Clinical and Molecular Genetic Characterization of Landau Kleffner Syndrome: An Observational Cohort and Experimental Study

For LKS, early intervention is important for long-term outcomes. Furthermore, management should not be based solely on electroencephalogram findings. Genetic and functional investigations offer insights into disease pathophysiology and facilitate development of future targeted therapies. ANN NEUROL 2025;98:951-966.

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Publication Details

Journal
Annals of Neurology
Published
2025-09-13
DOI
https://doi.org/10.1002/ana.27306
Citations
1
Primary Topic
Genetics and Neurodevelopmental Disorders
Type
article
Field-Weighted Citation Impact
1.82

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article

Clinical and Molecular Genetic Characterization of Landau Kleffner Syndrome: An Observational Cohort and Experimental Study

Judith Helen Cross, Sean D. Fraser, Manju A. Kurian, Rebecca Greenaway et al.
1 citations
Annals of Neurology
Genetics and Neurodevelopmental Disorders
1.82
article

Clinical and Molecular Genetic Characterization of Landau Kleffner Syndrome: An Observational Cohort and Experimental Study

Judith Helen Cross, Sean D. Fraser, Manju A. Kurian, Rebecca Greenaway, Lachlan De Hayr, Maria Clark, Joseph W. Lynch, Victoria L. Harvey, Dimitri M. Kullmann, Dale Moulding, Kimberley M. Reid, Adeline Ngoh, Xiumin Chen, Katy Barwick, Natalie Trump, Esther Meyer
article en
1 citations

Abstract

For LKS, early intervention is important for long-term outcomes. Furthermore, management should not be based solely on electroencephalogram findings. Genetic and functional investigations offer insights into disease pathophysiology and facilitate development of future targeted therapies. ANN NEUROL 2025;98:951-966.

Annals of NeurologyVol. 98(5)
The University of Queensland (AU), University of the Sunshine Coast (AU), Great Ormond Street Hospital (GB), Sunshine Coast University Hospital (AU), KK Women's and Children's Hospital (SG), National Hospital for Neurology and Neurosurgery (GB), University College London (GB)
Wellcome Trust, Action Medical Research, National Institute for Health and Care Research, Guarantors of Brain, Rosetrees Trust, Great Ormond Street Hospital Charity, Medical Research Council, National Health and Medical Research Council
Openalex Percentile: Top 13%
Genetics and Neurodevelopmental Disorders
1.82
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