Hattori N - Search Results

1

Recurrent embolic strokes associated with vertical atlantoaxial subluxation in a patient with rheumatoid arthritis: a case report and review of literature.

Kuroki T, Ueno Y, Takeda I, Kambe T, Nishioka K, Shimura H, Itoh M, Hattori N, Urabe T. Kuroki T, et al. Among authors: hattori n. J Stroke Cerebrovasc Dis. 2013 Nov;22(8):e676-81. doi: 10.1016/j.jstrokecerebrovasdis.2013.07.010. Epub 2013 Aug 2. J Stroke Cerebrovasc Dis. 2013. PMID: 23911241 Review.

2

Expression of glucose transporters in rat brain following transient focal ischemic injury.

Urabe T, Hattori N, Nagamatsu S, Sawa H, Mizuno Y. Urabe T, et al. Among authors: hattori n. J Neurochem. 1996 Jul;67(1):265-71. doi: 10.1046/j.1471-4159.1996.67010265.x. J Neurochem. 1996. PMID: 8667001

3

Postischemic accumulation of lipid peroxidation products in the rat brain: immunohistochemical detection of 4-hydroxy-2-nonenal modified proteins.

Yoshino H, Hattori N, Urabe T, Uchida K, Tanaka M, Mizuno Y. Yoshino H, et al. Among authors: hattori n. Brain Res. 1997 Aug 29;767(1):81-6. doi: 10.1016/s0006-8993(97)00616-1. Brain Res. 1997. PMID: 9365018

4

Colocalization of Bcl-2 and 4-hydroxynonenal modified proteins in microglial cells and neurons of rat brain following transient focal ischemia.

Urabe T, Hattori N, Yoshikawa M, Yoshino H, Uchida K, Mizuno Y. Urabe T, et al. Among authors: hattori n. Neurosci Lett. 1998 May 15;247(2-3):159-62. doi: 10.1016/s0304-3940(98)00311-5. Neurosci Lett. 1998. PMID: 9655617

5

Immunohistochemical and subcellular localization of Parkin protein: absence of protein in autosomal recessive juvenile parkinsonism patients.

Shimura H, Hattori N, Kubo S, Yoshikawa M, Kitada T, Matsumine H, Asakawa S, Minoshima S, Yamamura Y, Shimizu N, Mizuno Y. Shimura H, et al. Among authors: hattori n. Ann Neurol. 1999 May;45(5):668-72. doi: 10.1002/1531-8249(199905)45:5<668::aid-ana19>3.0.co;2-z. Ann Neurol. 1999. PMID: 10319893

6

Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase.

Shimura H, Hattori N, Kubo Si, Mizuno Y, Asakawa S, Minoshima S, Shimizu N, Iwai K, Chiba T, Tanaka K, Suzuki T. Shimura H, et al. Among authors: hattori n. Nat Genet. 2000 Jul;25(3):302-5. doi: 10.1038/77060. Nat Genet. 2000. PMID: 10888878

7

Progress in the clinical and molecular genetics of familial parkinsonism.

Kitada T, Asakawa S, Matsumine H, Hattori N, Shimura H, Minoshima S, Shimizu N, Mizuno Y. Kitada T, et al. Among authors: hattori n. Neurogenetics. 2000 Mar;2(4):207-18. doi: 10.1007/s100489900083. Neurogenetics. 2000. PMID: 10983716 Review.

8

Accumulation of 4-hydroxynonenal-modified proteins in hippocampal CA1 pyramidal neurons precedes delayed neuronal damage in the gerbil brain.

Urabe T, Yamasaki Y, Hattori N, Yoshikawa M, Uchida K, Mizuno Y. Urabe T, et al. Among authors: hattori n. Neuroscience. 2000;100(2):241-50. doi: 10.1016/s0306-4522(00)00264-5. Neuroscience. 2000. PMID: 11008164

9

Autosomal recessive juvenile parkinsonism: a key to understanding nigral degeneration in sporadic Parkinson's disease.

Hattori N, Shimura H, Kubo S, Kitada T, Wang M, Asakawa S, Minashima S, Shimizu N, Suzuki T, Tanaka K, Mizuno Y. Hattori N, et al. Neuropathology. 2000 Sep;20 Suppl:S85-90. doi: 10.1046/j.1440-1789.2000.00312.x. Neuropathology. 2000. PMID: 11037196 Review.

10

Importance of familial Parkinson's disease and parkinsonism to the understanding of nigral degeneration in sporadic Parkinson's disease.

Hattori N, Shimura H, Kubo S, Wang M, Shimizu N, Tanaka K, Mizuno Y. Hattori N, et al. J Neural Transm Suppl. 2000;(60):101-16. doi: 10.1007/978-3-7091-6301-6_6. J Neural Transm Suppl. 2000. PMID: 11205133 Review.

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