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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2005 | 1 |
2012 | 1 |
2013 | 1 |
2015 | 1 |
2017 | 1 |
2018 | 1 |
2024 | 0 |
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Cardiomyopathy in Swedish patients with the Gly53Glu and His88Arg transthyretin variants.
Amyloid. 2005 Sep;12(3):184-8. doi: 10.1080/13506120500223126.
Amyloid. 2005.
PMID: 16194874
Disease profile and differential diagnosis of hereditary transthyretin-related amyloidosis with exclusively cardiac phenotype: an Italian perspective.
Rapezzi C, Quarta CC, Obici L, Perfetto F, Longhi S, Salvi F, Biagini E, Lorenzini M, Grigioni F, Leone O, Cappelli F, Palladini G, Rimessi P, Ferlini A, Arpesella G, Pinna AD, Merlini G, Perlini S.
Rapezzi C, et al.
Eur Heart J. 2013 Feb;34(7):520-8. doi: 10.1093/eurheartj/ehs123. Epub 2012 Jun 28.
Eur Heart J. 2013.
PMID: 22745357
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A genealogical and clinical study of the phenotypical variation within the Swedish transthyretin His88Arg (p. His108Arg) amyloidosis family.
Hellman U, Lundgren HE, Westermark P, Stafberg C, Nahi H, Tachlinski S, Guggi M, Flogegård M, Hamid M, Escher SA, Suhr OB.
Hellman U, et al.
Eur J Med Genet. 2015 Apr;58(4):211-5. doi: 10.1016/j.ejmg.2015.02.005. Epub 2015 Feb 24.
Eur J Med Genet. 2015.
PMID: 25721874
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Coronary ectasia in amyloid cardiomyopathy and neuropathy due to the transthyretin mutation c.323A>G.
Finsterer J, Stöllberger C, Rauschka H, Gatterer E.
Finsterer J, et al.
Heart Lung. 2018 Mar-Apr;47(2):127-129. doi: 10.1016/j.hrtlng.2017.11.007. Epub 2017 Dec 13.
Heart Lung. 2018.
PMID: 29246775
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