Lena-Luise Becker

Charité - Universitätsmedizin Berlin

Germany

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Articles (17)

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2025

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2025

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2024

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2022

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2022

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2021

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2021

Collaborators (12)

Sebahattin Cirak

Professor for Neuropediatrics

Universität Ulm

GERMANY

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Konstantin L. Makridis

Charité - Universitätsmedizin Berlin

GERMANY

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Felix Boschann

GERMANY

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Darcy Krueger

Associate Professor

Cincinnati Children's Hospital Medical Center

UNITED STATES

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Victoria San Antonio‐Arce

GERMANY

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Angela M. Kaindl

GERMANY

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Georgia Ramantani

SWITZERLAND

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Joris Vriens

PI/ professor

KU Leuven

BELGIUM

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David Ritter

University of Cincinnati College of Medicine

UNITED STATES

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Astrid Bertsche

GERMANY

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Atef Mahmoud Mannaa

PRISM - Inserm Unit 1192 - Lille University

FRANCE

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Hormos Salimi Dafsari

GERMANY

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Lena-Luise Becker

Research Interests

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Articles (17)

Somatic DNA Variants in Epilepsy Surgery Brain Samples from Patients with Lesional Epilepsy

Phenotype Spectrum of TRPM3-Associated Disorders.

Mammalian Target of Rapamycin Inhibitor Levels Decrease Under Cenobamate Treatment

The importance of routine genetic testing in pediatric epilepsy surgery

The expanding clinical and genetic spectrum of DYNC1H1-related disorders.

Efficacy and safety of gene therapy with onasemnogene abeparvovec in children with spinal muscular atrophy in the D-A-CH-region: a population-based observational study

Epilepsy surgery in early infancy: A retrospective, multicenter study

Real‐world data on cannabidiol treatment of various epilepsy subtypes: A retrospective, multicenter study

Primidone improves symptoms in TRPM3‐linked developmental and epileptic encephalopathy with spike‐and‐wave activation in sleep

Corticosteroids in childhood epilepsies: A systematic review.

Proteome changes in autosomal recessive primary microcephaly.

Treatment of pediatric convulsive status epilepticus.

Beware of Neurotoxins in Common Plants: Water Hemlock Poisoning Presenting as Convulsive Status Epilepticus

Interferon receptor dysfunction in a child with malignant atrophic papulosis and CNS involvement.

Monoallelic CRMP1 gene variants cause neurodevelopmental disorder.

Genomic profiling in neuronal dyneinopathies and updated classifications

Lumbar Puncture Opening Pressure in Patients with Spinal Muscular Atrophy.

Collaborators (12)

Sebahattin Cirak

Konstantin L. Makridis

Felix Boschann

Darcy Krueger

Victoria San Antonio‐Arce

Angela M. Kaindl

Georgia Ramantani

Joris Vriens

David Ritter

Astrid Bertsche

Atef Mahmoud Mannaa

Hormos Salimi Dafsari

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