Kikuta K - Search Results

1

[-215G>A; IVS3+2T>C] mutation in the SPINK1 gene causes exon 3 skipping and loss of the trypsin binding site.

Kume K, Masamune A, Kikuta K, Shimosegawa T. Kume K, et al. Among authors: kikuta k. Gut. 2006 Aug;55(8):1214. doi: 10.1136/gut.2006.095752. Gut. 2006. PMID: 16849362 Free PMC article. No abstract available.

2

A loss-of-function p.G191R variant in the anionic trypsinogen (PRSS2) gene in Japanese patients with pancreatic disorders.

Kume K, Masamune A, Takagi Y, Kikuta K, Watanabe T, Satoh K, Satoh A, Hirota M, Hamada S, Shimosegawa T. Kume K, et al. Among authors: kikuta k. Gut. 2009 Jun;58(6):820-4. doi: 10.1136/gut.2008.151688. Epub 2008 Dec 3. Gut. 2009. PMID: 19052022

3

Fibrinogen induces cytokine and collagen production in pancreatic stellate cells.

Masamune A, Kikuta K, Watanabe T, Satoh K, Hirota M, Hamada S, Shimosegawa T. Masamune A, et al. Among authors: kikuta k. Gut. 2009 Apr;58(4):550-9. doi: 10.1136/gut.2008.154401. Epub 2008 Dec 3. Gut. 2009. PMID: 19052021

4

Introduction to tractography-guided navigation: using 3-tesla magnetic resonance tractography in surgery for cerebral arteriovenous malformations.

Kikuta K, Takagi Y, Nozaki K, Hashimoto N. Kikuta K, et al. Acta Neurochir Suppl. 2008;103:11-4. doi: 10.1007/978-3-211-76589-0_4. Acta Neurochir Suppl. 2008. PMID: 18496939 Clinical Trial.

5

The presence of multiple microbleeds as a predictor of subsequent cerebral hemorrhage in patients with moyamoya disease.

Kikuta K, Takagi Y, Nozaki K, Sawamoto N, Fukuyama H, Hashimoto N. Kikuta K, et al. Neurosurgery. 2008 Jan;62(1):104-11, discussion 111-2. doi: 10.1227/01.NEU.0000311067.41239.E6. Neurosurgery. 2008. PMID: 18300897

6

Histological features of middle cerebral arteries from patients treated for Moyamoya disease.

Takagi Y, Kikuta K, Nozaki K, Hashimoto N. Takagi Y, et al. Among authors: kikuta k. Neurol Med Chir (Tokyo). 2007 Jan;47(1):1-4. doi: 10.2176/nmc.47.1. Neurol Med Chir (Tokyo). 2007. PMID: 17245006 Free article.

7

Autosomal dominant moyamoya disease maps to chromosome 17q25.3.

Mineharu Y, Liu W, Inoue K, Matsuura N, Inoue S, Takenaka K, Ikeda H, Houkin K, Takagi Y, Kikuta K, Nozaki K, Hashimoto N, Koizumi A. Mineharu Y, et al. Among authors: kikuta k. Neurology. 2008 Jun 10;70(24 Pt 2):2357-63. doi: 10.1212/01.wnl.0000291012.49986.f9. Epub 2008 May 7. Neurology. 2008. PMID: 18463369

8

Absence epilepsy associated with moyamoya disease. Case report.

Kikuta K, Takagi Y, Arakawa Y, Miyamoto S, Hashimoto N. Kikuta K, et al. J Neurosurg. 2006 Apr;104(4 Suppl):265-8. doi: 10.3171/ped.2006.104.4.265. J Neurosurg. 2006. PMID: 16619638

9

Risk factors for subsequent hemorrhage in patients with cerebral arteriovenous malformations.

Yamada S, Takagi Y, Nozaki K, Kikuta K, Hashimoto N. Yamada S, et al. Among authors: kikuta k. J Neurosurg. 2007 Nov;107(5):965-72. doi: 10.3171/JNS-07/11/0965. J Neurosurg. 2007. PMID: 17977268

10

Histological analysis of microbleed after surgical resection in a patient with moyamoya disease.

Kikuta K, Takagi Y, Nozaki K, Okada T, Hashimoto N. Kikuta K, et al. Neurol Med Chir (Tokyo). 2007 Dec;47(12):564-7. doi: 10.2176/nmc.47.564. Neurol Med Chir (Tokyo). 2007. PMID: 18159142 Free article.

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