Henry Hing Cheong Lee (Henry H C Lee)

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 21

Top Topics

Severe Traumatic Brain Injury

Replacement Therapy

Subarachnoid Hemorrhage

Top Venues

Journal of inherited metabolic disease

Journal of neurodevelopmental disorders

Journal of sleep research

Cerebral cortex (New York, N.Y. : 1991)

This page only lists publications with an associated author ORCID identifier.

Publications

Henry Hing Cheong Lee, Itay Tokatly Latzer, Mariarita Bertoldi, Guangping Gao, Phillip L Pearl, Mustafa Sahin, Alexander Rotenberg
Gene replacement therapies for inherited disorders of neurotransmission: Current progress in succinic semialdehyde dehydrogenase deficiency. Journal of inherited metabolic disease 47 (3) (2024)
Itay Tokatly Latzer, Jean-Baptiste Roullet, Wardiya Afshar Saber, Henry Hing Cheong Lee, Mariarita Bertoldi, Gabrielle E McGinty, Melissa L DiBacco, Erland Arning, Melissa Tsuboyama, Alexander Rotenberg, Thomas Opladen, Kathrin Jeltsch, Àngels García-Cazorla, Natalia Juliá-Palacios, K Michael Gibson, Mustafa Sahin, Phillip L Pearl
Clinical and molecular outcomes from the 5-Year natural history study of SSADH Deficiency, a model metabolic neurodevelopmental disorder. Journal of neurodevelopmental disorders 16 (1) (2024)
Itay Tokatly Latzer, Jean-Baptiste Roullet, Wardiya Afshar Saber, Henry Hing Cheong Lee, Mariarita Bertoldi, Gabrielle E McGinty, Melissa L DiBacco, Erland Arning, Melissa Tsuboyama, Alexander Rotenberg, Thomas Opladen, Kathrin Jeltsch, Àngels García-Cazorla, Natalia Juliá-Palacios, K Michael Gibson, Mustafa Sahin, Phillip L Pearl
Clinical and molecular outcomes from the 5-Year natural history study of SSADH Deficiency, a model metabolic neurodevelopmental disorder. Journal of neurodevelopmental disorders 16 (1) (2024)
Henry Hing Cheong Lee, Itay Tokatly Latzer, Mariarita Bertoldi, Guangping Gao, Phillip L Pearl, Mustafa Sahin, Alexander Rotenberg
Gene replacement therapies for inherited disorders of neurotransmission: Current progress in succinic semialdehyde dehydrogenase deficiency. Journal of inherited metabolic disease 47 (3) (2024)
Itay Tokatly Latzer, Jean-Baptiste Roullet, Wardiya Afshar Saber, Henry Hing Cheong Lee, Mariarita Bertoldi, Gabrielle E McGinty, Melissa L DiBacco, Erland Arning, Melissa Tsuboyama, Alexander Rotenberg, Thomas Opladen, Kathrin Jeltsch, Àngels García-Cazorla, Natalia Juliá-Palacios, K Michael Gibson, Mustafa Sahin, Phillip L Pearl
Clinical and molecular outcomes from the 5-Year natural history study of SSADH Deficiency, a model metabolic neurodevelopmental disorder. Journal of neurodevelopmental disorders 16 (1) (2024)
Henry Hing Cheong Lee, Itay Tokatly Latzer, Mariarita Bertoldi, Guangping Gao, Phillip L Pearl, Mustafa Sahin, Alexander Rotenberg
Gene replacement therapies for inherited disorders of neurotransmission: Current progress in succinic semialdehyde dehydrogenase deficiency. Journal of inherited metabolic disease 47 (3) (2024)
Henry Hing Cheong Lee, Itay Tokatly Latzer, Mariarita Bertoldi, Guangping Gao, Phillip L Pearl, Mustafa Sahin, Alexander Rotenberg
Gene replacement therapies for inherited disorders of neurotransmission: Current progress in succinic semialdehyde dehydrogenase deficiency. Journal of inherited metabolic disease 47 (3) (2024)
Henry Hing Cheong Lee, Itay Tokatly Latzer, Mariarita Bertoldi, Guangping Gao, Phillip L Pearl, Mustafa Sahin, Alexander Rotenberg
Gene replacement therapies for inherited disorders of neurotransmission: Current progress in succinic semialdehyde dehydrogenase deficiency. Journal of inherited metabolic disease (2024)
Itay Tokatly Latzer, Jean-Baptiste Roullet, Wardiya Afshar Saber, Henry Hing Cheong Lee, Mariarita Bertoldi, Gabrielle E McGinty, Melissa L DiBacco, Erland Arning, Melissa Tsuboyama, Alexander Rotenberg, Thomas Opladen, Kathrin Jeltsch, Àngels García-Cazorla, Natalia Juliá-Palacios, K Michael Gibson, Mustafa Sahin, Phillip L Pearl
Clinical and molecular outcomes from the 5-Year natural history study of SSADH Deficiency, a model metabolic neurodevelopmental disorder. Journal of neurodevelopmental disorders 16 (1) (2024)
Itay Tokatly Latzer, Jean-Baptiste Roullet, Wardiya Afshar Saber, Henry Hing Cheong Lee, Mariarita Bertoldi, Gabrielle E McGinty, Melissa L DiBacco, Erland Arning, Melissa Tsuboyama, Alexander Rotenberg, Thomas Opladen, Kathrin Jeltsch, Àngels García-Cazorla, Natalia Juliá-Palacios, K Michael Gibson, Mustafa Sahin, Phillip L Pearl
Clinical and molecular outcomes from the 5-Year natural history study of SSADH Deficiency, a model metabolic neurodevelopmental disorder. Journal of neurodevelopmental disorders 16 (1) (2024)
Henry Hing Cheong Lee, Itay Tokatly Latzer, Mariarita Bertoldi, Guangping Gao, Phillip L Pearl, Mustafa Sahin, Alexander Rotenberg
Gene replacement therapies for inherited disorders of neurotransmission: Current progress in succinic semialdehyde dehydrogenase deficiency. Journal of inherited metabolic disease 47 (3) (2024)
Henry Hing Cheong Lee, Itay Tokatly Latzer, Mariarita Bertoldi, Guangping Gao, Phillip L Pearl, Mustafa Sahin, Alexander Rotenberg
Gene replacement therapies for inherited disorders of neurotransmission: Current progress in succinic semialdehyde dehydrogenase deficiency. Journal of inherited metabolic disease (2024)
Itay Tokatly Latzer, Edward Yang, Onur Afacan, Erland Arning, Alexander Rotenberg, Henry Hing Cheong Lee, Jean-Baptiste Roullet, Phillip L Pearl
Glymphatic dysfunction coincides with lower GABA levels and sleep disturbances in succinic semialdehyde dehydrogenase deficiency. Journal of sleep research 33 (4) (2023)
Itay Tokatly Latzer, Jean-Baptiste Roullet, Samuele Cesaro, Melissa L DiBacco, Erland Arning, Alexander Rotenberg, Henry Hing Cheong Lee, Thomas Opladen, Kathrin Jeltsch, Àngels García-Cazorla, Natalia Juliá-Palacios, K Michael Gibson, Mariarita Bertoldi, Phillip L Pearl
Phenotypic correlates of structural and functional protein impairments resultant from ALDH5A1 variants. Human genetics (2023)
Itay Tokatly Latzer, Edward Yang, Onur Afacan, Erland Arning, Alexander Rotenberg, Henry Hing Cheong Lee, Jean-Baptiste Roullet, Phillip L Pearl
Glymphatic dysfunction coincides with lower GABA levels and sleep disturbances in succinic semialdehyde dehydrogenase deficiency. Journal of sleep research 33 (4) (2023)
Itay Tokatly Latzer, Edward Yang, Onur Afacan, Erland Arning, Alexander Rotenberg, Henry Hing Cheong Lee, Jean-Baptiste Roullet, Phillip L Pearl
Glymphatic dysfunction coincides with lower GABA levels and sleep disturbances in succinic semialdehyde dehydrogenase deficiency. Journal of sleep research (2023)
Itay Tokatly Latzer, Edward Yang, Onur Afacan, Erland Arning, Alexander Rotenberg, Henry Hing Cheong Lee, Jean-Baptiste Roullet, Phillip L Pearl
Glymphatic dysfunction coincides with lower GABA levels and sleep disturbances in succinic semialdehyde dehydrogenase deficiency. Journal of sleep research (2023)
Itay Tokatly Latzer, Edward Yang, Onur Afacan, Erland Arning, Alexander Rotenberg, Henry Hing Cheong Lee, Jean-Baptiste Roullet, Phillip L Pearl
Glymphatic dysfunction coincides with lower GABA levels and sleep disturbances in succinic semialdehyde dehydrogenase deficiency. Journal of sleep research (2023)
Mustafa Q Hameed, Nathaniel W Hodgson, Henry Hing Cheong Lee, Andres Pascual-Leone, Paul C MacMullin, Ali Jannati, Sameer C Dhamne, Takao K Hensch, Alexander Rotenberg
N-acetylcysteine treatment mitigates loss of cortical parvalbumin-positive interneuron and perineuronal net integrity resulting from persistent oxidative stress in a rat TBI model. Cerebral cortex (New York, N.Y. : 1991) (2022)
Henry Hing Cheong Lee, Gabrielle E McGinty, Phillip L Pearl, Alexander Rotenberg
Understanding the Molecular Mechanisms of Succinic Semialdehyde Dehydrogenase Deficiency (SSADHD): Towards the Development of SSADH-Targeted Medicine. International journal of molecular sciences 23 (5) (2022)
Henry Hing Cheong Lee, Phillip L Pearl, Alexander Rotenberg
Enzyme Replacement Therapy for Succinic Semialdehyde Dehydrogenase Deficiency: Relevance in γ-Aminobutyric Acid Plasticity. Journal of child neurology 36 (13-14) (2021)