Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Helen Leonard

Showing results (251-260 of 307) with videos related to

Pageof 31
Sort By:
American Journal of Medical Genetics. Part A|March 26, 2003
Effects of MECP2 mutation type, location and X-inactivation in modulating Rett syndrome phenotypeLinda S Weaving, Sarah L Williamson, Bruce Bennetts, et al.
The Journal of Investigative Dermatology|February 25, 2006
Absence of classical MAP kinase pathway signalling in Merkel cell carcinomaRoland Houben, Barbara Michel, Claudia S Vetter-Kauczok, et al.
European Journal of Pediatrics|December 17, 2018
Epidemiology of gastrostomy insertion for children and adolescents with intellectual disabilityKingsley Wong, Helen Leonard, Glenn Pearson, et al.
The Australian and New Zealand Journal of Psychiatry|June 2, 2020
Prevalence estimates of mental health problems in children and adolescents with intellectual disability: A systematic review and meta-analysisNicholas Buckley, Emma J Glasson, Wai Chen, et al.
Journal of Pediatric Gastroenterology and Nutrition|June 1, 2018
Evolving Trends of Gastrostomy Insertion Within a Pediatric PopulationEmma J Glasson, Kingsley Wong, Helen Leonard, et al.
Journal of Medical Genetics|August 15, 2006
Correlation between clinical severity in patients with Rett syndrome with a p.R168X or p.T158M MECP2 mutation, and the direction and degree of skewing of X-chromosome inactivationHayley Archer, Julie Evans, Helen Leonard, et al.
Pediatric Neurology|April 1, 2019
Cyclin-Dependent Kinase-Like 5 Deficiency Disorder: Clinical ReviewHeather E Olson, Scott T Demarest, Elia M Pestana-Knight, et al.
Intellectual and Developmental Disabilities|October 1, 2019
Data Linkage: Canadian and Australian Perspectives on a Valuable Methodology for Intellectual and Developmental Disability ResearchRobert Balogh, Helen Leonard, Jenny Bourke, et al.
Neurology. Genetics|December 22, 2017
<i>CDKL5</i> variants: Improving our understanding of a rare neurologic disorderRalph D Hector, Vera M Kalscheuer, Friederike Hennig, et al.
European Journal of Epidemiology|March 21, 2019
Birth seasonality and risk of autism spectrum disorderBrian K Lee, Raz Gross, Richard W Francis, et al.
Pageof 31

Showing results (251-260 of 307) with videos related to

Sort By:
Pageof 31
American Journal of Medical Genetics. Part A|March 26, 2003
Effects of MECP2 mutation type, location and X-inactivation in modulating Rett syndrome phenotypeLinda S Weaving, Sarah L Williamson, Bruce Bennetts, et al.
The Journal of Investigative Dermatology|February 25, 2006
Absence of classical MAP kinase pathway signalling in Merkel cell carcinomaRoland Houben, Barbara Michel, Claudia S Vetter-Kauczok, et al.
European Journal of Pediatrics|December 17, 2018
Epidemiology of gastrostomy insertion for children and adolescents with intellectual disabilityKingsley Wong, Helen Leonard, Glenn Pearson, et al.
The Australian and New Zealand Journal of Psychiatry|June 2, 2020
Prevalence estimates of mental health problems in children and adolescents with intellectual disability: A systematic review and meta-analysisNicholas Buckley, Emma J Glasson, Wai Chen, et al.
Journal of Pediatric Gastroenterology and Nutrition|June 1, 2018
Evolving Trends of Gastrostomy Insertion Within a Pediatric PopulationEmma J Glasson, Kingsley Wong, Helen Leonard, et al.
Journal of Medical Genetics|August 15, 2006
Correlation between clinical severity in patients with Rett syndrome with a p.R168X or p.T158M MECP2 mutation, and the direction and degree of skewing of X-chromosome inactivationHayley Archer, Julie Evans, Helen Leonard, et al.
Pediatric Neurology|April 1, 2019
Cyclin-Dependent Kinase-Like 5 Deficiency Disorder: Clinical ReviewHeather E Olson, Scott T Demarest, Elia M Pestana-Knight, et al.
Intellectual and Developmental Disabilities|October 1, 2019
Data Linkage: Canadian and Australian Perspectives on a Valuable Methodology for Intellectual and Developmental Disability ResearchRobert Balogh, Helen Leonard, Jenny Bourke, et al.
Neurology. Genetics|December 22, 2017
<i>CDKL5</i> variants: Improving our understanding of a rare neurologic disorderRalph D Hector, Vera M Kalscheuer, Friederike Hennig, et al.
European Journal of Epidemiology|March 21, 2019
Birth seasonality and risk of autism spectrum disorderBrian K Lee, Raz Gross, Richard W Francis, et al.
Pageof 31