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European Journal of Human Genetics : EJHG
|
April 5, 2012
The phenotype associated with a large deletion on MECP2
Ami Bebbington, Jenny Downs, Alan Percy, et al.
American Journal of Medical Genetics. Part A
|
April 2, 2004
Phenotypic manifestations of MECP2 mutations in classical and atypical Rett syndrome
Carolyn Schanen, Elisa J F Houwink, Naghmeh Dorrani, et al.
Epilepsy Research
|
August 29, 2025
Natural history of epilepsy in FOXG1 Syndrome
Caleb Rhodes, Benjamin Rees, Holly Dubbs, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
October 15, 2013
Gastrointestinal dysmotility in Rett syndrome
Gordon Baikie, Madhur Ravikumara, Jenny Downs, et al.
Annals of Neurology
|
May 31, 2020
Comparison of Core Features in Four Developmental Encephalopathies in the Rett Natural History Study
Clare Cutri-French, Dallas Armstrong, Joni Saby, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
October 3, 2013
Assessment and management of nutrition and growth in Rett syndrome
Helen Leonard, Madhur Ravikumara, Gordon Baikie, et al.
Pediatric Neurology
|
October 2, 2017
A Double-Blind, Randomized, Placebo-Controlled Clinical Study of Trofinetide in the Treatment of Rett Syndrome
Daniel G Glaze, Jeffrey L Neul, Alan Percy, et al.
Research in Autism Spectrum Disorders
|
December 19, 2013
InterRett, a model for international data collection in a rare genetic disorder
Sandra Louise, Sue Fyfe, Ami Bebbington, et al.
Journal of Neurodevelopmental Disorders
|
January 25, 2025
A randomized, placebo-controlled, cross-over trial of ketamine in Rett syndrome
Kathleen Campbell, Jeffrey L Neul, David N Lieberman, et al.
BMJ Paediatrics Open
|
October 7, 2020
Multisystem comorbidities in classic Rett syndrome: a scoping review
Cary Fu, Dallas Armstrong, Eric Marsh, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 17) with videos related to
Sort By:
Page
of 2
European Journal of Human Genetics : EJHG
|
April 5, 2012
The phenotype associated with a large deletion on MECP2
Ami Bebbington, Jenny Downs, Alan Percy, et al.
American Journal of Medical Genetics. Part A
|
April 2, 2004
Phenotypic manifestations of MECP2 mutations in classical and atypical Rett syndrome
Carolyn Schanen, Elisa J F Houwink, Naghmeh Dorrani, et al.
Epilepsy Research
|
August 29, 2025
Natural history of epilepsy in FOXG1 Syndrome
Caleb Rhodes, Benjamin Rees, Holly Dubbs, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
October 15, 2013
Gastrointestinal dysmotility in Rett syndrome
Gordon Baikie, Madhur Ravikumara, Jenny Downs, et al.
Annals of Neurology
|
May 31, 2020
Comparison of Core Features in Four Developmental Encephalopathies in the Rett Natural History Study
Clare Cutri-French, Dallas Armstrong, Joni Saby, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
October 3, 2013
Assessment and management of nutrition and growth in Rett syndrome
Helen Leonard, Madhur Ravikumara, Gordon Baikie, et al.
Pediatric Neurology
|
October 2, 2017
A Double-Blind, Randomized, Placebo-Controlled Clinical Study of Trofinetide in the Treatment of Rett Syndrome
Daniel G Glaze, Jeffrey L Neul, Alan Percy, et al.
Research in Autism Spectrum Disorders
|
December 19, 2013
InterRett, a model for international data collection in a rare genetic disorder
Sandra Louise, Sue Fyfe, Ami Bebbington, et al.
Journal of Neurodevelopmental Disorders
|
January 25, 2025
A randomized, placebo-controlled, cross-over trial of ketamine in Rett syndrome
Kathleen Campbell, Jeffrey L Neul, David N Lieberman, et al.
BMJ Paediatrics Open
|
October 7, 2020
Multisystem comorbidities in classic Rett syndrome: a scoping review
Cary Fu, Dallas Armstrong, Eric Marsh, et al.
Page
of 2