Ikeuchi T - Search Results

1

Pathological Progression Induced by the Frontotemporal Dementia-Associated R406W Tau Mutation in Patient-Derived iPSCs.

Nakamura M, Shiozawa S, Tsuboi D, Amano M, Watanabe H, Maeda S, Kimura T, Yoshimatsu S, Kisa F, Karch CM, Miyasaka T, Takashima A, Sahara N, Hisanaga SI, Ikeuchi T, Kaibuchi K, Okano H. Nakamura M, et al. Among authors: ikeuchi t. Stem Cell Reports. 2019 Oct 8;13(4):684-699. doi: 10.1016/j.stemcr.2019.08.011. Epub 2019 Sep 19. Stem Cell Reports. 2019. PMID: 31543469 Free PMC article.

2

Different AT(N) profiles and clinical progression classified by two different N markers using total tau and neurofilament light chain in cerebrospinal fluid.

Kasuga K, Kikuchi M, Tsukie T, Suzuki K, Ihara R, Iwata A, Hara N, Miyashita A, Kuwano R, Iwatsubo T, Ikeuchi T; Japanese Alzheimer’s Disease Neuroimaging Initiative. Kasuga K, et al. Among authors: ikeuchi t. BMJ Neurol Open. 2022 Aug 10;4(2):e000321. doi: 10.1136/bmjno-2022-000321. eCollection 2022. BMJ Neurol Open. 2022. PMID: 36046332 Free PMC article.

3

[Progression of cluster headache to Raeder's syndrome with marked response to corticosteroid therapy: a case report].

Ikeuchi T, Tokutake T, Sakamaki Y, Takagi M, Nishizawa M. Ikeuchi T, et al. Rinsho Shinkeigaku. 2005 Apr;45(4):321-3. Rinsho Shinkeigaku. 2005. PMID: 15912803 Japanese.

4

Partial 18q trisomy and 18p monosomy resulting from a maternal pericentric inversion, inv(18)(p11.2q21.3).

Asano T, Ikeuchi T, Shinohara T, Enokido H, Hashimoto K. Asano T, et al. Among authors: ikeuchi t. Jinrui Idengaku Zasshi. 1991 Sep;36(3):257-65. doi: 10.1007/BF01910544. Jinrui Idengaku Zasshi. 1991. PMID: 1753439 Review.

5

A Novel Hypomorphic CSF1R Gene Mutation in the Biallelic State Leading to Fatal Childhood Neurodegeneration.

Tamhankar PM, Zhu B, Tamhankar VP, Mithbawkar S, Seabra L, Livingston JH, Ikeuchi T, Crow YJ. Tamhankar PM, et al. Among authors: ikeuchi t. Neuropediatrics. 2020 Aug;51(4):302-306. doi: 10.1055/s-0040-1702161. Epub 2020 May 28. Neuropediatrics. 2020. PMID: 32464672

6

Adult-onset leukoencephalopathy with axonal spheroids and pigmental glia with diffuse cerebral microbleeds: case report.

Ishikawa R, Wada K, Ikeuchi T. Ishikawa R, et al. Among authors: ikeuchi t. Acta Neurol Belg. 2023 Apr;123(2):739-741. doi: 10.1007/s13760-022-02110-z. Epub 2022 Oct 7. Acta Neurol Belg. 2023. PMID: 36207627 No abstract available.

7

Distal trisomy of chromosome 17q due to inverted tandem duplication.

Shimizu T, Ikeuchi T, Shinohara T, Ohba S, Miyaguchi H, Akiyama T, Shibata T. Shimizu T, et al. Among authors: ikeuchi t. Clin Genet. 1988 Apr;33(4):311-4. doi: 10.1111/j.1399-0004.1988.tb03454.x. Clin Genet. 1988. PMID: 3359688

8

Localization at a subband level of polymorphic 13q14 DNA probes for diagnosis of hereditary retinoblastoma and Wilson disease.

Scheffer H, Kema IP, Kondo I, van der Veen AY, Ikeuchi T, Buys CH. Scheffer H, et al. Among authors: ikeuchi t. Hum Genet. 1987 Dec;77(4):335-7. doi: 10.1007/BF00291421. Hum Genet. 1987. PMID: 2891602

9

Trisomy 9p due to a maternal complex translocation involving chromosomes 4, 6 and 9.

Tanaka N, Ikeuchi T, Yara I, Kitahara K. Tanaka N, et al. Among authors: ikeuchi t. Jinrui Idengaku Zasshi. 1977 Mar;21(4):261-8. Jinrui Idengaku Zasshi. 1977. PMID: 559818 No abstract available.

10

Unbalanced 13q/21q translocation: a revised study of the case previously reported as 21-monosomy.

Ikeuchi T, Kondo I, Sasaki M, Kaneko Y, Kodama S. Ikeuchi T, et al. Hum Genet. 1976 Aug 30;33(3):327-30. doi: 10.1007/BF00286861. Hum Genet. 1976. PMID: 964993

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