Ujike H - Search Results

1

Familial amyotrophic lateral sclerosis with a novel Leu126Ser mutation in the copper/zinc superoxide dismutase gene showing mild clinical features and lewy body-like hyaline inclusions.

Takehisa Y, Ujike H, Ishizu H, Terada S, Haraguchi T, Tanaka Y, Nishinaka T, Nobukuni K, Ihara Y, Namba R, Yasuda T, Nishibori M, Hayabara T, Kuroda S. Takehisa Y, et al. Among authors: ujike h. Arch Neurol. 2001 May;58(5):736-40. doi: 10.1001/archneur.58.5.736. Arch Neurol. 2001. PMID: 11346368

2

A family with X-linked dystonia-deafness syndrome with a novel mutation of the DDP gene.

Ujike H, Tanabe Y, Takehisa Y, Hayabara T, Kuroda S. Ujike H, et al. Arch Neurol. 2001 Jun;58(6):1004-7. doi: 10.1001/archneur.58.6.1004. Arch Neurol. 2001. PMID: 11405816 Review.

3

Lewy body variant of Alzheimer's disease or cerebral type lewy body disease? Two autopsy cases of presenile onset with minimal involvement of the brainstem.

Yokota O, Tsuchiya K, Uchihara T, Ujike H, Terada S, Takahashi M, Kimura Y, Ishizu H, Akiyama H, Kuroda S. Yokota O, et al. Among authors: ujike h. Neuropathology. 2007 Feb;27(1):21-35. doi: 10.1111/j.1440-1789.2006.00736.x. Neuropathology. 2007. PMID: 17319280

4

NACP/alpha-synuclein, NAC, and beta-amyloid pathology of familial Alzheimer's disease with the E184D presenilin-1 mutation: a clinicopathological study of two autopsy cases.

Yokota O, Terada S, Ishizu H, Ujike H, Ishihara T, Nakashima H, Yasuda M, Kitamura Y, Uéda K, Checler F, Kuroda S. Yokota O, et al. Among authors: ujike h. Acta Neuropathol. 2002 Dec;104(6):637-48. doi: 10.1007/s00401-002-0596-7. Epub 2002 Aug 14. Acta Neuropathol. 2002. PMID: 12410385

5

Variability and heterogeneity in Alzheimer's disease with cotton wool plaques: a clinicopathological study of four autopsy cases.

Yokota O, Terada S, Ishizu H, Ujike H, Ishihara T, Namba M, Hayashi Y, Nishinaka T, Namba R, Nakashima H, Uéda K, Checler F, Kuroda S. Yokota O, et al. Among authors: ujike h. Acta Neuropathol. 2003 Oct;106(4):348-56. doi: 10.1007/s00401-003-0737-7. Epub 2003 Jul 16. Acta Neuropathol. 2003. PMID: 12883830

6

Schizophrenic psychoses and the CNTF null mutation.

Tanaka Y, Ujike H, Fujiwara Y, Takeda T, Takehisa Y, Kodama M, Otsuki S, Kuroda S. Tanaka Y, et al. Among authors: ujike h. Neuroreport. 1998 Apr 20;9(6):981-3. doi: 10.1097/00001756-199804200-00005. Neuroreport. 1998. PMID: 9601653 Clinical Trial.

7

NOTCH4 gene polymorphism and susceptibility to schizophrenia and schizoaffective disorder.

Ujike H, Takehisa Y, Takaki M, Tanaka Y, Nakata K, Takeda T, Kodama M, Fujiwara Y, Yamamoto A, Kuroda S. Ujike H, et al. Neurosci Lett. 2001 Mar 23;301(1):41-4. doi: 10.1016/s0304-3940(01)01602-0. Neurosci Lett. 2001. PMID: 11239712

8

Association study of CAG repeats in the KCNN3 gene in Japanese patients with schizophrenia, schizoaffective disorder and bipolar disorder.

Ujike H, Yamamoto A, Tanaka Y, Takehisa Y, Takaki M, Taked T, Kodama M, Kuroda S. Ujike H, et al. Psychiatry Res. 2001 Apr 15;101(3):203-7. doi: 10.1016/s0165-1781(01)00229-3. Psychiatry Res. 2001. PMID: 11311923

9

Two kinds of mitogen-activated protein kinase phosphatases, MKP-1 and MKP-3, are differentially activated by acute and chronic methamphetamine treatment in the rat brain.

Takaki M, Ujike H, Kodama M, Takehisa Y, Nakata K, Kuroda S. Takaki M, et al. Among authors: ujike h. J Neurochem. 2001 Nov;79(3):679-88. doi: 10.1046/j.1471-4159.2001.00615.x. J Neurochem. 2001. PMID: 11701771 Free article.

10

[Diffuse reduced uptake in 99m-Tc-HM-PAO SPECT and high level of neuron-specific enolase in cerebrospinal fluid in the early stage of Creutzfeldt-Jakob disease].

Kohira I, Ishizu H, Shohmori T, Ujike H, Kuroda S, Otsuki S, Ihara Y. Kohira I, et al. Among authors: ujike h. No To Shinkei. 1992 Jun;44(6):579-82. No To Shinkei. 1992. PMID: 1389566 Japanese.

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