Itay Tokatly Latzer

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 31

Top Venues

Journal of inherited metabolic disease

Journal of sleep research

Journal of neurodevelopmental disorders

Epilepsia

Edmond and Lily Safra Children's Hospital

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

Affiliation History

Edmond and Lily Safra Children's Hospital Feb 01 2012

Israel

M.D. :: Pediatrics A

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, Ellen Hanson, Mariarita Bertoldi, Ángeles García-Cazorla, Melissa Tsuboyama, Paul MacMullin, Alexander Rotenberg, Jean-Baptiste Roullet, Phillip L Pearl, null null
Autism spectrum disorder and GABA levels in children with succinic semialdehyde dehydrogenase deficiency. Developmental medicine and child neurology (2023)
Itay Tokatly Latzer, Raviv Markovitz, Moran Hausman-Kedem, Shimrit Uliel-Sibony
Treatment of seizures by bloodletting: A call for raised awareness of unfamiliar customs followed by forcibly displaced individuals worldwide. Epileptic disorders : international epilepsy journal with videotape 25 (2) (2023)
Itay Tokatly Latzer, Jean-Baptiste Roullet, K Michael Gibson, Phillip L Pearl
Establishment and Validation of a Clinical Severity Scoring System for Succinic Semialdehyde Dehydrogenase Deficiency. Journal of inherited metabolic disease (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, Mariarita Bertoldi, Melissa L DiBacco, Erland Arning, Melissa Tsuboyama, Paul MacMullin, Daniyal Sachee, Alexander Rotenberg, Henry H C Lee, Deniz Aygun, Thomas Opladen, Kathrin Jeltsch, Àngels García-Cazorla, Jean-Baptiste Roullet, K Michael Gibson, Phillip L Pearl
The Presence and Severity of Epilepsy Coincide with Reduced GABA and Cortical Excitatory Markers in SSADH Deficiency. Epilepsia (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, Raviv Markovitz, Moran Hausman-Kedem, Shimrit Uliel-Sibony
Treatment of seizures by bloodletting: A call for raised awareness of unfamiliar customs followed by forcibly displaced individuals worldwide. Epileptic disorders : international epilepsy journal with videotape 25 (2) (2023)
Itay Tokatly Latzer, Tracey Richmond, Bo Zhang, Phillip L Pearl
Eating disorders occur at high rates in adolescents with epilepsy and are associated with psychiatric comorbidities and suicidality. Epilepsia (2023)
Orit Pinhas-Hamiel, Aya Bardugo, Brian Reichman, Estela Derazne, Zohar Landau, Itay Tokatly Latzer, Liat Lerner-Geva, Jacob Rotschield, Dorit Tzur, Danny Ben-Zvi, Arnon Afek, Gilad Twig
Attention-Deficit Hyperactivity Disorder and Obesity - A National Study of 1.1 Million Israeli Adolescents. The Journal of clinical endocrinology and metabolism (2021)
Itay Tokatly Latzer, Jonathan Roth, Shlomi Constantini, Gustavo Malinger, Alina Weissmann-Brenner, Liat Ben-Sira, Aviva Fattal-Valevski, Hadas Meirson
Neurodevelopmental outcome of children born with an isolated atretic cephalocele. Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery 37 (4) (2021)
Itay Tokatly Latzer, Liora Sagi, Deeksha Sarihyan Bali, Catherine Rehder, Rotem Orbach, Aviva Fattal-Valevski
Variable Genotype-Phenotype Correlation of Pompe's Disease Caused by a c.2015 G > A (p.Arg672Gln) Mutation in the GAA Gene. Neuropediatrics 52 (6) (2021)
Itay Tokatly Latzer, Yael Leitner, Orit Karnieli-Miller
Core experiences of parents of children with autism during the COVID-19 pandemic lockdown. Autism : the international journal of research and practice 25 (4) (2021)
Itay Tokatly Latzer, Rotem Orbach, Liat Ben-Sira, Daphna Mezad-Koursh, Anat Bachar Zipori, Jonathan Roth, Shlomi Constantini, Aviva Fattal-Valevski, Ronit Lubetzky
The Clinical Utility of Inpatient Brain Magnetic Resonance Imaging in Children. Journal of child neurology 35 (11) (2020)
Itay Tokatly Latzer, Amit Blumovich, Liora Sagi, Shimrit Uliel-Sibony, Aviva Fattal-Valevski
Prediction of Drug-Resistant Epilepsy in Children With Cerebral Palsy. Journal of child neurology 35 (3) (2019)
Itay Tokatly Latzer, Liat Lerner-Geva, Daniel Stein, Batia Weiss, Orit Pinhas-Hamiel
Disordered eating behaviors in adolescents with celiac disease. Eating and weight disorders : EWD 25 (2) (2018)

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Publication Activity (10 Years)

Top Topics

Top Venues

Itay Tokatly Latzer