Amyloid fibrils containing fragmented ATTR may be the standard fibril composition in ATTR amyloidosis

Long-term data from the Familial Amyloidotic Polyneuropathy World Transplant Registry (FAPWTR)

(2011) H. E. Wilczek et al.   AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS

A possible role for miRNA silencing in disease phenotype variation in Swedish transthyretin V30M carriers

(2010) Malin Olsson et al.   BMC Medical Genetics

Variation in amount of wild-type transthyretin in different fibril and tissue types in ATTR amyloidosis

(2010) Elisabet Ihse et al.   JOURNAL OF MOLECULAR MEDICINE-JMM

Mitochondrial haplogroup is associated with the phenotype of familial amyloidosis with polyneuropathy in Swedish and French patients

(2009) M Olsson et al.   CLINICAL GENETICS

Distinct characteristics of amyloid deposits in early- and late-onset transthyretin Val30Met familial amyloid polyneuropathy

(2009) Haruki Koike et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Complement C1Q polymorphisms modulate onset in familial amyloidotic polyneuropathy TTR Val30Met

(2009) Efthimios Dardiotis et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Clinical symptomatic de novo systemic transthyretin amyloidosis 9 years after domino liver transplantation

(2009) Ana Paula Barreiros et al.   LIVER TRANSPLANTATION

Amyloid fibril composition is related to the phenotype of hereditary transthyretin V30M amyloidosis

(2008) E Ihse et al.   JOURNAL OF PATHOLOGY