NCL-taudit

name

• NCL-taudit

Works about NCL-taudit

• Animal model and molecular interactions of Cln5
• CLN5 - from mutation to defective protein and clinical phenotype
• Dissection of the genetic background of childhood onset progressive myoclonic epilepsies
• Electrophysiology of visual pathways as a screening tool for neurodegenerative diseases :
• INCL-kansio
• Juvenile neuronal ceroid lipofuscinosis : brain-related symptoms and their treatment
• Juvenile neuronal ceroid lipofuscinosis : psychiatric symptoms, GAD-autoantibodies and response to medication
• Molecular and cell biology of infantile (CLN1) and variant late infantile (CLN5) neuronal ceroid lipofuscinoses
• Molecular and cellular mechanisms behind juvenile neuronal ceroid lipofuscinosis (JNCL, Batten disease)
• Molecular interactions of neuronal ceroid lipofuscinosis protein CLN3
• Molecular interactions underlying neuronal ceroid lipofuscinoses CLN1 and CLN5
• Mustat pallot : kertomuksia lapsen sairaudesta
• Neurodevelopmental insights into rare diseases :
• Neuromagnetic studies on somatosensory functions in CLN3, CLN5 and CLN8 forms of neuronal ceroid lipofuscinoses
• Stem cells in neurodegenerative diseases :
• Struktuuria opetukseen : selkeys ja rakenteet oppimisen edistäjänä
• Studies on palmitoyl-protein thioesterase 1 : implications for synaptic functions
• Studies on the molecular pathogenesis of neuronal ceroid lipofuscinoses in the animal models of CLN8 and CLN10
• The CLN5 disease : protein maturation, trafficking and pathology
• Unravelling molecular and cellular disease mechanisms in infantile neuronal ceroid lipofuscinosis (INCL)