Aceruloplasminemia: neurodegeneration with brain iron accumulation (NBIA) associated with parkinsonism
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/s10545-014-9793-5
Reference4 articles.
1. Garcia-Cazorla A, Duarte ST (2014) Parkinsonism and inborn errors of metabolism. J Inherit Metab Dis 37:627–642
2. Kohno S, Miyajima H, Takahashi Y, Inoue Y (2000) Aceruloplasminemia with a novel mutation associated with parkinsonism. Neurogenetics 2:237–238
3. McNeill A, Pandolfo M, Kuhn J, Shang H, Miyajima H (2008) The neurological presentation of ceruloplasmin gene mutations. Eur Neurol 60:200–205
4. Miyajima H, Takahashi Y, Kono S (2003) Aceruloplasminemia, an inherited disorder of iron metabolism. Biometals 16:205–213
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2. Ceruloplasmin replacement therapy ameliorates neurological symptoms in a preclinical model of aceruloplasminemia;EMBO Molecular Medicine;2017-11-28
3. The Ferroxidase Hephaestin But Not Amyloid Precursor Protein is Required for Ferroportin-Supported Iron Efflux in Primary Hippocampal Neurons;Cellular and Molecular Neurobiology;2017-11-25
4. Neurodegeneration With Brain Iron Accumulation (NBIA);Diagnostic Imaging: Brain;2016
5. Neurodegeneration With Brain Iron Accumulation (NBIA);Imaging in Neurology;2016
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