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Journal of Child Neurology
|
February 24, 2001
Mitochondrial DNA point mutation T9176C in Leigh syndrome
C J Wilson, N W Wood, J V Leonard, et al.
Social Neuroscience
|
April 25, 2025
Comparing level 1 and level 2 visuo-spatial perspective-taking in the brain: evidence from fMRI
Matthias Schurz, Matthias G Tholen, Martin Kronbichler, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 14, 1999
GTP cyclohydrolase deficiency; intrafamilial variation in clinical phenotype, including levodopa responsiveness
R Robinson, G T McCarthy, O Bandmann, et al.
Sleep Medicine Reviews
|
May 15, 2018
Sleep duration and sleep quality in people with and without intellectual disability: A meta-analysis
Andrew D R Surtees, Chris Oliver, Chris A Jones, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1993
Physiology and pathophysiology of organic acids in cerebrospinal fluid
G F Hoffmann, W Meier-Augenstein, S Stöckler, et al.
European Journal of Neurology
|
November 29, 2013
Vertical saccade palsy: a presenting sign of Niemann-Pick type IIS
F S Shawkat, L Carr, P West, et al.
Human Molecular Genetics
|
March 1, 1996
Dopa-responsive dystonia in British patients: new mutations of the GTP-cyclohydrolase I gene and evidence for genetic heterogeneity
O Bandmann, T G Nygaard, R Surtees, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
September 9, 2011
The neural and cognitive time course of theory of mind
Joseph P McCleery, Andrew D R Surtees, Katharine A Graham, et al.
Journal of Autism and Developmental Disorders
|
April 3, 2025
Experiencing Independence: Perspectives from Autistic Adults
Piyali Bhattacharya, Rose J Matthews, Rae Field, et al.
Archives of Disease in Childhood
|
October 15, 1998
Clinical and laboratory findings in referrals for mitochondrial DNA analysis
P J Lamont, R Surtees, C E Woodward, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 57) with videos related to
Sort By:
Page
of 6
Journal of Child Neurology
|
February 24, 2001
Mitochondrial DNA point mutation T9176C in Leigh syndrome
C J Wilson, N W Wood, J V Leonard, et al.
Social Neuroscience
|
April 25, 2025
Comparing level 1 and level 2 visuo-spatial perspective-taking in the brain: evidence from fMRI
Matthias Schurz, Matthias G Tholen, Martin Kronbichler, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 14, 1999
GTP cyclohydrolase deficiency; intrafamilial variation in clinical phenotype, including levodopa responsiveness
R Robinson, G T McCarthy, O Bandmann, et al.
Sleep Medicine Reviews
|
May 15, 2018
Sleep duration and sleep quality in people with and without intellectual disability: A meta-analysis
Andrew D R Surtees, Chris Oliver, Chris A Jones, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1993
Physiology and pathophysiology of organic acids in cerebrospinal fluid
G F Hoffmann, W Meier-Augenstein, S Stöckler, et al.
European Journal of Neurology
|
November 29, 2013
Vertical saccade palsy: a presenting sign of Niemann-Pick type IIS
F S Shawkat, L Carr, P West, et al.
Human Molecular Genetics
|
March 1, 1996
Dopa-responsive dystonia in British patients: new mutations of the GTP-cyclohydrolase I gene and evidence for genetic heterogeneity
O Bandmann, T G Nygaard, R Surtees, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
September 9, 2011
The neural and cognitive time course of theory of mind
Joseph P McCleery, Andrew D R Surtees, Katharine A Graham, et al.
Journal of Autism and Developmental Disorders
|
April 3, 2025
Experiencing Independence: Perspectives from Autistic Adults
Piyali Bhattacharya, Rose J Matthews, Rae Field, et al.
Archives of Disease in Childhood
|
October 15, 1998
Clinical and laboratory findings in referrals for mitochondrial DNA analysis
P J Lamont, R Surtees, C E Woodward, et al.
Page
of 6