Hattori N - Search Results

1

Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study.

Gouider-Khouja N, Larnaout A, Amouri R, Sfar S, Belal S, Ben Hamida C, Ben Hamida M, Hattori N, Mizuno Y, Hentati F. Gouider-Khouja N, et al. Among authors: hattori n. Parkinsonism Relat Disord. 2003 Jun;9(5):247-51. doi: 10.1016/s1353-8020(03)00016-6. Parkinsonism Relat Disord. 2003. PMID: 12781588

2

Sensory neuropathy in autosomal recessive juvenile parkinsonism (PARK2).

Okuma Y, Hattori N, Mizuno Y. Okuma Y, et al. Among authors: hattori n. Parkinsonism Relat Disord. 2003 Jun;9(5):313-4. doi: 10.1016/s1353-8020(02)00114-1. Parkinsonism Relat Disord. 2003. PMID: 12781600

3

Pseudo-autosomal dominant inheritance of PARK2: two families with parkin gene mutations.

Kobayashi T, Matsumine H, Zhang J, Imamichi Y, Mizuno Y, Hattori N. Kobayashi T, et al. Among authors: hattori n. J Neurol Sci. 2003 Mar 15;207(1-2):11-7. doi: 10.1016/s0022-510x(02)00358-1. J Neurol Sci. 2003. PMID: 12614925

4

Parkin and endoplasmic reticulum stress.

Takahashi R, Imai Y, Hattori N, Mizuno Y. Takahashi R, et al. Among authors: hattori n. Ann N Y Acad Sci. 2003 Jun;991:101-6. doi: 10.1111/j.1749-6632.2003.tb07467.x. Ann N Y Acad Sci. 2003. PMID: 12846978 Review.

5

Pathogenetic mechanisms of parkin in Parkinson's disease.

Hattori N, Mizuno Y. Hattori N, et al. Lancet. 2004 Aug 21-27;364(9435):722-4. doi: 10.1016/S0140-6736(04)16901-8. Lancet. 2004. PMID: 15325839 Review.

6

Geographic and ethnic differences in frequencies of two polymorphisms (D/N394 and L/I272) of the parkin gene in sporadic Parkinson's disease.

Li X, Kitami T, Wang M, Mizuno Y, Hattori N. Li X, et al. Among authors: hattori n. Parkinsonism Relat Disord. 2005 Dec;11(8):485-91. doi: 10.1016/j.parkreldis.2005.06.006. Epub 2005 Nov 2. Parkinsonism Relat Disord. 2005. PMID: 16269266

7

Recessive Parkinson's disease.

Kubo S, Hattori N, Mizuno Y. Kubo S, et al. Among authors: hattori n. Mov Disord. 2006 Jul;21(7):885-93. doi: 10.1002/mds.20841. Mov Disord. 2006. PMID: 16615060 Review.

8

Twenty years since the discovery of the parkin gene.

Hattori N, Mizuno Y. Hattori N, et al. J Neural Transm (Vienna). 2017 Sep;124(9):1037-1054. doi: 10.1007/s00702-017-1742-7. Epub 2017 Jun 15. J Neural Transm (Vienna). 2017. PMID: 28620835 Review.

9

[Parkin gene and its function; a key to understand nigral degeneration].

Hattori N, Mizuno Y. Hattori N, et al. Rinsho Shinkeigaku. 1999 Dec;39(12):1259-61. Rinsho Shinkeigaku. 1999. PMID: 10791092 Japanese.

10

Genotype-phenotype correlation: familial Parkinson disease.

Mori H, Hattori N, Mizuno Y. Mori H, et al. Among authors: hattori n. Neuropathology. 2003 Mar;23(1):90-4. doi: 10.1046/j.1440-1789.2003.00476.x. Neuropathology. 2003. PMID: 12722931 Review.

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