C. P. J. Maury

Finnish hereditary amyloidosis is caused by a single nucleotide substitution in the gelsolin gene

C. P. J. Maury, Juha Kere, Riina Tolvanen et al. · FEBS Letters · 1990 · 137 citations

Finnish hereditary amyloidosis

C. P. J. Maury, K. Alii, Marc Baumann · FEBS Letters · 1990 · 118 citations · Full text

Amyloid and the origin of life: self-replicating catalytic amyloids as prebiotic informational and protometabolic entities

C. P. J. Maury · Cellular and Molecular Life Sciences · 2018 · 106 citations · Full text

Homozygosity for the Asn187 gelsolin mutation in Finnish-type familial amyloidosis is associated with severe renal disease

C. P. J. Maury, Juha Kere, Riina Tolvanen et al. · Genomics · 1992 · 64 citations

Urology, Medicine, Genetics +8

Isolation and characterization of cardiac amyloid in familial amyloid polyneuropathy type IV (Finnish): relation of the amyloid protein to variant gelsolin

C. P. J. Maury · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 1990 · 63 citations

Cardiomyopathy, Alzheimer's Disease, Amyloid Protein +4