Miyajima H - Search Results

1

T2* and FSE MRI distinguishes four subtypes of neurodegeneration with brain iron accumulation.

McNeill A, Birchall D, Hayflick SJ, Gregory A, Schenk JF, Zimmerman EA, Shang H, Miyajima H, Chinnery PF. McNeill A, et al. Among authors: miyajima h. Neurology. 2008 Apr 29;70(18):1614-9. doi: 10.1212/01.wnl.0000310985.40011.d6. Neurology. 2008. PMID: 18443312 Free PMC article.

2

The neurological presentation of ceruloplasmin gene mutations.

McNeill A, Pandolfo M, Kuhn J, Shang H, Miyajima H. McNeill A, et al. Among authors: miyajima h. Eur Neurol. 2008;60(4):200-5. doi: 10.1159/000148691. Epub 2008 Jul 30. Eur Neurol. 2008. PMID: 18667828 Review.

3

Brain and liver iron accumulation in aceruloplasminemia.

Fujita K, Osaki Y, Harada M, Kono S, Miyajima H, Izumi Y, Kaji R. Fujita K, et al. Among authors: miyajima h. Neurology. 2013 Dec 10;81(24):2145-6. doi: 10.1212/01.wnl.0000437304.30227.bd. Neurology. 2013. PMID: 24323439 No abstract available.

4

Olfactory impairment and pathology in neurodegenerative disorders with brain iron accumulation.

Dziewulska D, Doi H, Fasano A, Erro R, Fatehi F, Fekete R, Gatto EM, Pablos EG, Lehn A, Miyajima H, Piperno A, Pellechia MT, Wu YR, Yoshida K, Zarruk JG, Jingli S, Schrag A, McNeill A. Dziewulska D, et al. Among authors: miyajima h. Acta Neuropathol. 2013 Jul;126(1):151-3. doi: 10.1007/s00401-013-1136-3. Epub 2013 May 31. Acta Neuropathol. 2013. PMID: 23722254 No abstract available.

5

[An autopsy case of multiple system atrophy with a heteroallelic ceruloplasmin gene mutation].

Yomono H, Kurisaki H, Murayama S, Hebisawa A, Miyajima H, Takahashi Y. Yomono H, et al. Among authors: miyajima h. Rinsho Shinkeigaku. 2003 Jul;43(7):398-402. Rinsho Shinkeigaku. 2003. PMID: 14582365 Japanese.

6

CSF abnormalities in patients with aceruloplasminemia.

Miyajima H, Fujimoto M, Kohno S, Kaneko E, Gitlin JD. Miyajima H, et al. Neurology. 1998 Oct;51(4):1188-90. doi: 10.1212/wnl.51.4.1188. Neurology. 1998. PMID: 9781556

7

Cerebellar ataxia associated with heteroallelic ceruloplasmin gene mutation.

Miyajima H, Kono S, Takahashi Y, Sugimoto M, Sakamoto M, Sakai N. Miyajima H, et al. Neurology. 2001 Dec 26;57(12):2205-10. doi: 10.1212/wnl.57.12.2205. Neurology. 2001. PMID: 11756598

8

Multiple motor system dysfunction associated with a heterozygous ceruloplasmin gene mutation.

Jiménez-Huete A, Bernar J, Miyajima H, Takahashi Y, Alvarez-Linera J, Franch O, van der Knaap MS. Jiménez-Huete A, et al. Among authors: miyajima h. J Neurol. 2008 Jul;255(7):1083-4. doi: 10.1007/s00415-008-0823-9. Epub 2008 Feb 25. J Neurol. 2008. PMID: 18293024 No abstract available.

9

A case of aceruloplasminaemia: abnormal serum ceruloplasmin protein without ferroxidase activity.

Takeuchi Y, Yoshikawa M, Tsujino T, Kohno S, Tsukamoto N, Shiroi A, Kikuchi E, Fukui H, Miyajima H. Takeuchi Y, et al. Among authors: miyajima h. J Neurol Neurosurg Psychiatry. 2002 Apr;72(4):543-5. doi: 10.1136/jnnp.72.4.543. J Neurol Neurosurg Psychiatry. 2002. PMID: 11909923 Free PMC article.

10

Extrapyramidal and cerebellar movement disorder in association with heterozygous ceruloplasmin gene mutation.

Kuhn J, Miyajima H, Takahashi Y, Kunath B, Hartmann-Klosterkoetter U, Cooper-Mahkorn D, Schaefer M, Bewermeyer H. Kuhn J, et al. Among authors: miyajima h. J Neurol. 2005 Jan;252(1):111-3. doi: 10.1007/s00415-005-0608-3. J Neurol. 2005. PMID: 15654567 No abstract available.

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