Extrapyramidal and cerebellar movement disorder in association with heterozygous ceruloplasmin gene mutation-Reference-Cited by-同舟云学术

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

Published:2005-01 Issue:1 Volume:252 Page:111-113
ISSN:0340-5354
Container-title:Journal of Neurology
language:en
Short-container-title:J Neurol

Author:

Kuhn Jens,Miyajima Hiroaki,Takahashi Yoshitomo,Kunath Bernhard,Hartmann-Klosterkoetter Ursula,Cooper-Mahkorn D�irdre,Schaefer Mark,Bewermeyer Heiko

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical),Neurology

Link

http://link.springer.com/content/pdf/10.1007/s00415-005-0608-3.pdf

Reference13 articles.

1. Daimon M, Moriai S, Susa S, Yamatani K, Hosoya T, Kato T (1999) Hypocaeruloplasminaemia with heteroallelic caeruloplasmin gene mutation: MRI of the brain. Neuroradiology 41:185?187

2. Daimon M, Susa S, Ohizumi, T, Moriai S, Kawanami T, Hirata A, Yamaguchi H, Ohnuma H, Igarashi M, Kato T (2000) A novel mutation of the ceruloplasmin gene in a patient with heteroallelic ceruloplasmin gene mutation (HypoCPGM). Tohoku J Exp Med 191:119?125

3. Harris ZL, Durley AP, Man TK, Gitlin JD (1999) Targeted gene disruption reveals an essential role for ceruloplasmin in cellular iron efflux. Proc Natl Acad Sci U S A 96:10812?10817

4. Harris ZL, Takahashi Y, Miyajima H, Serizawa M, MacGillivray RT, Gitlin JD (1995) Aceruloplasminemia: molecular characterization of this disorder of iron metabolism. Proc Natl Acad Sci USA 92:2539?2543

5. Klomp LW, Farhangrazi ZS, Dugan LL, Gitlin JD (1996) Ceruloplasmin gene expression in the murine central nervous system. J Clin Invest 98:207?215

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