Takahashi Y - Search Results

1

Different clinicopathological features between Japanese siblings with facioscapulohumeral muscular dystrophy 2 with a novel nonsense SMCHD1 mutation (Arg552^∗).

Ohta Y, Tadokoro K, Sasaki R, Takahashi Y, Sato K, Takemoto M, Hishikawa N, Shang J, Yamashita T, Takehisa Y, Nishino I, Abe K. Ohta Y, et al. Among authors: takahashi y. J Clin Neurosci. 2018 Dec;58:215-217. doi: 10.1016/j.jocn.2018.10.021. Epub 2018 Oct 13. J Clin Neurosci. 2018. PMID: 30327220

2

A novel mutation of the GAA gene in a patient with adult-onset Pompe disease lacking a disease-specific pathology.

Fujimoto S, Manabe Y, Fujii D, Kozai Y, Matsuzono K, Takahashi Y, Narai H, Omori N, Adachi K, Nanba E, Nishino I, Abe K. Fujimoto S, et al. Among authors: takahashi y. Intern Med. 2013;52(21):2461-4. doi: 10.2169/internalmedicine.52.0311. Intern Med. 2013. PMID: 24190153 Free article.

3

Combined ipsilateral oculomotor nerve palsy and contralateral downbeat nystagmus in a case of cerebral infarction.

Matsuzono K, Manabe Y, Takahashi Y, Narai H, Omori N, Abe K. Matsuzono K, et al. Among authors: takahashi y. Case Rep Neurol. 2014 Apr 30;6(1):134-8. doi: 10.1159/000362120. eCollection 2014 Jan. Case Rep Neurol. 2014. PMID: 24926263 Free PMC article.

4

Serial MR spectroscopy in hypertensive encephalopathy.

Matsubara Y, Manabe Y, Hattori M, Nakano Y, Takahashi Y, Narai H, Ota K, Abe K. Matsubara Y, et al. Among authors: takahashi y. J Neurol Sci. 2014 Dec 15;347(1-2):393-5. doi: 10.1016/j.jns.2014.10.004. Epub 2014 Oct 13. J Neurol Sci. 2014. PMID: 25394908 No abstract available.

5

Estimation of the Presence of Small Dense Lipoprotein Cholesterol in Acute Ischemic Stroke.

Manabe Y, Morihara R, Matsuzono K, Nakano Y, Takahashi Y, Narai H, Omori N, Abe K. Manabe Y, et al. Among authors: takahashi y. Neurol Int. 2015 Jun 3;7(1):5973. doi: 10.4081/ni.2015.5973. eCollection 2015 Mar 23. Neurol Int. 2015. PMID: 26294946 Free PMC article.

6

An AOA2 patient with a novel compound heterozygous SETX frame shift mutations.

Motokura E, Yamashita T, Takahashi Y, Tsunoda K, Sato K, Takemoto M, Hishikawa N, Ohta Y, Hashiguchi A, Takashima H, Abe K. Motokura E, et al. Among authors: takahashi y. J Neurol Sci. 2017 Jan 15;372:294-296. doi: 10.1016/j.jns.2016.11.074. Epub 2016 Nov 30. J Neurol Sci. 2017. PMID: 28017231 No abstract available.

7

A patient with slowly progressive adult-onset nemaline myopathy and novel compound heterozygous mutations in the nebulin gene.

Tsunoda K, Yamashita T, Motokura E, Takahashi Y, Sato K, Takemoto M, Hishikawa N, Ohta Y, Nishikawa A, Nishino I, Abe K. Tsunoda K, et al. Among authors: takahashi y. J Neurol Sci. 2017 Feb 15;373:254-257. doi: 10.1016/j.jns.2016.12.069. Epub 2016 Dec 30. J Neurol Sci. 2017. PMID: 28131200 No abstract available.

8

A case of seropositive autoimmune autonomic ganglionopathy with diffuse esophageal spasm.

Morimoto N, Takahashi S, Inaba T, Takamiya M, Kageyama Y, Morimoto M, Takahashi Y, Nishimura H, Nakane S, Abe K. Morimoto N, et al. Among authors: takahashi y, takahashi s. J Clin Neurosci. 2017 May;39:90-92. doi: 10.1016/j.jocn.2017.01.027. Epub 2017 Feb 14. J Clin Neurosci. 2017. PMID: 28214088

9

Different Characteristics of Anterior and Posterior Branch Atheromatous Diseases with or without Early Neurologic Deterioration.

Takahashi Y, Yamashita T, Morihara R, Nakano Y, Sato K, Takemoto M, Hishikawa N, Ohta Y, Manabe Y, Abe K. Takahashi Y, et al. J Stroke Cerebrovasc Dis. 2017 Jun;26(6):1314-1320. doi: 10.1016/j.jstrokecerebrovasdis.2017.02.001. Epub 2017 Mar 29. J Stroke Cerebrovasc Dis. 2017. PMID: 28365073

10

Parkinsonism in Association with Dihydropteridine Reductase Deficiency.

Takahashi Y, Manabe Y, Nakano Y, Yunoki T, Kono S, Narai H, Furujo M, Abe K. Takahashi Y, et al. Case Rep Neurol. 2017 Feb 14;9(1):17-21. doi: 10.1159/000456610. eCollection 2017 Jan-Apr. Case Rep Neurol. 2017. PMID: 28413401 Free PMC article.

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