HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Tarja Joensuu Selected Research

Progressive Myoclonic Epilepsies (Progressive Myoclonic Epilepsy)

1/2021Progressive myoclonus epilepsies-Residual unsolved cases have marked genetic heterogeneity including dolichol-dependent protein glycosylation pathway genes.
4/2015Refining the phenotype of Unverricht-Lundborg disease (EPM1): a population-wide Finnish study.
3/2015Abnormal microglial activation in the Cstb(-/-) mouse, a model for progressive myoclonus epilepsy, EPM1.
1/2014Gene expression alterations in the cerebellum and granule neurons of Cstb(-/-) mouse are associated with early synaptic changes and inflammation.
1/2012Early microglial activation precedes neuronal loss in the brain of the Cstb-/- mouse model of progressive myoclonus epilepsy, EPM1.
5/2009Cystatin B deficiency sensitizes neurons to oxidative stress in progressive myoclonus epilepsy, EPM1.
2/2007Cystatin B: mutation detection, alternative splicing and expression in progressive myclonus epilepsy of Unverricht-Lundborg type (EPM1) patients.

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown:


Tarja Joensuu Research Topics

Disease

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

Drug/Important Bio-Agent (IBA)

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