(Q50310770)

2 March 2018

title

Autism spectrum conditions in myotonic dystrophy type 1: a study on 57 individuals with congenital and childhood forms. (English)

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2 March 2018

main subject

autism spectrum disorder

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Anne-Berit Ekström

1

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2 March 2018

Louise Hakenäs-Plate

2

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2 March 2018

Lena Samuelsson

3

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2 March 2018

Már Tulinius

4

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2 March 2018

Elisabet Wentz

5

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2 March 2018

publication date

1 September 2008

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2 March 2018

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

published in

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2 March 2018

volume

147B

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2 March 2018

issue

6

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2 March 2018

page(s)

918-926

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2 March 2018

Differential effects of developmental cerebellar abnormality on cognitive and motor functions in the cerebellum: an fMRI study of autism.

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21 January 2018

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ETR-3 represses Tau exons 2/3 inclusion, a splicing event abnormally enhanced in myotonic dystrophy type I.

21 January 2018

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Failure of MBNL1-dependent post-natal splicing transitions in myotonic dystrophy

21 January 2018

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Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Sleep disorders in childhood-onset myotonic dystrophy type 1.

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.30698

RNA-mediated neuromuscular disorders

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.30698

Converging evidence for brain stem injury in autism

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.30698

The behavioral phenotype in fragile X: symptoms of autism in very young children with fragile X syndrome, idiopathic autism, and other developmental disorders.

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.30698

Presentation, clinical course, and outcome of the congenital form of myotonic dystrophy

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.30698

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.30698

Neuroradiological findings in children with congenital myotonic dystrophy

21 January 2018

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Brain alterations in the classical form of congenital muscular dystrophy. Clinical and neuroimaging follow-up of 12 cases and correlation with the expression of merosin in muscle.

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Temperament and character in patients with classical myotonic dystrophy type 1 (DM-1).

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.30698

21 January 2018

The autistic spectrum

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.30698

Childhood autism and associated comorbidities

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.30698

Asperger syndrome associated with Steinert's myotonic dystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.30698

21 January 2018

Identifiers

DOI

10.1002/AJMG.B.30698

1 reference

2 March 2018

PubMed ID

18228241

1 reference

2 March 2018