| scholarly article | Q13442814 |
| P356 | DOI | 10.1111/J.1365-2788.2006.00883.X |
| P698 | PubMed publication ID | 17391252 |
| P50 | author | Oscar Vegas | Q56241061 |
| P2093 | author name string | Martinez S | |
| Arias C | |||
| Alén F | |||
| Copet P | |||
| Jauregi J | |||
| Thuilleaux D | |||
| P2860 | cites work | Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy | Q28247810 |
| The genetics of autism | Q28259677 | ||
| Chromosome 15q11-13 abnormalities and other medical conditions in individuals with autism spectrum disorders | Q28277751 | ||
| Is problem solving dependent on language? | Q30350232 | ||
| The Corsi Block-Tapping Task: standardization and normative data. | Q30647260 | ||
| Neuroanatomical substrates of social cognition dysfunction in autism | Q30981179 | ||
| Are jigsaw puzzle skills 'spared' in persons with Prader-Willi syndrome? | Q33337095 | ||
| Weak coherence, no theory of mind, or executive dysfunction? Solving the puzzle of pragmatic language disorders | Q33338380 | ||
| A componential view of theory of mind: evidence from Williams syndrome | Q33902715 | ||
| Cognitive abilities and genotype in a population-based sample of people with Prader-Willi syndrome | Q34289870 | ||
| Minimum prevalence, birth incidence and cause of death for Prader-Willi syndrome in Flanders. | Q34543994 | ||
| Cognitive neuroscience of human social behaviour | Q35075735 | ||
| Prader-Willi syndrome: advances in genetics, pathophysiology and treatment | Q35615332 | ||
| Autism and 15q11-q13 disorders: behavioral, genetic, and pathophysiological issues | Q36017966 | ||
| Prader–Willi syndrome: clinical picture, psychosocial support and current management | Q40549787 | ||
| Strengthening behavioral research on genetic mental retardation syndromes | Q40719924 | ||
| The neuropsychology of autism | Q41115872 | ||
| Are there emotion perception deficits in young autistic children? | Q41226689 | ||
| Population prevalence and estimated birth incidence and mortality rate for people with Prader-Willi syndrome in one UK Health Region | Q43075510 | ||
| An investigation of executive function abilities in adults with Prader-Willi syndrome | Q44282884 | ||
| Prader-Willi syndrome, compulsive and ritualistic behaviours: the first population-based survey | Q44812927 | ||
| Multi-modal P3 deflation of event-related brain activity in Prader-Willi syndrome. | Q48560074 | ||
| The differential contribution of mental tracking, cognitive flexibility, visual search, and motor speed to performance on parts A and B of the Trail Making Test. | Q48716122 | ||
| Pervasive developmental disorder, commonly abbreviated as PDD. | Q50302717 | ||
| Communicative competence and theory of mind in autism: a test of relevance theory. | Q50304914 | ||
| Executive Function Deficits in High-Functioning Autistic Individuals: Relationship to Theory of Mind | Q50306003 | ||
| Ordered-subset analysis of savant skills in autism for 15q11-q13. | Q50306609 | ||
| Deficits in social attribution ability in Prader-Willi syndrome. | Q50307017 | ||
| Autistic spectrum disorder associated with partial duplication of chromosome 15; three case reports. | Q50307094 | ||
| Without a theory of mind one cannot participate in a conversation | Q50307718 | ||
| Longitudinal changes in cognitive and adaptive behavior scores in children and adolescents with the fragile X mutation or autism. | Q50309696 | ||
| Predictors and correlates of adaptive functioning in children with developmental disorders. | Q50310952 | ||
| Continuity and change in the social competence of children with autism, Down syndrome, and developmental delays. | Q50313789 | ||
| Behavioural phenotypes associated with specific genetic disorders: evidence from a population-based study of people with Prader-Willi syndrome. | Q51951077 | ||
| The Rey-Osterrieth Complex Figure as a measure of executive function in childhood. | Q51986936 | ||
| Executive functioning and memory for the Rey-Osterreith complex figure task among community adolescents. | Q51997228 | ||
| Intellectual characteristics of Prader-Willi syndrome: comparison of genetic subtypes. | Q52170199 | ||
| P433 | issue | Pt 5 | |
| P921 | main subject | neuropsychology | Q3872 |
| P304 | page(s) | 350-365 | |
| P577 | publication date | 2007-05-01 | |
| P1433 | published in | Journal of Intellectual Disability Research | Q15757812 |
| P1476 | title | A neuropsychological assessment of frontal cognitive functions in Prader-Willi syndrome | |
| P478 | volume | 51 |
| Q45240690 | Assessment of executive functions in Prader-Willi syndrome and relationship with intellectual level |
| Q50301346 | Behavioral and cognitive phenotype of children and adolescents with Williams-Beuren Syndrome. |
| Q37115306 | Behavioral profile of adults with Prader-Willi syndrome: correlations with individual and environmental variables |
| Q90117068 | Central neurogenetic signatures of the visuomotor integration system |
| Q37346463 | Clinical perspectives on the genetics of schizophrenia: a bottom-up orientation |
| Q89835956 | Equivocal expression of emotions in children with Prader-Willi syndrome: what are the consequences for emotional abilities and social adjustment? |
| Q50311344 | Executive functioning in individuals with intellectual disabilities and autism spectrum disorders. |
| Q57234974 | Fenótipo comportamental de crianças e adolescentes com síndrome de Prader-Willi |
| Q30855592 | French database of children and adolescents with Prader-Willi syndrome |
| Q92537603 | Genotype-Phenotype Relationships and Endocrine Findings in Prader-Willi Syndrome |
| Q36114041 | Imprinted DLK1-DIO3 region of 14q32 defines a schizophrenia-associated miRNA signature in peripheral blood mononuclear cells |
| Q30643463 | Learning by observation and learning by doing in Prader-Willi syndrome |
| Q37445958 | New Perspectives on Genomic Imprinting, an Essential and Multifaceted Mode of Epigenetic Control in the Developing and Adult Brain |
| Q35121153 | Oxytocin may be useful to increase trust in others and decrease disruptive behaviours in patients with Prader-Willi syndrome: a randomised placebo-controlled trial in 24 patients |
| Q34627542 | PET scan perfusion imaging in the Prader-Willi syndrome: new insights into the psychiatric and social disturbances. |
| Q38638685 | Psychotropic treatments in Prader-Willi syndrome: a critical review of published literature |
| Q38925660 | Rigidity in routines and the development of resistance to change in individuals with Prader-Willi syndrome. |
| Q46172096 | Spatial competences in Prader-Willi syndrome: a radial arm maze study |
| Q33409894 | Task-switching deficits and repetitive behaviour in genetic neurodevelopmental disorders: data from children with Prader-Willi syndrome chromosome 15 q11-q13 deletion and boys with Fragile X syndrome |
| Q98283585 | The RDoC approach for translational psychiatry: Could a genetic disorder with psychiatric symptoms help fill the matrix? the example of Prader-Willi syndrome |
| Q48711160 | The relationship between IGF-I concentration, cognitive function and quality of life in adults with Prader-Willi syndrome. |
| Q50650464 | The relationship between specific cognitive impairment and behaviour in Prader-Willi syndrome. |
| Q50795643 | Working memory in Down syndrome: is there a dual task deficit? |
| Q93135379 | [Psychological management of a patient with Prader Willi syndrome: case study of a young Moroccan girl] |
Search more.