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Predominant ataxia, low ceruloplasmin, and absent K-F rings: Hypoceruloplasminemia or Wilson's disease
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| Published in: | Movement disorders 2010-10, Vol.25 (13), p.2260-2261 |
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| Main Authors: | , , , , , |
| Format: | Article |
| Language: | English |
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| cited_by | cdi_FETCH-LOGICAL-c3600-2577ce253cfbdd7db9b1e0e88695e9171f492477ac1a5422006bef3b3d3154dd3 |
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| cites | cdi_FETCH-LOGICAL-c3600-2577ce253cfbdd7db9b1e0e88695e9171f492477ac1a5422006bef3b3d3154dd3 |
| container_end_page | 2261 |
| container_issue | 13 |
| container_start_page | 2260 |
| container_title | Movement disorders |
| container_volume | 25 |
| creator | Mehta, Shyamal H. Parekh, Samir M. Prakash, Rajan Morgan, John C. Miyajima, Hiroaki Sethi, Kapil D. |
| description | |
| doi_str_mv | 10.1002/mds.23000 |
| format | article |
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| fulltext | fulltext |
| identifier | ISSN: 0885-3185 |
| ispartof | Movement disorders, 2010-10, Vol.25 (13), p.2260-2261 |
| issn | 0885-3185 1531-8257 |
| language | eng |
| recordid | cdi_crossref_primary_10_1002_mds_23000 |
| source | Wiley-Blackwell Read & Publish Collection |
| subjects | Adult Ataxia - physiopathology Basal Ganglia - metabolism Basal Ganglia - pathology Biological and medical sciences Ceruloplasmin - deficiency Ceruloplasmin - metabolism Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Female Hepatolenticular Degeneration - diagnosis Humans Iron Metabolism Disorders - diagnosis Magnetic Resonance Imaging - methods Medical sciences Neurodegenerative Diseases - diagnosis Neurology |
| title | Predominant ataxia, low ceruloplasmin, and absent K-F rings: Hypoceruloplasminemia or Wilson's disease |
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