Takano K - Search Results

1

Germline mosaicism of a novel mutation in lysosome-associated membrane protein-2 deficiency (Danon disease).

Takahashi M, Yamamoto A, Takano K, Sudo A, Wada T, Goto Y, Nishino I, Saitoh S. Takahashi M, et al. Among authors: takano k. Ann Neurol. 2002 Jul;52(1):122-5. doi: 10.1002/ana.10235. Ann Neurol. 2002. PMID: 12112061

2

Cerebellar and brainstem involvement in familial juvenile nephronophthisis type I.

Takano K, Nakamoto T, Okajima M, Sudo A, Uetake K, Saitoh S. Takano K, et al. Pediatr Neurol. 2003 Feb;28(2):142-4. doi: 10.1016/s0887-8994(02)00619-7. Pediatr Neurol. 2003. PMID: 12699867

3

Uniparental disomy and imprinting defects in Japanese patients with Angelman syndrome.

Saitoh S, Wada T, Okajima M, Takano K, Sudo A, Niikawa N. Saitoh S, et al. Among authors: takano k. Brain Dev. 2005 Aug;27(5):389-91. doi: 10.1016/j.braindev.2003.12.013. Brain Dev. 2005. PMID: 16023557

4

Germline mosaicism of a novel UBE3A mutation in Angelman syndrome.

Hosoki K, Takano K, Sudo A, Tanaka S, Saitoh S. Hosoki K, et al. Among authors: takano k. Am J Med Genet A. 2005 Oct 1;138A(2):187-9. doi: 10.1002/ajmg.a.30926. Am J Med Genet A. 2005. PMID: 16100729 No abstract available.

5

DNA demethylation reactivation of imprinted genes in cell lines from patients with Prader-Willi syndrome and a mouse model.

Takano K, Okajima M, Saitoh S. Takano K, et al. Am J Med Genet A. 2007 Jun 15;143A(12):1386-90. doi: 10.1002/ajmg.a.31765. Am J Med Genet A. 2007. PMID: 17506103 No abstract available.

6

High uptake on 11C-methionine positron emission tomographic scan of basal ganglia germinoma with cerebral hemiatrophy.

Sudo A, Shiga T, Okajima M, Takano K, Terae S, Sawamura Y, Ohnishi A, Nagashima K, Saitoh S. Sudo A, et al. Among authors: takano k. AJNR Am J Neuroradiol. 2003 Oct;24(9):1909-11. AJNR Am J Neuroradiol. 2003. PMID: 14561627 Free PMC article.

7

Possible involvement of the tip of temporal lobe in Landau-Kleffner syndrome.

Shiraishi H, Takano K, Shiga T, Okajima M, Sudo A, Asahina N, Kohsaka S, Fukuhara M, Saitoh S. Shiraishi H, et al. Among authors: takano k. Brain Dev. 2007 Sep;29(8):529-33. doi: 10.1016/j.braindev.2007.01.011. Epub 2007 Mar 26. Brain Dev. 2007. PMID: 17383838

8

A three-year-old boy with glucose transporter type 1 deficiency syndrome presenting with episodic ataxia.

Ohshiro-Sasaki A, Shimbo H, Takano K, Wada T, Osaka H. Ohshiro-Sasaki A, et al. Among authors: takano k. Pediatr Neurol. 2014 Jan;50(1):99-100. doi: 10.1016/j.pediatrneurol.2013.09.002. Epub 2013 Nov 5. Pediatr Neurol. 2014. PMID: 24200040

9

Urine screening for patients with developmental disabilities detected a patient with creatine transporter deficiency due to a novel missense mutation in SLC6A8.

Kato H, Miyake F, Shimbo H, Ohya M, Sugawara H, Aida N, Anzai R, Takagi M, Okuda M, Takano K, Wada T, Iai M, Yamashita S, Osaka H. Kato H, et al. Among authors: takano k. Brain Dev. 2014 Aug;36(7):630-3. doi: 10.1016/j.braindev.2013.08.004. Epub 2013 Sep 14. Brain Dev. 2014. PMID: 24045174

10

Idiopathic cranial polyneuropathy with unilateral IX and X and contralateral XI nerve palsy in a 4-year-old boy.

Yoshihara N, Okuda M, Takano K, Wada T, Osaka H. Yoshihara N, et al. Among authors: takano k. Pediatr Neurol. 2012 Sep;47(3):198-200. doi: 10.1016/j.pediatrneurol.2012.04.021. Pediatr Neurol. 2012. PMID: 22883285

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