Kitajima I - Search Results

1

[Cerebral venous sinus thrombosis in the patient with multiple sclerosis associated with congenital antithrombin deficiency].

Kanaya Y, Takamatsu K, Shimoe Y, Niimi H, Kitajima I, Kuriyama M. Kanaya Y, et al. Among authors: kitajima i. Rinsho Shinkeigaku. 2016 Apr 28;56(4):248-54. doi: 10.5692/clinicalneurol.cn-000796. Epub 2016 Mar 24. Rinsho Shinkeigaku. 2016. PMID: 27010094 Review. Japanese.

2

[Establishment of the rapid, hypersensitive testing systems for sepsis/SIRS].

Kitajima I, Niimi H. Kitajima I, et al. Rinsho Byori. 2012 Jan;60(1):46-51. Rinsho Byori. 2012. PMID: 22416456 Review. Japanese.

3

[Genetic diagnostics of pathogenic splicing abnormalities in the clinical laboratory--pitfalls and screening approaches].

Niimi H, Ogawa T, Note R, Hayashi S, Ueno T, Harada K, Uji Y, Kitajima I. Niimi H, et al. Among authors: kitajima i. Rinsho Byori. 2010 Dec;58(12):1162-8. Rinsho Byori. 2010. PMID: 21348235 Japanese.

4

Diagnosis of cerebral cortical vein thrombosis with T2* weighted magnetic resonance imaging.

Katayama Y, Kitajima I, Niimi H, Kitahara H, Kawai H. Katayama Y, et al. Among authors: kitajima i. BMJ Case Rep. 2009;2009:bcr03.2009.1651. doi: 10.1136/bcr.03.2009.1651. Epub 2009 Sep 6. BMJ Case Rep. 2009. PMID: 21894245 Free PMC article.

5

Factor X heterozygous mutation in a patient with potential risk of bleeding: A case report.

Arita K, Niimi H, Yamagishi N, Ueno T, Kitajima I, Sugiyama T. Arita K, et al. Among authors: kitajima i. Medicine (Baltimore). 2018 Jun;97(23):e10950. doi: 10.1097/MD.0000000000010950. Medicine (Baltimore). 2018. PMID: 29879041 Free PMC article.

6

[Trend survey of ocular infections with bacteria at Toyama University Hospital over the past six years--from the standpoint of laboratory examination].

Kubota T, Hayashi S, Niimi H, Kitajima I. Kubota T, et al. Among authors: kitajima i. Rinsho Byori. 2012 Jul;60(7):605-11. Rinsho Byori. 2012. PMID: 22973718 Japanese.

7

Increased cerebrospinal fluid adenosine 5'-triphosphate in patients with amyotrophic lateral sclerosis.

Nukui T, Matsui A, Niimi H, Sugimoto T, Hayashi T, Dougu N, Konishi H, Yamamoto M, Anada R, Matsuda N, Kitajima I, Nakatsuji Y. Nukui T, et al. Among authors: kitajima i. BMC Neurol. 2021 Jun 30;21(1):255. doi: 10.1186/s12883-021-02288-4. BMC Neurol. 2021. PMID: 34193068 Free PMC article.

8

Cerebrospinal fluid ATP as a potential biomarker in patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke like episodes (MELAS).

Nukui T, Matsui A, Niimi H, Yamamoto M, Matsuda N, Piao JL, Noguchi K, Kitajima I, Nakatsuji Y. Nukui T, et al. Among authors: kitajima i. Mitochondrion. 2020 Jan;50:145-148. doi: 10.1016/j.mito.2019.11.001. Epub 2019 Nov 19. Mitochondrion. 2020. PMID: 31756516

9

[Effect of ISO15189 accreditation in Clinical Laboratory Center of Toyama University Hospital].

Uji Y, Kawashima T, Kuwabara T, Yoshida C, Niimi H, Kitajima I. Uji Y, et al. Among authors: kitajima i. Rinsho Byori. 2009 Aug;57(8):752-60. Rinsho Byori. 2009. PMID: 19764410 Japanese.

10

A novel Y231del mutation of HFE in hereditary haemochromatosis provides in vivo evidence that the Huh-7 is a human haemochromatotic cell line.

Takano A, Niimi H, Atarashi Y, Sawasaki T, Terasaki T, Nakabayashi T, Kitajima I, Tobe K, Takahara T. Takano A, et al. Among authors: kitajima i. Liver Int. 2011 Nov;31(10):1593-7. doi: 10.1111/j.1478-3231.2011.02620.x. Epub 2011 Aug 17. Liver Int. 2011. PMID: 22093335

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