{"_buckets": {"deposit": "b593b64e-4051-40ae-892e-856cdc14ce52"}, "_deposit": {"id": "25053", "owners": [], "pid": {"revision_id": 0, "type": "depid", "value": "25053"}, "status": "published"}, "_oai": {"id": "oai:nagoya.repo.nii.ac.jp:00025053"}, "item_10_biblio_info_6": {"attribute_name": "\u66f8\u8a8c\u60c5\u5831", "attribute_value_mlt": [{"bibliographicIssueDates": {"bibliographicIssueDate": "2017-11", "bibliographicIssueDateType": "Issued"}, "bibliographicIssueNumber": "11", "bibliographicPageEnd": "907", "bibliographicPageStart": "901", "bibliographicVolumeNumber": "88", "bibliographic_titles": [{"bibliographic_title": "JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY"}]}]}, "item_10_description_4": {"attribute_name": "\u6284\u9332", "attribute_value_mlt": [{"subitem_description": "Purpose Amyotrophic lateral sclerosis (ALS) presents with varying degrees of brain degeneration that can extend beyond the corticospinal tract (CST). Furthermore, the clinical course and progression of ALS varies widely. Brain degeneration detected using structural MRI could reflect disease progression.\n\\nSubjects and methods On study registration, 3-Tesla volumetric MRI and diffusion tensor imaging scans were obtained at baseline in 38 healthy controls and 67 patients with sporadic ALS. Patients had Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised (ALSFRS-R) scores of \u226536\u2009and did not have the chromosome 9, open reading frame 72 repeat expansion. Six months later, changes in ALSFRS-R (\u0394ALSFRS-R) scores were calculated and patients were grouped into three categories, namely, patients with slow progression with \u0394ALSFRS-R scores \u22643 (n=19), intermediate progression with \u0394ALSFRS-R scores =4, 5 and 6 (n=36) and rapid progression with \u0394ALSFRS-R scores \u22657 (n=12). We analysed voxel-based morphometry and tract-based spatial statistics among these subgroups and controls.\n\\nResults In comparison with controls, patients with ALS showed grey matter atrophy and decreased fractional anisotropy beyond the motor cortex and CST, especially in the frontotemporal lobes and basal ganglia. Moreover, the degree of change was highly proportional to \u0394ALSFRS-R at the 6-month assessment.\n\\nConclusion A more rapid disease progression and poorer functional decline were associated with greater involvement of the extra-motor cortex and basal ganglia, suggesting that the spatial extent of brain involvement can be an indicator of the progression in ALS.", "subitem_description_type": "Abstract"}]}, "item_10_identifier_60": {"attribute_name": "URI", "attribute_value_mlt": [{"subitem_identifier_type": "DOI", "subitem_identifier_uri": "http://doi.org/10.1136/jnnp-2016-314337"}, {"subitem_identifier_type": "HDL", "subitem_identifier_uri": "http://hdl.handle.net/2237/27262"}]}, "item_10_publisher_32": {"attribute_name": "\u51fa\u7248\u8005", "attribute_value_mlt": [{"subitem_publisher": "BMJ Publishing"}]}, "item_10_rights_12": {"attribute_name": "\u6a29\u5229", "attribute_value_mlt": [{"subitem_rights": "Copyright 2017 BMJ Publishing . The following article appeared in (JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. v.88, n.11, 2017, p.901-907) and may be found at (http://dx.doi.org/10.1136/jnnp-2016-314337)."}]}, "item_10_select_15": {"attribute_name": "\u8457\u8005\u7248\u30d5\u30e9\u30b0", "attribute_value_mlt": [{"subitem_select_item": "author"}]}, "item_10_source_id_7": {"attribute_name": "ISSN", "attribute_value_mlt": [{"subitem_source_identifier": "0022-3050", "subitem_source_identifier_type": "ISSN"}]}, "item_creator": {"attribute_name": "\u8457\u8005", "attribute_type": "creator", "attribute_value_mlt": [{"creatorNames": [{"creatorName": "Senda, Joe"}], "nameIdentifiers": [{"nameIdentifier": "74713", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Atsuta, Naoki"}], "nameIdentifiers": [{"nameIdentifier": "74714", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Watanabe, Hirohisa"}], "nameIdentifiers": [{"nameIdentifier": "74715", "nameIdentifierScheme": 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