Amyloidosis
This volume presents a comprehensive overview of amyloidosis, beginning with a general historical overview and proceeding to a discussion of the subtypes of amyloidosis encountered in clinical medicine. The unifying feature common to all amyloidoses, that of misfolded proteins, is explored in some d...
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| Formato: | Online |
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| Lenguaje: | inglés |
| Publicado: |
IntechOpen
2022
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| Materias: | |
| Acceso en línea: | ONIX_20220727_9781839692987_70 |
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| _version_ | 1869518565748506624 |
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| collection | Directory of Open Access Books |
| description | This volume presents a comprehensive overview of amyloidosis, beginning with a general historical overview and proceeding to a discussion of the subtypes of amyloidosis encountered in clinical medicine. The unifying feature common to all amyloidoses, that of misfolded proteins, is explored in some detail, and the pathobiology and manifestations are delineated for major disease entities. Both inherited and acquired amyloidosis are examined, and a discussion of current treatment approaches are included for many of these subsets. It is hoped that the volume will be useful to readers who approach the topic from a wide variety of disciplines. |
| format | Online |
| id | doab-20.500.12854ir-90174 |
| institution | Directory of Open Access Books |
| language | eng |
| publishDate | 2022 |
| publishDateRange | 2022 |
| publishDateSort | 2022 |
| publisher | IntechOpen |
| publisherStr | IntechOpen |
| record_format | ojs |
| spelling | doab-20.500.12854ir-901742024-03-31T22:45:33Z Amyloidosis Harrison, Jonathan S. Medical diagnosis thema EDItEUR::M Medicine and Nursing::MJ Clinical and internal medicine::MJA Medical diagnosis This volume presents a comprehensive overview of amyloidosis, beginning with a general historical overview and proceeding to a discussion of the subtypes of amyloidosis encountered in clinical medicine. The unifying feature common to all amyloidoses, that of misfolded proteins, is explored in some detail, and the pathobiology and manifestations are delineated for major disease entities. Both inherited and acquired amyloidosis are examined, and a discussion of current treatment approaches are included for many of these subsets. It is hoped that the volume will be useful to readers who approach the topic from a wide variety of disciplines. 2022-07-27T08:14:18Z 2022-07-27T08:14:18Z 2022 book ONIX_20220727_9781839692987_70 9781839692987 9781839692970 9781839692994 https://directory.doabooks.org/handle/20.500.12854/90174 eng image/jpeg n/a https://www.intechopen.com/books/9046 https://mts.intechopen.com/storage/books/9046/authors_book/authors_book.pdf IntechOpen IntechOpen 10.5772/intechopen.83041 10.5772/intechopen.83041 78a36484-2c0c-47cb-ad67-2b9f5cd4a8f6 9781839692987 9781839692970 9781839692994 IntechOpen 118 open access |
| spellingShingle | Medical diagnosis thema EDItEUR::M Medicine and Nursing::MJ Clinical and internal medicine::MJA Medical diagnosis Amyloidosis |
| title | Amyloidosis |
| title_full | Amyloidosis |
| title_fullStr | Amyloidosis |
| title_full_unstemmed | Amyloidosis |
| title_short | Amyloidosis |
| title_sort | amyloidosis |
| topic | Medical diagnosis thema EDItEUR::M Medicine and Nursing::MJ Clinical and internal medicine::MJA Medical diagnosis |
| topic_facet | Medical diagnosis thema EDItEUR::M Medicine and Nursing::MJ Clinical and internal medicine::MJA Medical diagnosis |
| url | ONIX_20220727_9781839692987_70 |