Kawakami H - Search Results

1

Cerebellar ataxia with SYNE1 mutation accompanying motor neuron disease.

Izumi Y, Miyamoto R, Morino H, Yoshizawa A, Nishinaka K, Udaka F, Kameyama M, Maruyama H, Kawakami H. Izumi Y, et al. Among authors: kawakami h. Neurology. 2013 Feb 5;80(6):600-1. doi: 10.1212/WNL.0b013e3182815529. Epub 2013 Jan 16. Neurology. 2013. PMID: 23325900 No abstract available.

2

Reevaluation of the exact CAG repeat length in hereditary cerebellar ataxias using highly denaturing conditions and long PCR.

Maruyama H, Kawakami H, Nakamura S. Maruyama H, et al. Among authors: kawakami h. Hum Genet. 1996 May;97(5):591-5. doi: 10.1007/BF02281866. Hum Genet. 1996. PMID: 8655136

3

A family with Machado-Joseph disease, previously diagnosed as dentatorubral-pallidoluysian atrophy.

Sakai T, Antoku Y, Kawakami H, Maruyama H, Nakamura S, Tanaka K. Sakai T, et al. Among authors: kawakami h. Neurology. 1996 Apr;46(4):1154-6. doi: 10.1212/wnl.46.4.1154. Neurology. 1996. PMID: 8780110

4

[Molecular genetics of Machado-Joseph disease].

Kawakami H, Maruyama H, Nakamura S. Kawakami H, et al. Nihon Rinsho. 1996 Mar;54(3):854-60. Nihon Rinsho. 1996. PMID: 8904248 Review. Japanese.

5

Homozygosity for an allele carrying intermediate CAG repeats in the dentatorubral-pallidoluysian atrophy (DRPLA) gene results in spastic paraplegia.

Kurohara K, Kuroda Y, Maruyama H, Kawakami H, Yukitake M, Matsui M, Nakamura S. Kurohara K, et al. Among authors: kawakami h. Neurology. 1997 Apr;48(4):1087-90. doi: 10.1212/wnl.48.4.1087. Neurology. 1997. PMID: 9109905

6

Molecular features of the CAG repeats of spinocerebellar ataxia 6 (SCA6).

Matsuyama Z, Kawakami H, Maruyama H, Izumi Y, Komure O, Udaka F, Kameyama M, Nishio T, Kuroda Y, Nishimura M, Nakamura S. Matsuyama Z, et al. Among authors: kawakami h. Hum Mol Genet. 1997 Aug;6(8):1283-7. doi: 10.1093/hmg/6.8.1283. Hum Mol Genet. 1997. PMID: 9259274

7

A new mitochondrial DNA mutation associated with mitochondrial myopathy: tRNA(Leu)(UUR) 3254C-to-G.

Kawarai T, Kawakami H, Kozuka K, Izumi Y, Matsuyama Z, Watanabe C, Kohriyama T, Nakamura S. Kawarai T, et al. Among authors: kawakami h. Neurology. 1997 Aug;49(2):598-600. doi: 10.1212/wnl.49.2.598. Neurology. 1997. PMID: 9270605

8

Characteristic magnetic resonance imaging findings in Machado-Joseph disease.

Murata Y, Yamaguchi S, Kawakami H, Imon Y, Maruyama H, Sakai T, Kazuta T, Ohtake T, Nishimura M, Saida T, Chiba S, Oh-i T, Nakamura S. Murata Y, et al. Among authors: kawakami h. Arch Neurol. 1998 Jan;55(1):33-7. doi: 10.1001/archneur.55.1.33. Arch Neurol. 1998. PMID: 9443709

9

Apolipoprotein E promoter polymorphism and sporadic Alzheimer's disease in a Japanese population.

Toji H, Maruyama H, Sasaki K, Nakamura S, Kawakami H. Toji H, et al. Among authors: kawakami h. Neurosci Lett. 1999 Jan 4;259(1):56-8. doi: 10.1016/s0304-3940(98)00855-6. Neurosci Lett. 1999. PMID: 10027555

10

[A sporadic case of spinocerebellar ataxia 6 (SCA 6) with large CAG expansion of the CACNL1A4 gene].

Izumi Y, Sawada H, Matsuyama Z, Kawakami H, Udaka F, Nakamura S, Kameyama M. Izumi Y, et al. Among authors: kawakami h. No To Shinkei. 1999 Feb;51(2):167-70. No To Shinkei. 1999. PMID: 10198907 Japanese.

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