Vitreous amyloidosis in familial amyloidotic polyneuropathy. Report of a case with the Val30Met transthyretin mutation
- 31 December 1995
- journal article
- review article
- Published by Elsevier in Survey of Ophthalmology
- Vol. 40 (3) , 197-206
- https://doi.org/10.1016/s0039-6257(95)80026-3
Abstract
No abstract availableKeywords
This publication has 90 references indexed in Scilit:
- Variant apolipoprotein AI as a major constituent of a human hereditary amyloidBiochemical and Biophysical Research Communications, 1988
- Hereditary Cerebral Amyloid Angiopathy: The amyloid fibrils contain a protein which is a variant of Cystatin C, an inhibitor of lysosomal cysteine proteasesBiochemical and Biophysical Research Communications, 1986
- A new form of amyloid protein associated with chronic hemodialysis was identified as β2-microglobulinBiochemical and Biophysical Research Communications, 1985
- A variant prealbumin-related low molecular weight amyloid fibril protein in familial amyloid polyneuropathy of Japanese originBiochemical and Biophysical Research Communications, 1984
- Identification of a prealbumin variant in the serum of a Japanese patient with familial amyloidotic polyneuropathyBiochemical and Biophysical Research Communications, 1984
- Identification of amyloid prealbumin variant in familial amyloidotic polyneuropathy (Japanese type)Biochemical and Biophysical Research Communications, 1983
- Polymorphism of human plasma thyroxine binding prealbuminBiochemical and Biophysical Research Communications, 1983
- Amyloid Deposits and AmyloidosisNew England Journal of Medicine, 1980
- Amyloid Deposits and AmyloidosisNew England Journal of Medicine, 1980
- Primary familial amyloidosis with vitreous opacitiesActa Neuropathologica, 1978