TY  -  
T1  - Natural course of Finnish gelsolin amyloidosis 
SN  -  /  
UR  - URN:NBN:fi:hulib-201512164049; http://hdl.handle.net/10138/159500 
T3  -  
A1  - Nikoskinen, Tuuli; Schmidt, Eeva-Kaisa; Strbian, Daniel; Kiuru-Enari, Sari; Atula, Sari 
A2  -  
PB  - Helsingfors universitet 
Y1  - 2015 
LA  - eng 
AB  - Background: Finnish type of hereditary gelsolin amyloidosis (FGA) is one of the most common diseases of Finnish disease heritage. Existing FGA knowledge is based only on smaller patient series, so our aim was to elucidate the natural course of the disease in a comprehensive sample of patients and to build up a national FGA patient registry.

Methods: An inquiry about the known and suspected signs of FGA, sent to the members of Finnish Amyloidosis Association, telephone contacts and hospital re... 
VO  -  
IS  -  
SP  -  
OP  -  
KW  - amyloidosis; course; disease progression; familial; Finnish type amyloidosis; gelsolin-related amyloidosis; Meretoja syndrome; Neurology; Neurologia; Neurologi 
N1  -   
PP  -  
ER  -