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Journal of Pediatric Gastroenterology and Nutrition
|
February 15, 2012
Gastrointestinal and nutritional problems occur frequently throughout life in girls and women with Rett syndrome
Kathleen J Motil, Erwin Caeg, Judy O Barrish, et al.
Plos One
|
November 10, 2016
Loss of MeCP2 Causes Urological Dysfunction and Contributes to Death by Kidney Failure in Mouse Models of Rett Syndrome
Christopher S Ward, Teng-Wei Huang, José A Herrera, et al.
Science Translational Medicine
|
December 17, 2011
Pathogenesis of lethal cardiac arrhythmias in Mecp2 mutant mice: implication for therapy in Rett syndrome
Mark D McCauley, Tiannan Wang, Elise Mike, et al.
Pediatric Research
|
December 25, 2009
Profiling scoliosis in Rett syndrome
Alan K Percy, Hye-Seung Lee, Jeffrey L Neul, et al.
Annals of Neurology
|
November 25, 2010
Rett syndrome diagnostic criteria: lessons from the Natural History Study
Alan K Percy, Jeffrey L Neul, Daniel G Glaze, et al.
Brain & Development
|
April 17, 2018
The course of awake breathing disturbances across the lifespan in Rett syndrome
Daniel C Tarquinio, Wei Hou, Jeffrey L Neul, et al.
Annals of Neurology
|
December 15, 2010
Rett syndrome: revised diagnostic criteria and nomenclature
Jeffrey L Neul, Walter E Kaufmann, Daniel G Glaze, et al.
Neurology
|
October 5, 2012
Growth failure and outcome in Rett syndrome: specific growth references
Daniel Charles Tarquinio, Kathleen J Motil, Wei Hou, 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 syndrome
Christopher A Chapleau, Jane Lane, Susan M Kirwin, et al.
Journal of Neurodevelopmental Disorders
|
July 30, 2014
Developmental delay in Rett syndrome: data from the natural history study
Jeffrey L Neul, Jane B Lane, Hye-Seung Lee, et al.
Page
of 11
Search research articles
Search
Showing results (71-80 of 107) with videos related to
Sort By:
Page
of 11
Journal of Pediatric Gastroenterology and Nutrition
|
February 15, 2012
Gastrointestinal and nutritional problems occur frequently throughout life in girls and women with Rett syndrome
Kathleen J Motil, Erwin Caeg, Judy O Barrish, et al.
Plos One
|
November 10, 2016
Loss of MeCP2 Causes Urological Dysfunction and Contributes to Death by Kidney Failure in Mouse Models of Rett Syndrome
Christopher S Ward, Teng-Wei Huang, José A Herrera, et al.
Science Translational Medicine
|
December 17, 2011
Pathogenesis of lethal cardiac arrhythmias in Mecp2 mutant mice: implication for therapy in Rett syndrome
Mark D McCauley, Tiannan Wang, Elise Mike, et al.
Pediatric Research
|
December 25, 2009
Profiling scoliosis in Rett syndrome
Alan K Percy, Hye-Seung Lee, Jeffrey L Neul, et al.
Annals of Neurology
|
November 25, 2010
Rett syndrome diagnostic criteria: lessons from the Natural History Study
Alan K Percy, Jeffrey L Neul, Daniel G Glaze, et al.
Brain & Development
|
April 17, 2018
The course of awake breathing disturbances across the lifespan in Rett syndrome
Daniel C Tarquinio, Wei Hou, Jeffrey L Neul, et al.
Annals of Neurology
|
December 15, 2010
Rett syndrome: revised diagnostic criteria and nomenclature
Jeffrey L Neul, Walter E Kaufmann, Daniel G Glaze, et al.
Neurology
|
October 5, 2012
Growth failure and outcome in Rett syndrome: specific growth references
Daniel Charles Tarquinio, Kathleen J Motil, Wei Hou, 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 syndrome
Christopher A Chapleau, Jane Lane, Susan M Kirwin, et al.
Journal of Neurodevelopmental Disorders
|
July 30, 2014
Developmental delay in Rett syndrome: data from the natural history study
Jeffrey L Neul, Jane B Lane, Hye-Seung Lee, et al.
Page
of 11