Kasuga K - Search Results

1

Increased levels of soluble LR11 in cerebrospinal fluid of patients with Alzheimer disease.

Ikeuchi T, Hirayama S, Miida T, Fukamachi I, Tokutake T, Ebinuma H, Takubo K, Kaneko H, Kasuga K, Kakita A, Takahashi H, Bujo H, Saito Y, Nishizawa M. Ikeuchi T, et al. Among authors: kasuga k. Dement Geriatr Cogn Disord. 2010;30(1):28-32. doi: 10.1159/000315539. Epub 2010 Jul 30. Dement Geriatr Cogn Disord. 2010. PMID: 20689279

2

[Recent progress in genetic study of hereditary spastic paraplegia].

Takano H, Kasuga K, Kobayashi H, Nishizawa M. Takano H, et al. Among authors: kasuga k. No To Shinkei. 2003 Sep;55(9):757-63. No To Shinkei. 2003. PMID: 14571837 Review. Japanese. No abstract available.

3

[Hereditary spastic paraplegia associated with thin corpus callosum].

Kasuga K, Nishizawa M. Kasuga K, et al. No To Shinkei. 2003 Sep;55(9):765-70. No To Shinkei. 2003. PMID: 14571838 Review. Japanese. No abstract available.

4

[A case with severe respiratory muscle weakness due to chronic myositis associated with PBC].

Kasuga K, Sato A, Kanazawa M, Kobayashi H, Tanaka K, Nishizawa M. Kasuga K, et al. Rinsho Shinkeigaku. 2004 Apr-May;44(4-5):280-5. Rinsho Shinkeigaku. 2004. PMID: 15287510 Japanese.

5

Novel locus for benign hereditary chorea with adult onset maps to chromosome 8q21.3 q23.3.

Shimohata T, Hara K, Sanpei K, Nunomura J, Maeda T, Kawachi I, Kanazawa M, Kasuga K, Miyashita A, Kuwano R, Hirota K, Tsuji S, Onodera O, Nishizawa M, Honma Y. Shimohata T, et al. Among authors: kasuga k. Brain. 2007 Sep;130(Pt 9):2302-9. doi: 10.1093/brain/awm036. Epub 2007 Apr 2. Brain. 2007. PMID: 17405764

6

Generation of intracellular domain of insulin receptor tyrosine kinase by gamma-secretase.

Kasuga K, Kaneko H, Nishizawa M, Onodera O, Ikeuchi T. Kasuga K, et al. Biochem Biophys Res Commun. 2007 Aug 17;360(1):90-6. doi: 10.1016/j.bbrc.2007.06.022. Epub 2007 Jun 12. Biochem Biophys Res Commun. 2007. PMID: 17577576

7

Chronic myositis with cardiomyopathy and respiratory failure associated with mild form of organ-specific autoimmune diseases.

Tanaka K, Sato A, Kasuga K, Kanazawa M, Yanagawa K, Umeda M, Tada M, Tanaka M, Nishizawa M. Tanaka K, et al. Among authors: kasuga k. Clin Rheumatol. 2007 Nov;26(11):1917-9. doi: 10.1007/s10067-007-0698-7. Epub 2007 Aug 3. Clin Rheumatol. 2007. PMID: 17674117

8

Enhanced accumulation of phosphorylated alpha-synuclein and elevated beta-amyloid 42/40 ratio caused by expression of the presenilin-1 deltaT440 mutant associated with familial Lewy body disease and variant Alzheimer's disease.

Kaneko H, Kakita A, Kasuga K, Nozaki H, Ishikawa A, Miyashita A, Kuwano R, Ito G, Iwatsubo T, Takahashi H, Nishizawa M, Onodera O, Sisodia SS, Ikeuchi T. Kaneko H, et al. Among authors: kasuga k. J Neurosci. 2007 Nov 28;27(48):13092-7. doi: 10.1523/JNEUROSCI.4244-07.2007. J Neurosci. 2007. PMID: 18045903 Free PMC article.

9

Patients homozygous and heterozygous for SNCA duplication in a family with parkinsonism and dementia.

Ikeuchi T, Kakita A, Shiga A, Kasuga K, Kaneko H, Tan CF, Idezuka J, Wakabayashi K, Onodera O, Iwatsubo T, Nishizawa M, Takahashi H, Ishikawa A. Ikeuchi T, et al. Among authors: kasuga k. Arch Neurol. 2008 Apr;65(4):514-9. doi: 10.1001/archneur.65.4.514. Arch Neurol. 2008. PMID: 18413475

10

Mutational analysis in early-onset familial dementia in the Japanese population. The role of PSEN1 and MAPT R406W mutations.

Ikeuchi T, Kaneko H, Miyashita A, Nozaki H, Kasuga K, Tsukie T, Tsuchiya M, Imamura T, Ishizu H, Aoki K, Ishikawa A, Onodera O, Kuwano R, Nishizawa M. Ikeuchi T, et al. Among authors: kasuga k. Dement Geriatr Cogn Disord. 2008;26(1):43-9. doi: 10.1159/000141483. Epub 2008 Jun 28. Dement Geriatr Cogn Disord. 2008. PMID: 18587238

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