Differentiation of light chain cardiac amyloidosis and hypertrophic cardiomyopathy by ensemble machine learning-based radiomic analysis of cardiac magnetic resonance.
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| Title: | Differentiation of light chain cardiac amyloidosis and hypertrophic cardiomyopathy by ensemble machine learning-based radiomic analysis of cardiac magnetic resonance. |
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| Authors: | Zhang, Shuyuan1 (AUTHOR), Guo, Yubo2 (AUTHOR), Gao, Yuze3 (AUTHOR), Wu, Ming1 (AUTHOR), Zhuang, Shengsheng1 (AUTHOR), Li, Xiao2 (AUTHOR), Chen, Ting3 (AUTHOR), Li, Jian4 (AUTHOR), Tian, Zhuang1 (AUTHOR) tianzhuangcn@sina.com, Wang, Yining2 (AUTHOR) wangyining@pumch.cn, Zhang, Shuyang1 (AUTHOR) shuyangzhang103@nrdrs.org |
| Source: | Orphanet Journal of Rare Diseases. 11/4/2025, Vol. 20 Issue 1, p1-11. 11p. |
| Database: | Academic Search Ultimate |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 189086676 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Differentiation of light chain cardiac amyloidosis and hypertrophic cardiomyopathy by ensemble machine learning-based radiomic analysis of cardiac magnetic resonance. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Zhang%2C+Shuyuan%22">Zhang, Shuyuan</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Guo%2C+Yubo%22">Guo, Yubo</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Gao%2C+Yuze%22">Gao, Yuze</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Wu%2C+Ming%22">Wu, Ming</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Zhuang%2C+Shengsheng%22">Zhuang, Shengsheng</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Li%2C+Xiao%22">Li, Xiao</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Chen%2C+Ting%22">Chen, Ting</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Li%2C+Jian%22">Li, Jian</searchLink><relatesTo>4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Tian%2C+Zhuang%22">Tian, Zhuang</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> tianzhuangcn@sina.com</i><br /><searchLink fieldCode="AR" term="%22Wang%2C+Yining%22">Wang, Yining</searchLink><relatesTo>2</relatesTo> (AUTHOR)<i> wangyining@pumch.cn</i><br /><searchLink fieldCode="AR" term="%22Zhang%2C+Shuyang%22">Zhang, Shuyang</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> shuyangzhang103@nrdrs.org</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Orphanet+Journal+of+Rare+Diseases%22">Orphanet Journal of Rare Diseases</searchLink>. 11/4/2025, Vol. 20 Issue 1, p1-11. 11p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=189086676 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s13023-025-03947-2 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 11 StartPage: 1 Titles: – TitleFull: Differentiation of light chain cardiac amyloidosis and hypertrophic cardiomyopathy by ensemble machine learning-based radiomic analysis of cardiac magnetic resonance. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Zhang, Shuyuan – PersonEntity: Name: NameFull: Guo, Yubo – PersonEntity: Name: NameFull: Gao, Yuze – PersonEntity: Name: NameFull: Wu, Ming – PersonEntity: Name: NameFull: Zhuang, Shengsheng – PersonEntity: Name: NameFull: Li, Xiao – PersonEntity: Name: NameFull: Chen, Ting – PersonEntity: Name: NameFull: Li, Jian – PersonEntity: Name: NameFull: Tian, Zhuang – PersonEntity: Name: NameFull: Wang, Yining – PersonEntity: Name: NameFull: Zhang, Shuyang IsPartOfRelationships: – BibEntity: Dates: – D: 04 M: 11 Text: 11/4/2025 Type: published Y: 2025 Identifiers: – Type: issn-print Value: 17501172 Numbering: – Type: volume Value: 20 – Type: issue Value: 1 Titles: – TitleFull: Orphanet Journal of Rare Diseases Type: main |
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