| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1159/000008091 |
| P8608 | Fatcat ID | release_opc23qz4szar7nyfzvetwei4we |
| P698 | PubMed publication ID | 10529542 |
| P2093 | author name string | Okabe T | |
| Ohta M | |||
| Yonekawa M | |||
| Asamoto Y | |||
| P433 | issue | 3 | |
| P921 | main subject | Huntington's disease | Q190564 |
| P304 | page(s) | 157-162 | |
| P577 | publication date | 1999-01-01 | |
| P1433 | published in | European Neurology | Q1376833 |
| P1476 | title | 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 | |
| P478 | volume | 42 |
| Q48362634 | Aceruloplasminaemia: a disorder of diabetes and neurodegeneration |
| Q35614916 | Aceruloplasminaemia: a rare but important cause of iron overload |
| Q64071900 | Aceruloplasminemia: A Severe Neurodegenerative Disorder Deserving an Early Diagnosis |
| Q60046955 | Aceruloplasminemia: Waiting for an Efficient Therapy |
| Q81073475 | Aceruloplasminemia: a case report |
| Q42528707 | Astrocytic deformity and globular structures are characteristic of the brains of patients with aceruloplasminemia |
| Q47355024 | Ceruloplasmin replacement therapy ameliorates neurological symptoms in a preclinical model of aceruloplasminemia. |
| Q42795465 | Clinical and imaging characteristics of late onset mitochondrial membrane protein-associated neurodegeneration (MPAN) |
| Q48690775 | Coexistence of Copper in the Iron-Rich Particles of Aceruloplasminemia Brain |
| Q31104114 | Decreased T2 signal in the thalami may be a sign of lysosomal storage disease |
| Q37928941 | Disorders associated with systemic or local iron overload: from pathophysiology to clinical practice |
| Q48559379 | Genomic responses of the brain to ischemic stroke, intracerebral haemorrhage, kainate seizures, hypoglycemia, and hypoxia |
| Q34329790 | Hepatic but not brain iron is rapidly chelated by deferasirox in aceruloplasminemia due to a novel gene mutation |
| Q38826931 | Hereditary chorea - what else to consider when the Huntington's disease genetics test is negative? |
| Q35596505 | Iron chelation therapy in aceruloplasminaemia: study of a patient with a novel missense mutation. |
| Q48591283 | Iron overload and antioxidative role of perivascular astrocytes in aceruloplasminemia |
| Q34365355 | Iron overload, oxidative stress, and axonal dystrophy in brain disorders |
| Q48438596 | Is aceruloplasminemia treatable? Combining iron chelation and fresh-frozen plasma treatment. |
| Q28262783 | Risk factors for dementia |
| Q64043172 | [Aceruloplasminemia : Diagnosis and treatment of a rare disease] |
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