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Moritz Tacke Selected Research

Atrophy

12/2018SACS variants are a relevant cause of autosomal recessive hereditary motor and sensory neuropathy.

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Moritz Tacke Research Topics

Disease

4Rolandic Epilepsy (Centrotemporal Epilepsy)
03/2021 - 11/2016
3Epilepsy (Aura)
12/2020 - 05/2018
2Stroke (Strokes)
06/2020 - 01/2018
1Generalized Epilepsy
12/2020
1Partial Epilepsies (Epilepsy, Partial)
12/2020
1Fatigue
10/2020
1Atrophy
12/2018
1Peripheral Nervous System Diseases (PNS Diseases)
12/2018
1Spastic ataxia Charlevoix-Saguenay type
12/2018
1Cerebellar Ataxia (Dysmetria)
12/2018
1Tuberous Sclerosis (Bourneville's Disease)
05/2018

Drug/Important Bio-Agent (IBA)

4Levetiracetam (Keppra)FDA LinkGeneric
03/2021 - 11/2016
4sulthiame (sultiam)IBA
03/2021 - 11/2016
3Anticonvulsants (Antiepileptic Drugs)IBA
03/2021 - 11/2016
1Clobazam (HR 376)IBA
03/2021
1Immunoglobulin E (IgE)IBA
12/2020
1SteroidsIBA
10/2020
1atalurenIBA
10/2020
1Vitamin B 6IBA
02/2019
1Retinaldehyde (Retinal)IBA
12/2018
1trans-sodium crocetinate (crocetin)IBA
05/2018
1Indicators and Reagents (Reagents)IBA
01/2018

Therapy/Procedure

3Therapeutics
10/2020 - 11/2016
1Drug Therapy (Chemotherapy)
03/2021
1Thrombectomy
06/2020