| scholarly article | Q13442814 |
| P2093 | author name string | Takeo Kato | |
| Shinji Ohara | |||
| Kunimasa Arima | |||
| Kunihiro Yoshida | |||
| Kazuma Kaneko | |||
| Hiroaki Miyajima | |||
| Shu-ich Ikeda | |||
| Michiya Ohta | |||
| P2860 | cites work | Aceruloplasminemia: molecular characterization of this disorder of iron metabolism | Q24564471 |
| Chemistry and biochemistry of 4-hydroxynonenal, malonaldehyde and related aldehydes | Q28241500 | ||
| A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humans | Q28287958 | ||
| A case of hereditary ceruloplasmin deficiency with iron deposition in the brain associated with chorea, dementia, diabetes mellitus and retinal pigmentation: administration of fresh-frozen human plasma | Q30583066 | ||
| Glial fibrillary acidic protein is greatly modified by oxidative stress in aceruloplasminemia brain | Q31081111 | ||
| Alzheimer-type I astrogliopathy (AIA) and its implications for dynamic plasticity of astroglia: a historical review of the significance of AIA. | Q34197985 | ||
| Use of desferrioxamine in the treatment of aceruloplasminemia | Q34419336 | ||
| Familial apoceruloplasmin deficiency associated with blepharospasm and retinal degeneration | Q34690797 | ||
| Grumose or foamy spheroid bodies involving astrocytes in the human brain | Q34718835 | ||
| Hereditary caeruloplasmin deficiency: clinicopathological study of a patient | Q36834658 | ||
| Hereditary ceruloplasmin deficiency with hemosiderosis: a clinicopathological study of a Japanese family | Q42485956 | ||
| Glial fibrillary acidic protein immunohistochemical study of Alzheimer I & II astrogliosis in Wilson's disease | Q42510711 | ||
| Cerebellar ataxia associated with heteroallelic ceruloplasmin gene mutation | Q42514825 | ||
| Morphological investigations on axonal swellings and spheroids in various human diseases | Q48182756 | ||
| CSF abnormalities in patients with aceruloplasminemia | Q48370631 | ||
| An in vitro model for analysis of oxidative death in primary mouse astrocytes | Q48466995 | ||
| A novel splicing mutation in the ceruloplasmin gene responsible for hereditary ceruloplasmin deficiency with hemosiderosis | Q48484051 | ||
| A novel glycosylphosphatidylinositol-anchored form of ceruloplasmin is expressed by mammalian astrocytes | Q48638438 | ||
| P433 | issue | 12 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 1069-1077 | |
| P577 | publication date | 2002-12-01 | |
| P1433 | published in | Journal of Neuropathology & Experimental Neurology | Q15716771 |
| P1476 | title | Astrocytic deformity and globular structures are characteristic of the brains of patients with aceruloplasminemia | |
| P478 | volume | 61 |
| Q34218956 | 4-hydroxynonenal as a bioactive marker of pathophysiological processes |
| Q48446513 | A 70-year-old man with extrapyramidal symptoms, dementia and hemosiderosis |
| Q57255480 | Aceruloplasminemia |
| Q28830683 | Aceruloplasminemia With Psychomotor Excitement and Neurological Sign Was Improved by Minocycline (Case Report) |
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| Q60046955 | Aceruloplasminemia: Waiting for an Efficient Therapy |
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| Q54218847 | Ceruloplasmin gene-deficient mice with experimental autoimmune encephalomyelitis show attenuated early disease evolution. |
| Q35243074 | Ceruloplasmin protects against rotenone-induced oxidative stress and neurotoxicity |
| Q47355024 | Ceruloplasmin replacement therapy ameliorates neurological symptoms in a preclinical model of aceruloplasminemia. |
| Q48690775 | Coexistence of Copper in the Iron-Rich Particles of Aceruloplasminemia Brain |
| Q37808945 | Copper handling machinery of the brain |
| Q89927769 | Disorders of metal metabolism |
| Q37063770 | Hepcidin expression in mouse retina and its regulation via lipopolysaccharide/Toll-like receptor-4 pathway independent of Hfe. |
| Q28743561 | Identification and validation of novel cerebrospinal fluid biomarkers for staging early Alzheimer's disease |
| Q48591283 | Iron overload and antioxidative role of perivascular astrocytes in aceruloplasminemia |
| Q35032747 | Iron transport across the blood-brain barrier: development, neurovascular regulation and cerebral amyloid angiopathy |
| Q33616799 | Mechanisms of brain iron transport: insight into neurodegeneration and CNS disorders. |
| Q38161017 | The neuropathology of neurodegeneration with brain iron accumulation |
| Q36841623 | The pivotal role of astrocytes in the metabolism of iron in the brain. |
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