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Jeffrey L Neul

Showing results (81-90 of 122) with videos related to

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Annals of Neurology|November 25, 2010
Rett syndrome diagnostic criteria: lessons from the Natural History StudyAlan K Percy, Jeffrey L Neul, Daniel G Glaze, et al.
Annals of Neurology|December 15, 2010
Rett syndrome: revised diagnostic criteria and nomenclatureJeffrey L Neul, Walter E Kaufmann, Daniel G Glaze, et al.
Brain & Development|April 17, 2018
The course of awake breathing disturbances across the lifespan in Rett syndromeDaniel C Tarquinio, Wei Hou, Jeffrey L Neul, et al.
Journal of Neurodevelopmental Disorders|July 30, 2014
Developmental delay in Rett syndrome: data from the natural history studyJeffrey L Neul, Jane B Lane, Hye-Seung Lee, et al.
Genes|August 29, 2024
Clinical Features and Disease Progression in Older Individuals with Rett SyndromeJeffrey L Neul, Timothy A Benke, Eric D Marsh, et al.
American Journal of Medical Genetics. Part A|May 23, 2013
Detection of rarely identified multiple mutations in MECP2 gene do not contribute to enhanced severity in Rett syndromeChristopher A Chapleau, Jane Lane, Susan M Kirwin, et al.
Annals of Neurology|May 9, 2024
Electroencephalographic Correlates of Clinical Severity in the Natural history study of RTT and Related DisordersJoni N Saby, Patrick J Mulcahey, Timothy A Benke, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 13, 2016
Enrichment of mutations in chromatin regulators in people with Rett syndrome lacking mutations in MECP2Samin A Sajan, Shalini N Jhangiani, Donna M Muzny, et al.
Nature|November 12, 2010
Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypesHsiao-Tuan Chao, Hongmei Chen, Rodney C Samaco, et al.
Medrxiv : the Preprint Server for Health Sciences|August 8, 2025
Altered oscillatory coupling reflects possible inhibitory interneuron dysfunction in Rett syndromeDevorah Kranz, Yael Braverman, Michelle McCarthy, et al.
Pageof 13

Showing results (81-90 of 122) with videos related to

Sort By:
Pageof 13
Annals of Neurology|November 25, 2010
Rett syndrome diagnostic criteria: lessons from the Natural History StudyAlan K Percy, Jeffrey L Neul, Daniel G Glaze, et al.
Annals of Neurology|December 15, 2010
Rett syndrome: revised diagnostic criteria and nomenclatureJeffrey L Neul, Walter E Kaufmann, Daniel G Glaze, et al.
Brain & Development|April 17, 2018
The course of awake breathing disturbances across the lifespan in Rett syndromeDaniel C Tarquinio, Wei Hou, Jeffrey L Neul, et al.
Journal of Neurodevelopmental Disorders|July 30, 2014
Developmental delay in Rett syndrome: data from the natural history studyJeffrey L Neul, Jane B Lane, Hye-Seung Lee, et al.
Genes|August 29, 2024
Clinical Features and Disease Progression in Older Individuals with Rett SyndromeJeffrey L Neul, Timothy A Benke, Eric D Marsh, et al.
American Journal of Medical Genetics. Part A|May 23, 2013
Detection of rarely identified multiple mutations in MECP2 gene do not contribute to enhanced severity in Rett syndromeChristopher A Chapleau, Jane Lane, Susan M Kirwin, et al.
Annals of Neurology|May 9, 2024
Electroencephalographic Correlates of Clinical Severity in the Natural history study of RTT and Related DisordersJoni N Saby, Patrick J Mulcahey, Timothy A Benke, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 13, 2016
Enrichment of mutations in chromatin regulators in people with Rett syndrome lacking mutations in MECP2Samin A Sajan, Shalini N Jhangiani, Donna M Muzny, et al.
Nature|November 12, 2010
Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypesHsiao-Tuan Chao, Hongmei Chen, Rodney C Samaco, et al.
Medrxiv : the Preprint Server for Health Sciences|August 8, 2025
Altered oscillatory coupling reflects possible inhibitory interneuron dysfunction in Rett syndromeDevorah Kranz, Yael Braverman, Michelle McCarthy, et al.
Pageof 13