Hereditary ceruloplasmin deficiency with hemosiderosis: a clinicopathological study of a Japanese family. - Test2 - elhamkhani - TriplyDB

Hereditary ceruloplasmin deficiency with hemosiderosis: a clinicopathological study of a Japanese family.

Hereditary ceruloplasmin deficiency with hemosiderosis: a clinicopathological study of a Japanese family.

http://www.wikidata.org/entity/Q42485956

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Neurodegeneration with brain iron accumulation: update on pathogenic mechanisms Animal models of age related macular degeneration Analysis of the human hephaestin gene and protein: comparative modelling of the N-terminus ecto-domain based upon ceruloplasmin Disruption of ceruloplasmin and hephaestin in mice causes retinal iron overload and retinal degeneration with features of age-related macular degeneration Brain and retinal ferroportin 1 dysregulation in polycythaemia mice Aceruloplasminemia With Psychomotor Excitement and Neurological Sign Was Improved by Minocycline (Case Report)Aceruloplasminemia: retinal histopathologic manifestations and iron-mediated melanosome degradation Identification of mineral deposits in the brain on radiological images: a systematic review.Impact of copper limitation on expression and function of multicopper oxidases (ferroxidases)Aceruloplasminemia.Iron in neurodegenerative disorders.Ceruloplasmin protects against rotenone-induced oxidative stress and neurotoxicity.Iron chelation therapy in aceruloplasminaemia: study of a patient with a novel missense mutation.Aceruloplasminaemia: a rare but important cause of iron overload.Targeted gene disruption reveals an essential role for ceruloplasmin in cellular iron efflux Copper Accumulates in Hemosiderins in Livers of Patients with Iron Overload Syndromes Impairment of interrelated iron- and copper homeostatic mechanisms in brain contributes to the pathogenesis of neurodegenerative disorders.The protective role of transferrin in Müller glial cells after iron-induced toxicity Review: Insights into molecular mechanisms of disease in neurodegeneration with brain iron accumulation: unifying theories.Hereditary caeruloplasmin deficiency: clinicopathological study of a patient.N-tert-butyl hydroxylamine, a mitochondrial antioxidant, protects human retinal pigment epithelial cells from iron overload: relevance to macular degeneration.The neuropsychiatry of hyperkinetic movement disorders: insights from neuroimaging into the neural circuit bases of dysfunction.Ceruloplasmin gene expression in the murine central nervous system.Gene expression profiling of mesenteric lymph nodes from sheep with natural scrapie.Molecular basis of iron-loading disorders.Review article: the iron overload syndromes.Cognitive impairment in "Other" movement disorders: hidden defects and valuable clues.Aceruloplasminemia presents as Type 1 diabetes in non-obese adults: a detailed case series.Treatment strategies in Alzheimer's disease: a review with focus on selenium supplementation.Impact of copper deficiency in humans.MRI findings in neuroferritinopathy.Mutual relationship between serum ferroxidase activity and hemoglobin levels in elderly individuals.Overexpressed or intraperitoneally injected human transferrin prevents photoreceptor degeneration in rd10 mice Astrocytic deformity and globular structures are characteristic of the brains of patients with aceruloplasminemia.Hereditary deficiency of ferroxidase (aka caeruloplasmin)Schizophrenia-like psychosis and aceruloplasminemia.Aceruloplasminemia: a novel mutation in a family with marked phenotypic variability.Ceruloplasmin replacement therapy ameliorates neurological symptoms in a preclinical model of aceruloplasminemia.Hereditary ferritinopathy: a novel mutation, its cellular pathology, and pathogenetic insights.Ceruloplasmin is Involved in the Nigral Iron Accumulation of 6-OHDA-Lesioned Rats.

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P2860

Hereditary ceruloplasmin deficiency with hemosiderosis: a clinicopathological study of a Japanese family.

http://www.wikidata.org/entity/Q42485956

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1995 nî lūn-bûn

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Hereditary ceruloplasmin defic ...... al study of a Japanese family.

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Annals of Neurology

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Ikeda S

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Kato M

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Morita H

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P2860

Hallervorden-Spatz syndrome and brain iron metabolism.

Iron metabolism in copper-deficient swine.

Familial apoceruloplasmin deficiency associated with blepharospasm and retinal degeneration.

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10.1002/ANA.410370515

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