(Q50301734)

English

Brief report: autistic behaviors among children with fragile X or Rett syndrome: implications for the classification of pervasive developmental disorder

scientific article published in August 1998

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scholarly article

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Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/9711488

Brief report: autistic behaviors among children with fragile X or Rett syndrome: implications for the classification of pervasive developmental disorder (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/9711488

0 references

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pervasive developmental disorder

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7

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/9711488

author name string

M M Mazzocco

1

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/9711488

M Pulsifer

2

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/9711488

A Fiumara

3

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/9711488

M Cocuzza

4

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/9711488

F Nigro

5

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/9711488

G Incorpora

6

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/9711488

language of work or name

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publication date

1 August 1998

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/9711488

Journal of Autism and Developmental Disorders

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/9711488

28

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Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/9711488

4

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Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/9711488

321-328

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/9711488

Classification of pervasive developmental disorders: some concepts and practical considerations

1 reference

https://pubmed.ncbi.nlm.nih.gov/9711488

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile X syndrome: associated neurological abnormalities and developmental disabilities

1 reference

https://pubmed.ncbi.nlm.nih.gov/9711488

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism is associated with the fragile-X syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/9711488

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autistic symptoms in Rett syndrome: the first two years according to mother reports

1 reference

https://pubmed.ncbi.nlm.nih.gov/9711488

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cerebrospinal fluid biogenic amines and biopterin in Rett syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/9711488

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile X syndrome, DSM-III-R, and autism

1 reference

https://pubmed.ncbi.nlm.nih.gov/9711488

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rett syndrome and the autistic disorders.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9711488

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetics of Rett syndrome: the consequences of a disorder where every case is a new mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/9711488

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Is fragile X syndrome a pervasive developmental disability? Cognitive ability and adaptive behavior in males with the full mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/9711488

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autistic behaviors among girls with fragile X syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9711488

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism: familial aggregation and genetic implications

1 reference

https://pubmed.ncbi.nlm.nih.gov/9711488

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studies of X inactivation and isodisomy in twins provide further evidence that the X chromosome is not involved in Rett syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9711488

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism and the fragile X syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/9711488

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neuroanatomy of Rett syndrome: a volumetric imaging study

1 reference

https://pubmed.ncbi.nlm.nih.gov/9711488

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

AUTISM AND RETT SYNDROME: BEHAVIOURAL INVESTIGATIONS AND DIFFERENTIAL DIAGNOSIS

1 reference

https://pubmed.ncbi.nlm.nih.gov/9711488

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Behavioral phenotype of fragile X syndrome: DSM-III-R autistic behavior in male children

1 reference

https://pubmed.ncbi.nlm.nih.gov/9711488

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cerebellar structure in autism

1 reference

https://pubmed.ncbi.nlm.nih.gov/9711488

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Morphological evidence for brainstem involvement in infantile autism

1 reference

https://pubmed.ncbi.nlm.nih.gov/9711488

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cerebellar and cerebral abnormalities in Rett syndrome: a quantitative MR analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/9711488

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/9711488

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Epidemiology of Rett syndrome: a population-based registry.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9711488

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The borderland of autism and Rett syndrome: five case histories to highlight diagnostic difficulties

1 reference

https://pubmed.ncbi.nlm.nih.gov/9711488

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A behavioral neurogenetics approach to developmental disabilities: gene-brain-behavior associations.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9711488

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pervasive developmental disorders: from DSM-III to DSM-III-R

1 reference

https://pubmed.ncbi.nlm.nih.gov/9711488

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/9711488

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism and genetics. A decade of research

1 reference

https://pubmed.ncbi.nlm.nih.gov/9711488

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypoplasia of Cerebellar Vermal Lobules VI and VII in Autism

1 reference

https://pubmed.ncbi.nlm.nih.gov/9711488

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism in fragile X females

1 reference

https://pubmed.ncbi.nlm.nih.gov/9711488

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Contribution of the FMR1 gene mutation to human intellectual dysfunction

1 reference

https://pubmed.ncbi.nlm.nih.gov/9711488

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1023/A:1026012703449

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/9711488

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/9711488

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