Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Kathleen Curtiss
A Longitudinal Examination of the Psychoeducational, Neurocognitive, and Psychiatric Functioning in Children With 22q11.2 Deletion Syndrome
Research in Developmental Disabilities
Clinical Psychology
Educational Psychology
Developmental
Discrepancies in Parent and Teacher Ratings of Social-Behavioral Functioning of Children With Chromosome 22q11.2 Deletion Syndrome: Implications for Assessment
American Journal on Intellectual and Developmental Disabilities
Developmental
Arts
Pediatrics
Neuropsychology
Educational Psychology
Humanities
Mental Health
Physiological Psychology
Perinatology
Psychiatry
Neurology
Medicine
Child Health
Related publications
An Examination of the Relationship of Anxiety and Intelligence to Adaptive Functioning in Children With Chromosome 22q11.2 Deletion Syndrome
Journal of Developmental and Behavioral Pediatrics
Developmental
Mental Health
Child Health
Educational Psychology
Perinatology
Psychiatry
Pediatrics
Language Skills in Children With Velocardiofacial Syndrome (Deletion 22q11.2)
Journal of Pediatrics
Child Health
Pediatrics
Perinatology
A New Account of the Neurocognitive Foundations of Impairments in Space, Time, and Number Processing in Children With Chromosome 22q11.2 Deletion Syndrome
Developmental Disabilities Research Reviews
COMT and Anxiety and Cognition in Children With Chromosome 22q11.2 Deletion Syndrome
Psychiatry Research
Psychiatry
Mental Health
Biological Psychiatry
Childhood Predictors of Written Expression in Late Adolescents With 22q11.2 Deletion Syndrome: A Longitudinal Study
Journal of Intellectual Disability Research
Mental Health
Humanities
Arts
Neurology
Psychiatry
Rehabilitation
Cognitive Correlates of a Functional COMT Polymorphism in Children With 22q11.2 Deletion Syndrome
Clinical Genetics
Genetics
Acute Dystonia in a Patient With 22q11.2 Deletion Syndrome
Mental Illness
Psychiatry
Mental Health
Obesity in Adults With 22q11.2 Deletion Syndrome
Genetics in Medicine
Medicine
Genetics