Maruyama H - Search Results

1

LRRK2 mutations and risk variants in Japanese patients with Parkinson's disease.

Zabetian CP, Yamamoto M, Lopez AN, Ujike H, Mata IF, Izumi Y, Kaji R, Maruyama H, Morino H, Oda M, Hutter CM, Edwards KL, Schellenberg GD, Tsuang DW, Yearout D, Larson EB, Kawakami H. Zabetian CP, et al. Among authors: maruyama h. Mov Disord. 2009 May 15;24(7):1034-41. doi: 10.1002/mds.22514. Mov Disord. 2009. PMID: 19343804 Free PMC article.

2

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: maruyama h. Neurology. 1996 Apr;46(4):1154-6. doi: 10.1212/wnl.46.4.1154. Neurology. 1996. PMID: 8780110

3

[Molecular genetics of Machado-Joseph disease].

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

4

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: maruyama h. Neurosci Lett. 1999 Jan 4;259(1):56-8. doi: 10.1016/s0304-3940(98)00855-6. Neurosci Lett. 1999. PMID: 10027555

5

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: maruyama h. Neurosci Lett. 2001 Mar 9;300(2):125-7. doi: 10.1016/s0304-3940(01)01557-9. Neurosci Lett. 2001. PMID: 11207390

6

[Spinocerebellar ataxia type 8(SCA 8)].

Izumi Y, Maruyama H, Kawakami H. Izumi Y, et al. Among authors: maruyama h. No To Shinkei. 2001 Jan;53(1):34-40. No To Shinkei. 2001. PMID: 11211728 Review. Japanese. No abstract available.

7

Influence of interleukin-1beta gene polymorphism on age-at-onset of spinocerebellar ataxia 6 (SCA6) in Japanese patients.

Nishimura M, Kawakami H, Maruyama H, Izumi Y, Kuno S, Kaji R, Nakamura S. Nishimura M, et al. Among authors: maruyama h. Neurosci Lett. 2001 Jul 13;307(2):128-30. doi: 10.1016/s0304-3940(01)01934-6. Neurosci Lett. 2001. PMID: 11427317

8

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. Neurology. 2001 Jul 24;57(2):337-9. doi: 10.1212/wnl.57.2.337. Neurology. 2001. PMID: 11468325

9

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: maruyama 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.

10

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. Am J Med Genet. 2002 Jul 8;114(5):578-83. doi: 10.1002/ajmg.10514. Am J Med Genet. 2002. PMID: 12116198

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