(Q41918389)

14 October 2017

Genotype and natural history in unrelated individuals with phenylketonuria and autistic behavior (English)

1 reference

14 October 2017

0 references

1 reference

Carlos Eduardo Steiner

1

1 reference

14 October 2017

Angelina Xavier Acosta

2

1 reference

14 October 2017

Marilisa Mantovani Guerreiro

3

1 reference

14 October 2017

Antonia Paula Marques-de-Faria

4

1 reference

14 October 2017

1 June 2007

1 reference

Arquivos de Neuro-Psiquiatria

14 October 2017

1 reference

14 October 2017

65

1 reference

14 October 2017

2A

1 reference

14 October 2017

202-205

1 reference

Metabolic approaches to the treatment of autism spectrum disorders.

14 October 2017

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2007000200003

The neurobiology of infantile autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2007000200003

Genetic and neurological evaluation in a sample of individuals with pervasive developmental disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2007000200003

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2007000200003

Mutations of the phenylalanine hydroxylase (PAH) gene in Brazilian patients with phenylketonuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2007000200003

Detection of phenylketonuria in autistic and psychotic children.

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2007000200003

Autism and mental retardation: neuropathologic studies performed in four retarded persons with autistic behavior.

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2007000200003

A Chinese classic phenylketonuria manifested as autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2007000200003

Phenylketonuria: an underlying etiology of autistic syndrome. A case report

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2007000200003

Autism and phenylketonuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2007000200003

Autism and genetic disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2007000200003

Phenylketonuria: genotype-phenotype correlations based on expression analysis of structural and functional mutations in PAH.

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2007000200003

The STR252-IVS10nt546-VNTR7 phenylalanine hydroxylase minihaplotype in five Mediterranean samples

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2007000200003

Molecular characterization of phenylketonuria in South Brazil

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2007000200003

Population genetics of hyperphenylalaninaemia resulting from phenylalanine hydroxylase deficiency in Portugal

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2007000200003

10.1590/S0004-282X2007000200003

21 January 2018

Identifiers

DOI

1 reference

14 October 2017

1 reference