Tarja Joensuu Selected Research

Megalencephaly

1/2018

Neonatal Alexander Disease: Novel GFAP Mutation and Comparison to Previously Published Cases.

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Tarja Joensuu Research Topics

Disease

7	Progressive Myoclonic Epilepsies (Progressive Myoclonic Epilepsy) 01/2021 - 02/2007
4	Neurodegenerative Diseases (Neurodegenerative Disease) 03/2015 - 02/2007
3	Seizures (Absence Seizure) 01/2018 - 01/2014
2	Unverricht-Lundborg Syndrome (Disease, Unverricht) 04/2015 - 05/2009
2	Ataxia (Dyssynergia) 03/2015 - 01/2014
2	Myoclonus (Nocturnal Myoclonus) 03/2015 - 01/2014
1	Brain Diseases (Brain Disorder) 01/2021
1	Muscle Hypotonia (Hypotonia) 01/2018
1	Benign Neonatal Epilepsy (Benign Familial Neonatal Convulsions) 01/2018
1	Megalencephaly 01/2018
1	PEHO syndrome 01/2017
1	Usher Syndromes (Usher Syndrome) 02/2007
1	Epilepsy (Aura) 02/2007

Drug/Important Bio-Agent (IBA)

7	Cystatin BIBA 01/2021 - 02/2007
2	Cysteine Proteases (Cysteine Protease)IBA 01/2021 - 01/2012
2	CathepsinsIBA 01/2021 - 02/2007
1	DolicholsIBA 01/2021
1	Pharmaceutical PreparationsIBA 01/2018
1	Codon (Codons)IBA 01/2017
1	Leucine (L-Leucine)FDA Link 01/2017
1	Proteins (Proteins, Gene)FDA Link 01/2017
1	Serine (L-Serine)FDA Link 01/2017
1	Mutant Proteins (Protein, Mutant)IBA 01/2017
1	OligonucleotidesIBA 02/2007
1	DNA (Deoxyribonucleic Acid)IBA 02/2007