Petra Laššuthová Selected Research

Epilepsy (Aura)

1/2023	Neurodevelopmental and Epilepsy Phenotypes in Individuals With Missense Variants in the Voltage-Sensing and Pore Domains of KCNH5.
9/2021	Severe neurodevelopmental disorder with intractable seizures due to a novel SLC1A4 homozygous variant.

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Petra Laššuthová Research Topics

Disease

2	Epilepsy (Aura) 01/2023 - 09/2021
2	Infantile Epileptic-Dyskinetic Encephalopathy 10/2017 - 01/2017
1	Hereditary Sensory and Autonomic Neuropathies (HSAN) 12/2023
1	Brain Diseases (Brain Disorder) 11/2023
1	Infections 11/2023
1	Status Epilepticus (Complex Partial Status Epilepticus) 11/2023
1	Disease Progression 11/2023
1	Neurodevelopmental Disorders 01/2023
1	Birk-Barel Mental Retardation Dysmorphism Syndrome 01/2020
1	Intellectual Disability (Idiocy) 01/2019
1	Pelizaeus-Merzbacher Disease 07/2014

Drug/Important Bio-Agent (IBA)

2	Proteins (Proteins, Gene)FDA Link 01/2023 - 07/2014
2	Amino Acids FDA Link 09/2021 - 01/2020
1	Nerve Growth Factor (NGF)IBA 12/2023
1	ran-binding protein 2IBA 11/2023
1	DNA (Deoxyribonucleic Acid)IBA 11/2023
1	Voltage-Gated Potassium Channels (Voltage-Gated Potassium Channel)IBA 01/2023
1	Codon (Codons)IBA 09/2021
1	Anticonvulsants (Antiepileptic Drugs)IBA 01/2019
1	Cyclin-Dependent Kinases (cdk Proteins)IBA 10/2017
1	Chloral HydrateIBA 01/2017