Morino H - Search Results

1

Middle-age-onset cerebellar ataxia caused by a homozygous TWNK variant: a case report.

Kume K, Morino H, Miyamoto R, Matsuda Y, Ohsawa R, Kanaya Y, Tada Y, Kurashige T, Kawakami H. Kume K, et al. Among authors: morino h. BMC Med Genet. 2020 Mar 31;21(1):68. doi: 10.1186/s12881-020-01002-4. BMC Med Genet. 2020. PMID: 32234020 Free PMC article.

2

Genetic studies in Parkinson's disease with an alpha-synuclein/NACP gene polymorphism in Japan.

Izumi Y, Morino H, Oda M, Maruyama H, Udaka F, Kameyama M, Nakamura S, Kawakami H. Izumi Y, et al. Among authors: morino h. Neurosci Lett. 2001 Mar 9;300(2):125-7. doi: 10.1016/s0304-3940(01)01557-9. Neurosci Lett. 2001. PMID: 11207390

3

Lack of an association between cystatin C gene polymorphisms in Japanese patients with Alzheimer's disease.

Maruyama H, Izumi Y, Oda M, Torii T, Morino H, Toji H, Sasaki K, Terasawa H, Nakamura S, Kawakami H. Maruyama H, et al. Among authors: morino h. Neurology. 2001 Jul 24;57(2):337-9. doi: 10.1212/wnl.57.2.337. Neurology. 2001. PMID: 11468325

4

Dinucleotide repeat polymorphisms in the neprilysin gene are not associated with sporadic Alzheimer's disease.

Oda M, Morino H, Maruyama H, Terasawa H, Izumi Y, Torii T, Sasaki K, Nakamura S, Kawakami H. Oda M, et al. Among authors: morino h. Neurosci Lett. 2002 Mar 1;320(1-2):105-7. doi: 10.1016/s0304-3940(02)00057-5. Neurosci Lett. 2002. PMID: 11849775 Free article.

5

Difference in disease-free survival curve and regional distribution according to subtype of spinocerebellar ataxia: a study of 1,286 Japanese patients.

Maruyama H, Izumi Y, Morino H, Oda M, Toji H, Nakamura S, Kawakami H. Maruyama H, et al. Among authors: morino h. Am J Med Genet. 2002 Jul 8;114(5):578-83. doi: 10.1002/ajmg.10514. Am J Med Genet. 2002. PMID: 12116198

6

Contribution of the interleukin-1beta gene polymorphism in multiple system atrophy.

Nishimura M, Kawakami H, Komure O, Maruyama H, Morino H, Izumi Y, Nakamura S, Kaji R, Kuno S. Nishimura M, et al. Among authors: morino h. Mov Disord. 2002 Jul;17(4):808-11. doi: 10.1002/mds.10124. Mov Disord. 2002. PMID: 12210881

7

SCA8 repeat expansion: large CTA/CTG repeat alleles are more common in ataxic patients, including those with SCA6.

Izumi Y, Maruyama H, Oda M, Morino H, Okada T, Ito H, Sasaki I, Tanaka H, Komure O, Udaka F, Nakamura S, Kawakami H. Izumi Y, et al. Among authors: morino h. Am J Hum Genet. 2003 Mar;72(3):704-9. doi: 10.1086/367775. Epub 2003 Jan 21. Am J Hum Genet. 2003. PMID: 12545428 Free PMC article.

8

Dinucleotide repeat polymorphism in interferon-gamma gene is not associated with sporadic Alzheimer's disease.

Oda M, Maruyama H, Izumi Y, Morino H, Torii T, Nakamura S, Kawakami H. Oda M, et al. Among authors: morino h. Am J Med Genet B Neuropsychiatr Genet. 2004 Jan 1;124B(1):48-9. doi: 10.1002/ajmg.b.20097. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 14681912

9

Possible reduced penetrance of expansion of 44 to 47 CAG/CAA repeats in the TATA-binding protein gene in spinocerebellar ataxia type 17.

Oda M, Maruyama H, Komure O, Morino H, Terasawa H, Izumi Y, Imamura T, Yasuda M, Ichikawa K, Ogawa M, Matsumoto M, Kawakami H. Oda M, et al. Among authors: morino h. Arch Neurol. 2004 Feb;61(2):209-12. doi: 10.1001/archneur.61.2.209. Arch Neurol. 2004. PMID: 14967767

10

A novel haplotype of spinocerebellar ataxia type 6 contributes to the highest prevalence in western Japan.

Terasawa H, Oda M, Morino H, Miyachi T, Izumi Y, Maruyama H, Matsumoto M, Kawakami H. Terasawa H, et al. Among authors: morino h. Neurosci Lett. 2004 Mar 25;358(2):107-10. doi: 10.1016/j.neulet.2004.01.007. Neurosci Lett. 2004. PMID: 15026160

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