(Q36946663)

17 August 2017

1 reference

title

Brain malformation in syndromic craniosynostoses, a primary disorder of white matter: a review (English)

1 reference

17 August 2017

Charles Raybaud

1

1 reference

17 August 2017

Concezio Di Rocco

series ordinal

2

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17 August 2017

publication date

20 September 2007

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17 August 2017

published in

Child's Nervous System

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17 August 2017

volume

23

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17 August 2017

issue

12

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17 August 2017

page(s)

1379-1388

1 reference

https://scigraph.springernature.com/pub.10.1007/s00381-007-0474-7

17 August 2017

exact match

0 references

cites work

Agenesis of the corpus callosum and limbic malformation in Apert syndrome (type I acrocephalosyndactyly).

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00381-007-0474-7

Apert syndrome: factors involved in the cognitive development.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00381-007-0474-7

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00381-007-0474-7

An updated pediatric perspective on the Apert syndrome.

21 January 2018

1 reference

12 December 2020

The central nervous system in the Apert syndrome

1 reference

12 December 2020

Intracranial anomalies detected by imaging studies in 30 patients with Apert syndrome.

1 reference

12 December 2020

Abnormalities in neuronal process extension, hippocampal development, and the ventricular system of L1 knockout mice.

1 reference

12 December 2020

Clinical variability in patients with Apert's syndrome.

1 reference

12 December 2020

Neural cell adhesion molecule L1: signaling pathways and growth cone motility

1 reference

12 December 2020

Chronic tonsillar herniation in Crouzon's and Apert's syndromes: the role of premature synostosis of the lambdoid suture

1 reference

12 December 2020

Apert and Crouzon syndromes: clinical findings, genes and extracellular matrix.

1 reference

12 December 2020

Pfeiffer syndrome update, clinical subtypes, and guidelines for differential diagnosis

1 reference

12 December 2020

Mutations in the oligophrenin-1 gene (OPHN1) cause X linked congenital cerebellar hypoplasia

1 reference

12 December 2020

Development and malformations of the human pyramidal tract

1 reference

12 December 2020

Cerebral malformations in Carpenter syndrome.

1 reference

12 December 2020

Usefulness of magnetic resonance imaging for accurate diagnosis of Pfeiffer syndrome type II in utero

1 reference

12 December 2020

Favorable prognosis for children with Pfeiffer syndrome types 2 and 3: implications for classification

1 reference

12 December 2020

Crouzon syndrome: phenotypic signs and symptoms of the postnatally expressed subtype

1 reference

12 December 2020

Saethre-Chotzen syndrome: a clinical, EEG and neuroradiological study.

1 reference

12 December 2020

Central nervous system imaging in Crouzon's syndrome.

1 reference

12 December 2020

Apert syndrome: analysis of associated brain malformations and conformational changes determined by surgical treatment

1 reference

12 December 2020

Intellectual development in Apert's syndrome: a long term follow up of 29 patients

1 reference

12 December 2020

Spectrum and detection rate of L1CAM mutations in isolated and familial cases with clinically suspected L1-disease

1 reference

12 December 2020

Development of the perforating pathway: an ipsilaterally projecting pathway between the medial septum/diagonal band of Broca and the cingulate cortex that intersects the corpus callosum.

1 reference

12 December 2020

Pfeiffer syndrome type 2: further delineation and review of the literature

1 reference

12 December 2020

Intellectual outcomes in children and adolescents with syndromic and nonsyndromic craniosynostosis.

1 reference

12 December 2020

Chronic tonsillar herniation and Crouzon's syndrome

1 reference

12 December 2020

Apert's syndrome with central nervous system anomalies

1 reference

12 December 2020

1 reference

12 December 2020

Birth prevalence study of the Apert syndrome

1 reference

12 December 2020

CAM-FGF receptor interactions: a model for axonal growth

1 reference

12 December 2020

Prognosis for mental function in Apert's syndrome

1 reference

12 December 2020

Skull base and calvarial deformities: association with intracranial changes in craniofacial syndromes.

1 reference

12 December 2020

Prenatal diagnosis of craniosynostosis: value of MR imaging.

1 reference

12 December 2020

10.1007/S00381-007-0474-7

Identifiers

DOI

1 reference

17 August 2017

1 reference