Autistic-like symptomatology in Prader-Willi syndrome: a review of recent findings (Q36772023)

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scientific article published on April 2007

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Language	Label	Description	Also known as
English	Autistic-like symptomatology in Prader-Willi syndrome: a review of recent findings	scientific article published on April 2007

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

17389128

retrieved

16 August 2017

review article

1 reference

stated in

Europe PubMed Central

title

Autistic-like symptomatology in Prader-Willi syndrome: a review of recent findings (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

17389128

retrieved

16 August 2017

main subject

autism

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Prader–Willi syndrome

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based on heuristic

inferred from title

author name string

Anastasia Dimitropoulos

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

17389128

retrieved

16 August 2017

Robert T Schultz

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

17389128

retrieved

16 August 2017

language of work or name

English

0 references

publication date

1 April 2007

1 reference

stated in

Europe PubMed Central

PubMed publication ID

17389128

retrieved

16 August 2017

published in

Current Psychiatry Reports

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stated in

Europe PubMed Central

PubMed publication ID

17389128

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16 August 2017

volume

9

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stated in

Europe PubMed Central

PubMed publication ID

17389128

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16 August 2017

issue

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

17389128

retrieved

16 August 2017

page(s)

159-164

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Europe PubMed Central

PubMed publication ID

17389128

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16 August 2017

cites work

Pervasive developmental disorders in Prader-Willi syndrome: the Leuven experience in 59 subjects and controls.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1007%2FS11920-007-0086-7

retrieved

21 January 2018

Maladaptive behaviors and risk factors among the genetic subtypes of Prader-Willi syndrome.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1007%2FS11920-007-0086-7

retrieved

21 January 2018

The Yale-Brown Obsessive Compulsive Scale. I. Development, use, and reliability

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1007%2FS11920-007-0086-7

retrieved

21 January 2018

Pervasive developmental disorders and GABAergic system in patients with inverted duplicated chromosome 15.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prader-Willi syndrome: intellectual abilities and behavioural features by genetic subtype

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Emergence of compulsive behavior and tantrums in children with Prader-Willi syndrome.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prader-Willi syndrome

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Compulsive behavior in Prader-Willi syndrome: examining severity in early childhood.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deficits in social attribution ability in Prader-Willi syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism in Angelman syndrome: implications for autism research

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

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12 December 2020

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inferred from PubMed ID database lookup

Maladaptive behavior differences in Prader-Willi syndrome due to paternal deletion versus maternal uniparental disomy

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

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12 December 2020

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inferred from PubMed ID database lookup

Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Obsessions and compulsions in Prader-Willi syndrome

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Problem behaviors and personality of children and adolescents with Prader-Willi syndrome.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Obsessive-compulsive symptoms in Prader-Willi and "Prader-Willi-Like" patients.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

retrieved

12 December 2020

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inferred from PubMed ID database lookup

Maladaptive behaviour in Prader-Willi syndrome in adult life

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Correlates of maladaptive behavior in children and adults with Prader-Willi syndrome

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genetic variant that disrupts MET transcription is associated with autism

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism spectrum disorders in Prader-Willi and Angelman syndromes: a systematic review

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism or atypical autism in maternally but not paternally derived proximal 15q duplication

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Behavioral and emotional symptoms of children and adolescents with Prader-Willi Syndrome

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The phenotypic manifestations of interstitial duplications of proximal 15q with special reference to the autistic spectrum disorders

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The latent variable structure of the Compulsive Behaviour Checklist in people with Prader-Willi syndrome

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Children's Yale-Brown Obsessive Compulsive Scale modified for pervasive developmental disorders

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Repetitive and ritualistic behaviour in children with Prader-Willi syndrome and children with autism

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Research Units on Pediatric Psychopharmacology (RUPP) Autism Network. Background and rationale for an initial controlled study of risperidone.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Three autism candidate genes: a synthesis of human genetic analysis with other disciplines

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Self-injurious behavior and Prader-Willi syndrome: behavioral forms and body locations

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prader-Willi syndrome: atypical psychoses and motor dysfunctions

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A paternally inherited duplication in the Prader-Willi/Angelman syndrome critical region: a case and family study

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Influence of age and tic disorders on obsessive-compulsive disorder in a pediatric sample

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Developmental Behavior Checklist: the development and validation of an instrument to assess behavioral and emotional disturbance in children and adolescents with mental retardation.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prader-Willi syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prader-Willi syndrome--a study comparing deletion and uniparental disomy cases with reference to autism spectrum disorders

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A survey of the phenomenology and pharmacotherapy of compulsive and impulsive-aggressive symptoms in Prader-Willi syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intellectual characteristics of Prader-Willi syndrome: comparison of genetic subtypes.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism screening questionnaire: diagnostic validity

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Obsessive-compulsive disorder in mentally retarded patients.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple pathways regulate MeCP2 expression in normal brain development and exhibit defects in autism-spectrum disorders

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recent advances in the genetics of autism

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17389128

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S11920-007-0086-7

1 reference

stated in

Europe PubMed Central

PubMed publication ID

17389128

retrieved

16 August 2017

PubMed publication ID

17389128

1 reference

stated in

Europe PubMed Central

PubMed publication ID

17389128

retrieved

16 August 2017

ResearchGate publication ID

6418626

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