article.

9

A case of delayed necrosis of reconstructed colon after esophagectomy.

Yokota K, Kitagawa H, Namikawa T, Utsunomiya M, Seo S. Yokota K, et al. Among authors: utsunomiya m. Clin J Gastroenterol. 2024 Oct;17(5):799-802. doi: 10.1007/s12328-024-02009-7. Epub 2024 Jun 25. Clin J Gastroenterol. 2024. PMID: 38918307

10

Benefit of a laparoscopic jejunostomy feeding catheter insertion to prevent bowel obstruction associated with feeding jejunostomy after esophagectomy.

Kitagawa H, Yokota K, Utsunomiya M, Tanaka T, Namikawa T, Kobayashi M, Seo S. Kitagawa H, et al. Among authors: utsunomiya m. Sci Rep. 2024 Feb 21;14(1):4298. doi: 10.1038/s41598-024-55020-w. Sci Rep. 2024. PMID: 38383707 Free PMC article.

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