(Q33184450)

23 July 2017

title

Neuroimaging fails to identify asymptomatic carriers of familial porencephaly (English)

1 reference

23 July 2017

0 references

Vilain C

1

1 reference

23 July 2017

Van Regemorter N

2

1 reference

23 July 2017

Verloes A

3

1 reference

23 July 2017

David P

4

1 reference

23 July 2017

Van Bogaert P

5

1 reference

23 July 2017

publication date

1 October 2002

1 reference

American Journal of Medical Genetics Part A

23 July 2017

published in

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23 July 2017

volume

112

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23 July 2017

issue

2

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23 July 2017

page(s)

198-202

1 reference

Bilateral porencephaly, cerebellar hypoplasia, and internal malformations: two siblings representing a probably new autosomal recessive entity.

23 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10452

Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10452

Factor V Leiden and genetic defects of thrombophilia in childhood porencephaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10452

Familial schizencephaly associated with EMX2 mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10452

Familial schizencephaly: further delineation of a rare disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10452

21 January 2018

Familial schizencephaly

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10452

High risk of cerebral-vein thrombosis in carriers of a prothrombin-gene mutation and in users of oral contraceptives

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10452

Genetic susceptibility to venous thrombosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10452

Factor V Leiden mutation: an unrecognized cause of hemiplegic cerebral palsy, neonatal stroke, and placental thrombosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10452

MRI of patients with cerebral palsy and normal CT scan

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10452

Perisylvian dysgenesis. Clinical, EEG, MRI and glucose metabolism features in 10 patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10452

Familial porencephaly and congenital hemiplegia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10452

21 January 2018

Identifiers

DOI

10.1002/AJMG.10452

1 reference

release_b5etwkmtvvba3eqjoxkszjluui

23 July 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/b5etwkmtvvba3eqjoxkszjluui

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference