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https://hdl.handle.net/2440/61395
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dc.contributor.author | Muller, K. | - |
dc.contributor.author | Padbury, R. | - |
dc.contributor.author | Jeffrey, G. | - |
dc.contributor.author | Poplawski, N. | - |
dc.contributor.author | Thompson, P. | - |
dc.contributor.author | Tonkin, A. | - |
dc.contributor.author | Harley, H. | - |
dc.date.issued | 2010 | - |
dc.identifier.citation | Liver Transplantation, 2010; 16(4):470-473 | - |
dc.identifier.issn | 1527-6465 | - |
dc.identifier.issn | 1527-6473 | - |
dc.identifier.uri | http://hdl.handle.net/2440/61395 | - |
dc.description.abstract | Transthyretin amyloid polyneuropathy, caused by mutations in the transthyretin gene, is a progressive condition for which liver transplantation is an established treatment. Favorable outcomes have been described in patients with the most common transthyretin mutation, Val30Met, but outcomes have been variable in patients with other mutations. We describe the cases of 2 siblings with transthyretin amyloid polyneuropathy secondary to an infrequently reported transthyretin mutation (Ala36Pro) who underwent liver transplantation with poor outcomes. | - |
dc.description.statementofresponsibility | Kate R. Muller, Robert Padbury, Gary P. Jeffrey, Nicola K. Poplawski, Philip Thompson, Anne Tonkin and Hugh A. J. Harley | - |
dc.language.iso | en | - |
dc.publisher | W B Saunders Co | - |
dc.rights | Copyright © 2010 American Association for the Study of Liver Diseases | - |
dc.source.uri | http://dx.doi.org/10.1002/lt.22019 | - |
dc.subject | Humans | - |
dc.subject | Amyloid Neuropathies, Familial | - |
dc.subject | Alanine | - |
dc.subject | Proline | - |
dc.subject | Prealbumin | - |
dc.subject | Treatment Outcome | - |
dc.subject | Liver Transplantation | - |
dc.subject | Fatal Outcome | - |
dc.subject | Genotype | - |
dc.subject | Mutation | - |
dc.subject | Adult | - |
dc.subject | Family Health | - |
dc.subject | Female | - |
dc.subject | Male | - |
dc.title | Poor outcome after liver transplantation for transthyretin amyloid neuropathy in a family with an Ala36Pro transthyretin mutation: Case report | - |
dc.type | Journal article | - |
dc.contributor.department | Medicine Learning and Teaching Unit | - |
dc.identifier.doi | 10.1002/lt.22019 | - |
pubs.publication-status | Published | - |
dc.identifier.orcid | Poplawski, N. [0000-0002-9372-3325] | - |
Appears in Collections: | Aurora harvest 5 Medicine publications |
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