Hattori N - Search Results

1

[A 62-year-old woman with early-onset Parkinson's disease associated with the PINKi gene deletion].

Atsumi M, Li Y, Tomiyama H, Sato K, Hattori N. Atsumi M, et al. Among authors: hattori n. Rinsho Shinkeigaku. 2006 Mar;46(3):199-202. Rinsho Shinkeigaku. 2006. PMID: 16642930 Japanese.

2

[A 56-year-old woman with parkinsonism and dementia with the age of onset at 41 years].

Hattori N, Sugano K, Wakiya M, Mori H, Shirai T, Mizuno Y. Hattori N, et al. No To Shinkei. 1995 Sep;47(9):911-9. No To Shinkei. 1995. PMID: 7546942 Japanese.

3

[A patient with focal bi-parietal atrophy presenting motor clumsiness and cortical sensory loss].

Sato S, Hattori N, Matsumine H, Imai H, Mizuno Y. Sato S, et al. Among authors: hattori n. Rinsho Shinkeigaku. 1998 Mar;38(3):246-51. Rinsho Shinkeigaku. 1998. PMID: 9711123 Review. Japanese.

4

[A 74-year-old woman with parkinsonism and dementia who died four years after the onset].

Okuma Y, Hattori N, Nobukawa B, Mori H, Suda K, Takubo H, Mizuno Y. Okuma Y, et al. Among authors: hattori n. No To Shinkei. 1998 Jul;50(7):671-82. No To Shinkei. 1998. PMID: 9739528 Japanese.

5

Polymorphism in the parkin gene in sporadic Parkinson's disease.

Wang M, Hattori N, Matsumine H, Kobayashi T, Yoshino H, Morioka A, Kitada T, Asakawa S, Minoshima S, Shimizu N, Mizuno Y. Wang M, et al. Among authors: hattori n. Ann Neurol. 1999 May;45(5):655-8. doi: 10.1002/1531-8249(199905)45:5<655::aid-ana15>3.0.co;2-g. Ann Neurol. 1999. PMID: 10319889

6

[An 80-year-old woman with parkinsonism and progressive dementia].

Hattori N, Sumino S, Takanashi M, Mori H, Wakiya M, Shirai T, Sugita H, Mizuno Y. Hattori N, et al. No To Shinkei. 1999 Jun;51(6):541-50. No To Shinkei. 1999. PMID: 10423759 Japanese.

7

[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.

8

[Two families of Charcot-Marie-Tooth disease with Adie's pupil, axonal neuropahy and the Thr124Met mutation in the peripheral myelin protein zero gene].

Misu K, Yoshihara T, Yamamoto M, Hattori N, Nagamatu M, Mukai E, Takegami T, Sobue G. Misu K, et al. Among authors: hattori n. Rinsho Shinkeigaku. 2000 Feb;40(2):149-54. Rinsho Shinkeigaku. 2000. PMID: 10835936 Japanese.

9

[A case of spinal muscular atrophy with marked calf hypertrophy and adolescent onset].

Hattori N, Nishigaki T, Inui K, Kaido M, Nishimura T, Hazama T, Nakata T. Hattori N, et al. Rinsho Shinkeigaku. 2000 Feb;40(2):170-3. Rinsho Shinkeigaku. 2000. PMID: 10835940 Japanese.

10

[Malignant migraine].

Sato K, Hattori N, Mizuno Y. Sato K, et al. Among authors: hattori n. Nihon Rinsho. 2002 Apr;60 Suppl 4:278-81. Nihon Rinsho. 2002. PMID: 12013865 Review. Japanese. No abstract available.

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