Hereditary gelsolin amyloidosis

Author:

Kiuru-Enari Sari,Haltia Matti

Publisher

Elsevier

Reference133 articles.

1. Lattice corneal dystrophy type II associated with familial amyloidosis, Finnish type (FAF);Akiya;Ophthalmology,1996

2. Investigation of AGE, their receptor and NF-kB activation and apoptosis in patients with ATTR and Gelsolin amyloidosis;Anan;Histol Histopathol,2010

3. Cytoplasmic gelsolin increases mitochondrial activity and reduces Aβ burden in a mouse model of Alzheimer’s disease;Antequera;Neurobiol Dis,2009

4. Amyloidosis-related nephrotic syndrome due to a G654A gelsolin mutation: the first report from the Middle East;Ardalan;Nephrol Dial Transplant,2007

5. Hereditary gelsolin amyloidosis in Iran: the first report from the Middle East;Ardalan,2007

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