TY  -  
T1  - Juvenile neuronal ceroid lipofuscinosis; psychiatric symptoms, GAD-autoantibodies, and response to medication 
SN  -  /  
UR  - URN:ISBN:978-952-92-5118-6; http://hdl.handle.net/10138/22535 
T3  -  
A1  - Talling, Maria Louise 
A2  -  
PB  -  
Y1  - 2009 
LA  - eng 
AB  - Juvenile neuronal ceroid lipofuscinosis (JNCL) is one of the most common neurodegenerative diseases in childhood. Its clinical onset, with visual failure as the first sign, is between the ages of 4 to 8 years. During the disease progress, epilepsy, motor symptoms, cognitive decline, and psychiatric symptoms become apparent. It leads to premature death between ages 15 and 30. Treatment consists of symptomatic drug administration and various forms of rehabilitation, but to date, no curative treatm... 
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KW  - lastenneurologia 
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