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Imane Abdelmoumen Selected Research

5,10-methenyltetrahydrofolate synthetase

12/2019A case of 5,10-methenyltetrahydrofolate synthetase deficiency due to biallelic null mutations with novel findings of elevated neopterin and macrocytic anemia.

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Imane Abdelmoumen Research Topics

Disease

2Drug Resistant Epilepsy
01/2021 - 02/2014
1Dyskinesias (Dyskinesia)
01/2021
1Microcephaly
12/2019
1Macrocytic Anemia
12/2019
1Epilepsy (Aura)
12/2019
1Status Epilepticus (Complex Partial Status Epilepticus)
05/2012

Drug/Important Bio-Agent (IBA)

1AMPA Receptors (AMPA Receptor)IBA
01/2021
15,10-methenyltetrahydrofolate synthetaseIBA
12/2019
1NeopterinIBA
12/2019
1Diazepam (Valium)FDA LinkGeneric
05/2012

Therapy/Procedure

1Vagus Nerve Stimulation
02/2014