A new transthyretin variant (Glu61Gly) associated with cardiomyopathy

By Rosenzweig Michael   Skinner Martha   Prokaeva Tatiana   Théberge Roger   Costello Catherine   Drachman Brian   Connors Lawreen  

Amyloid: The Journal of Protein Folding Disorders, Vol. 14, Iss. 1, 2007-01 ,pp. : 65-71

Informa Healthcare

Access to resources Recommend Favorite

A rare transthyretin mutation (Asp18Glu) associated with cardiomyopathy

By Connors Lawreen Heller   Yamashita Taro   Yazaki Masahide   Skinner Martha   Benson Merrill  

Amyloid: The Journal of Protein Folding Disorders, Vol. 11, Iss. 1, 2004-03 ,pp. : 61-66

Informa Healthcare

Access to resources Recommend Favorite

Familial amyloid polyneuropathy associated with the novel transthyretin variant Arg34Gly

By Levy Jaime  

Amyloid: The Journal of Protein Folding Disorders, Vol. 19, Iss. 4, 2012-12 ,pp. : 201-203

Informa Healthcare

Access to resources Recommend Favorite

Cardiomyopathy in a Japanese family with the Glu61Lys transthyretin variant: a new phenotype

By Noto Yuichi   Tokuda Takahiko   Shiga Kensuke   Tsuchiya Akiko   Yazaki Masahide   Matoba Satoaki   Nakagawa Masanori  

Amyloid: The Journal of Protein Folding Disorders, Vol. 16, Iss. 2, 2009-06 ,pp. : 99-102

Informa Healthcare

Access to resources Recommend Favorite

Technetium pyrophosphate myocardial uptake and peripheral neuropathy in a rare variant of familial transthyretin (TTR) amyloidosis (Ser23Asn): a case report and literature review

By Castaño Adam   Bokhari Sabahat   Brannagan Thomas H.   Wynn Julia   Maurer Mathew S.  

Amyloid: The Journal of Protein Folding Disorders, Vol. 19, Iss. 1, 2012-03 ,pp. : 41-46

Informa Healthcare

Access to resources Recommend Favorite