Ishikawa A - Search Results

1

An autopsy case of autosomal-recessive juvenile parkinsonism with a homozygous exon 4 deletion in the parkin gene.

Hayashi S, Wakabayashi K, Ishikawa A, Nagai H, Saito M, Maruyama M, Takahashi T, Ozawa T, Tsuji S, Takahashi H. Hayashi S, et al. Among authors: ishikawa a. Mov Disord. 2000 Sep;15(5):884-8. doi: 10.1002/1531-8257(200009)15:5<884::aid-mds1019>3.0.co;2-8. Mov Disord. 2000. PMID: 11009195

2

Familial juvenile parkinsonism: clinical and pathologic study in a family.

Takahashi H, Ohama E, Suzuki S, Horikawa Y, Ishikawa A, Morita T, Tsuji S, Ikuta F. Takahashi H, et al. Among authors: ishikawa a. Neurology. 1994 Mar;44(3 Pt 1):437-41. doi: 10.1212/wnl.44.3_part_1.437. Neurology. 1994. PMID: 8145912

3

Clinical analysis of 17 patients in 12 Japanese families with autosomal-recessive type juvenile parkinsonism.

Ishikawa A, Tsuji S. Ishikawa A, et al. Neurology. 1996 Jul;47(1):160-6. doi: 10.1212/wnl.47.1.160. Neurology. 1996. PMID: 8710071

4

Autosomal dominant diffuse Lewy body disease.

Wakabayashi K, Hayashi S, Ishikawa A, Hayashi T, Okuizumi K, Tanaka H, Tsuji S, Takahashi H. Wakabayashi K, et al. Among authors: ishikawa a. Acta Neuropathol. 1998 Aug;96(2):207-10. doi: 10.1007/s004010050883. Acta Neuropathol. 1998. PMID: 9705138

5

Novel mutations, pseudo-dominant inheritance, and possible familial affects in patients with autosomal recessive juvenile parkinsonism.

Maruyama M, Ikeuchi T, Saito M, Ishikawa A, Yuasa T, Tanaka H, Hayashi S, Wakabayashi K, Takahashi H, Tsuji S. Maruyama M, et al. Among authors: ishikawa a. Ann Neurol. 2000 Aug;48(2):245-50. Ann Neurol. 2000. PMID: 10939576

6

Autosomal recessive juvenile parkinsonism.

Saito M, Maruyama M, Ikeuchi K, Kondo H, Ishikawa A, Yuasa T, Tsuji S. Saito M, et al. Among authors: ishikawa a. Brain Dev. 2000 Sep;22 Suppl 1:S115-7. doi: 10.1016/s0387-7604(00)00137-6. Brain Dev. 2000. PMID: 10984671 Review.

7

Refinement of the gene locus for autosomal recessive juvenile parkinsonism (AR-JP) on chromosome 6q25.2-27 and identification of markers exhibiting linkage disequilibrium.

Saito M, Matsumine H, Tanaka H, Ishikawa A, Shimoda-Matsubayashi S, Schäffer AA, Mizuno Y, Tsuji S. Saito M, et al. Among authors: ishikawa a. J Hum Genet. 1998;43(1):22-31. doi: 10.1007/s100380050032. J Hum Genet. 1998. PMID: 9609994

8

Patients homozygous and heterozygous for SNCA duplication in a family with parkinsonism and dementia.

Ikeuchi T, Kakita A, Shiga A, Kasuga K, Kaneko H, Tan CF, Idezuka J, Wakabayashi K, Onodera O, Iwatsubo T, Nishizawa M, Takahashi H, Ishikawa A. Ikeuchi T, et al. Among authors: ishikawa a. Arch Neurol. 2008 Apr;65(4):514-9. doi: 10.1001/archneur.65.4.514. Arch Neurol. 2008. PMID: 18413475

9

Genetic Variations and Neuropathologic Features of Patients with PRKN Mutations.

Seike N, Yokoseki A, Takeuchi R, Saito K, Miyahara H, Miyashita A, Ikeda T, Aida I, Nakajima T, Kanazawa M, Wakabayashi M, Toyoshima Y, Takahashi H, Matsumoto R, Toda T, Onodera O, Ishikawa A, Ikeuchi T, Kakita A. Seike N, et al. Among authors: ishikawa a. Mov Disord. 2021 Jul;36(7):1634-1643. doi: 10.1002/mds.28521. Epub 2021 Feb 11. Mov Disord. 2021. PMID: 33570211

10

Linkage analysis of juvenile parkinsonism to tyrosine hydroxylase gene locus on chromosome 11.

Tanaka H, Ishikawa A, Ginns EI, Miyatake T, Tsuji S. Tanaka H, et al. Among authors: ishikawa a. Neurology. 1991 May;41(5):719-22. doi: 10.1212/wnl.41.5.719. Neurology. 1991. PMID: 1674118

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