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Patrick F Bolton

Showing results (41-50 of 66) with videos related to

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Developmental Medicine and Child Neurology|September 21, 2019
Long-term cognitive outcomes in tuberous sclerosis complexCharlotte Tye, Fiona S Mcewen, Holan Liang, et al.
Journal of Autism and Developmental Disorders|March 31, 2005
A paternally inherited duplication in the Prader-Willi/Angelman syndrome critical region: a case and family studyMarijcke W M Veltman, Russell J Thompson, Ellen E Craig, et al.
Epilepsia|January 15, 2014
Intellectual development before and after the onset of infantile spasms: a controlled prospective longitudinal study in tuberous sclerosisAyla Humphrey, Cathy MacLean, George B Ploubidis, et al.
Epilepsia|January 12, 2023
Epilepsy severity mediates association between mutation type and ADHD symptoms in tuberous sclerosis complexCharlotte Tye, Fiona S McEwen, Holan Liang, et al.
Archives of Disease in Childhood|August 5, 2011
The Tuberous Sclerosis 2000 Study: presentation, initial assessments and implications for diagnosis and managementJohn R W Yates, Cathy Maclean, J Nicholas P Higgins, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines|September 24, 2005
Prader-Willi syndrome: intellectual abilities and behavioural features by genetic subtypeKatja M Milner, Ellen E Craig, Russell J Thompson, et al.
Journal of Neurodevelopmental Disorders|January 18, 2014
Associations of HLA alleles with specific language impairmentRon Nudel, Nuala H Simpson, Gillian Baird, et al.
Autism Research : Official Journal of the International Society for Autism Research|April 28, 2016
Screening for co-occurring conditions in adults with autism spectrum disorder using the strengths and difficulties questionnaire: A pilot studyJames Findon, Tim Cadman, Catherine S Stewart, et al.
European Journal of Human Genetics : EJHG|January 15, 2015
Genome-wide analysis identifies a role for common copy number variants in specific language impairmentNuala H Simpson, Fabiola Ceroni, Rose H Reader, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|April 17, 2021
Systematic Review and Meta-analysis: The Science of Early-Life Precursors and Interventions for Attention-Deficit/Hyperactivity DisorderElizabeth Shephard, Pedro F Zuccolo, Iman Idrees, et al.
Pageof 7

Showing results (41-50 of 66) with videos related to

Sort By:
Pageof 7
Developmental Medicine and Child Neurology|September 21, 2019
Long-term cognitive outcomes in tuberous sclerosis complexCharlotte Tye, Fiona S Mcewen, Holan Liang, et al.
Journal of Autism and Developmental Disorders|March 31, 2005
A paternally inherited duplication in the Prader-Willi/Angelman syndrome critical region: a case and family studyMarijcke W M Veltman, Russell J Thompson, Ellen E Craig, et al.
Epilepsia|January 15, 2014
Intellectual development before and after the onset of infantile spasms: a controlled prospective longitudinal study in tuberous sclerosisAyla Humphrey, Cathy MacLean, George B Ploubidis, et al.
Epilepsia|January 12, 2023
Epilepsy severity mediates association between mutation type and ADHD symptoms in tuberous sclerosis complexCharlotte Tye, Fiona S McEwen, Holan Liang, et al.
Archives of Disease in Childhood|August 5, 2011
The Tuberous Sclerosis 2000 Study: presentation, initial assessments and implications for diagnosis and managementJohn R W Yates, Cathy Maclean, J Nicholas P Higgins, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines|September 24, 2005
Prader-Willi syndrome: intellectual abilities and behavioural features by genetic subtypeKatja M Milner, Ellen E Craig, Russell J Thompson, et al.
Journal of Neurodevelopmental Disorders|January 18, 2014
Associations of HLA alleles with specific language impairmentRon Nudel, Nuala H Simpson, Gillian Baird, et al.
Autism Research : Official Journal of the International Society for Autism Research|April 28, 2016
Screening for co-occurring conditions in adults with autism spectrum disorder using the strengths and difficulties questionnaire: A pilot studyJames Findon, Tim Cadman, Catherine S Stewart, et al.
European Journal of Human Genetics : EJHG|January 15, 2015
Genome-wide analysis identifies a role for common copy number variants in specific language impairmentNuala H Simpson, Fabiola Ceroni, Rose H Reader, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|April 17, 2021
Systematic Review and Meta-analysis: The Science of Early-Life Precursors and Interventions for Attention-Deficit/Hyperactivity DisorderElizabeth Shephard, Pedro F Zuccolo, Iman Idrees, et al.
Pageof 7