Henry Hing Cheong Lee

11PUBLICATIONS
39CO-AUTHORS
Neurology and neuromuscular diseasesElectrochemical energy storage and conversionGene expression (incl. microarray and other genome-wide approaches)Molecular targetsPeople with disability
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Publications (11)

|Sep 30, 2026
Kv3.1 activation suppresses provoked and spontaneous seizures in a mouse Dravet syndrome model.

|Apr 03, 2026
Postnatal gene restoration in succinic semialdehyde dehydrogenase deficiency (SSADHD) reveals phenotype reversibility.

Henry H C Lee, Gabrielle McGinty, Amanda Liebhardt

|Jul 31, 2025
Central Dysmyelination in SSADH-Deficient Humans and Mice.

Itay Tokatly Latzer, Henry H C Lee, Edward Yang

|Feb 14, 2025
Phenotypic rescue via mTOR inhibition in neuron-specific Pten knockout mice reveals AKT and mTORC1-site specific changes.

Angelica D'Amore, Maria Sundberg, Rui Lin

|Apr 24, 2024
Clinical and molecular outcomes from the 5-Year natural history study of SSADH Deficiency, a model metabolic neurodevelopmental disorder.

Itay Tokatly Latzer, Jean-Baptiste Roullet, Wardiya Afshar-Saber

|Apr 06, 2024
Gene replacement therapies for inherited disorders of neurotransmission: Current progress in succinic semialdehyde dehydrogenase deficiency.

Henry H C Lee, Itay Tokatly Latzer, Mariarita Bertoldi

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Frequent Collaborators

8 joint publications

Phillip L Pearl

8 joint publications

Alexander Rotenberg

5 joint publications

Mustafa Sahin

5 joint publications

Itay Tokatly Latzer