Brain malformation in syndromic craniosynostoses, a primary disorder of white matter: a review.
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Update of Diagnostic Evaluation of Craniosynostosis with a Focus on Pediatric Systematic Evaluation and Genetic StudiesCraniosynostosis in Growing Children : Pathophysiological Changes and Neurosurgical ProblemsApert syndrome: temporal lobe abnormalities on fetal brain imaging.Skull base development and craniosynostosis.Neuroimaging Findings in Pediatric Genetic Skeletal Disorders: A Review.Recessive mutations in the gene encoding the tight junction protein occludin cause band-like calcification with simplified gyration and polymicrogyria.Novel molecular pathways elicited by mutant FGFR2 may account for brain abnormalities in Apert syndrome.Brain and ventricular volume in patients with syndromic and complex craniosynostosis.Investigation of TBR1 Hemizygosity: Four Individuals with 2q24 MicrodeletionsMesodermal expression of Fgfr2S252W is necessary and sufficient to induce craniosynostosis in a mouse model of Apert syndrome.The FGF family: biology, pathophysiology and therapyAstroglial-Mediated Remodeling of the Interhemispheric Midline Is Required for the Formation of the Corpus CallosumCrouzon syndrome with primary optic nerve atrophy and normal brain functions: A case report.Craniosynostosis genetics: The mystery unfolds.Radial Structure Scaffolds Convolution Patterns of Developing Cerebral Cortex.The corticospinal tract: Evolution, development, and human disorders.Apert syndrome: magnetic resonance imaging (MRI) of associated intracranial anomalies.Temporal Lobe Malformations in Achondroplasia: Expanding the Brain Imaging Phenotype Associated with FGFR3-Related Skeletal Dysplasias.Diffusion Tensor Imaging and Fiber Tractography in Children with Craniosynostosis Syndromes.Saethre-Chotzen syndrome, Pro136His TWIST mutation, hearing loss, and external and middle ear structural anomalies: report on a Brazilian family.Mouse models of Apert syndrome.Apert syndrome with fused thalami.Clinical and neuroradiological features of the 9p deletion syndrome.Apert and Crouzon syndromes-Cognitive development, brain abnormalities, and molecular aspects.Central nervous system malformations and deformations in FGFR2-related craniosynostosis.The Unnecessity of Positron Emission Tomography Computed Tomography in the Etiologic Evaluation of Neurodevelopmental Delay in Craniosynostosis PatientsAsymmetric laterality of Chiari type I malformation in patients with non-syndromic single-suture craniosynostosisCloverleaf skull deformity and hydrocephalusMuenke syndrome with pigmentary disorder and probable hemimegalencephaly: An expansion of the phenotype
P2860
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P2860
Brain malformation in syndromic craniosynostoses, a primary disorder of white matter: a review.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Brain malformation in syndromi ...... der of white matter: a review.
@en
type
label
Brain malformation in syndromi ...... der of white matter: a review.
@en
prefLabel
Brain malformation in syndromi ...... der of white matter: a review.
@en
P2860
P1476
Brain malformation in syndromi ...... der of white matter: a review.
@en
P2093
Charles Raybaud
Concezio Di Rocco
P2860
P2888
P304
P356
10.1007/S00381-007-0474-7
P577
2007-09-20T00:00:00Z