Hereditary cardiac amyloidosis associated with Pro24Ser transthyretin mutation: a case report
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1752-1947
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Hereditary cardiac amyloidosis associated with Pro24Ser transthyretin mutation: a case report ; volume:12 ; number:1 ; day:16 ; month:12 ; year:2018 ; pages:1-5 ; date:12.2018
Journal of medical case reports ; 12, Heft 1 (16.12.2018), 1-5, 12.2018
- Creator
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Yamamoto, Hiroyuki
Hashimoto, Toru
Kawamura, Shunji
Hiroe, Michiaki
Yamashita, Taro
Ando, Yukio
Yokochi, Tomoki
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s13256-018-1931-5
- URN
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urn:nbn:de:101:1-2019012821510494301711
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 11:02 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Yamamoto, Hiroyuki
- Hashimoto, Toru
- Kawamura, Shunji
- Hiroe, Michiaki
- Yamashita, Taro
- Ando, Yukio
- Yokochi, Tomoki
- SpringerLink (Online service)
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Sex differences in transthyretin cardiac amyloidosis
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Orthostatic hypotension in hereditary transthyretin amyloidosis: epidemiology, diagnosis and management
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Characterization of Transthyretin Mutation G47V Associated with Hereditary Cardiac Amyloidosis
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Hereditary transthyretin amyloidosis: a case report
Guideline of transthyretin-related hereditary amyloidosis for clinicians
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Sex differences in transthyretin cardiac amyloidosis
Becoming familiar with hereditary transthyretin amyloidosis, a treatable neuropathy
Conjunctival lymphangiectasia and retinal angiopathy in hereditary transthyretin amyloidosis
Orthostatic hypotension in hereditary transthyretin amyloidosis: epidemiology, diagnosis and management
Diagnosis and treatment of heart failure in hereditary transthyretin amyloidosis
A compound score to screen patients with hereditary transthyretin amyloidosis
Symptoms of Hereditary Transthyretin Amyloidosis: The Patient and Physician Perspective
Characterization of Transthyretin Mutation G47V Associated with Hereditary Cardiac Amyloidosis
Hereditary transthyretin amyloidosis overview
Hereditary transthyretin amyloidosis: a case report
Guideline of transthyretin-related hereditary amyloidosis for clinicians
Progressive brachial plexus enlargement in hereditary transthyretin amyloidosis
Sex differences in transthyretin cardiac amyloidosis
Becoming familiar with hereditary transthyretin amyloidosis, a treatable neuropathy
Conjunctival lymphangiectasia and retinal angiopathy in hereditary transthyretin amyloidosis
Orthostatic hypotension in hereditary transthyretin amyloidosis: epidemiology, diagnosis and management
Diagnosis and treatment of heart failure in hereditary transthyretin amyloidosis
A compound score to screen patients with hereditary transthyretin amyloidosis