about
Absence makes the search grow longerReceptor specificity of the fibroblast growth factor family. The complete mammalian FGF familyCraniosynostosis in Growing Children : Pathophysiological Changes and Neurosurgical ProblemsEpilepsy in Muenke syndrome: FGFR3-related craniosynostosisPleiotropic features of syndromic craniosynostoses correlate with differential expression of fibroblast growth factor receptors 1 and 2 during human craniofacial developmentGuideline for Care of Patients With the Diagnoses of Craniosynostosis: Working Group on CraniosynostosisGrowth and folding of the mammalian cerebral cortex: from molecules to malformationsAnalysis of phenotypic features and FGFR2 mutations in Apert syndrome.Apert syndrome: temporal lobe abnormalities on fetal brain imaging.Impact of genetics on the diagnosis and clinical management of syndromic craniosynostoses.Biochemical analysis of pathogenic ligand-dependent FGFR2 mutations suggests distinct pathophysiological mechanisms for craniofacial and limb abnormalities.Anterior plagiocephaly in an atypical case of apert syndromep.Ser252Trp and p.Pro253Arg mutations in FGFR2 gene causing Apert syndrome: the first clinical and molecular report of Indonesian patients.Novel molecular pathways elicited by mutant FGFR2 may account for brain abnormalities in Apert syndrome.Brain overgrowth in disorders of RTK-PI3K-AKT signaling: a mosaic of malformations.Loss of fibroblast growth factor receptor 2 ligand-binding specificity in Apert syndrome.Differential effects of FGFR2 mutations on syndactyly and cleft palate in Apert syndromeCentral nervous system and cervical spine abnormalities in Apert syndrome.Mesodermal expression of Fgfr2S252W is necessary and sufficient to induce craniosynostosis in a mouse model of Apert syndrome.Deformed Skull Morphology Is Caused by the Combined Effects of the Maldevelopment of Calvarias, Cranial Base and Brain in FGFR2-P253R Mice Mimicking Human Apert Syndrome.The corticospinal tract: Evolution, development, and human disorders.Brain phenotypes in two FGFR2 mouse models for Apert syndrome.The role of sutures in normal and abnormal craniofacial growth.Integration of Brain and Skull in Prenatal Mouse Models of Apert and Crouzon Syndromes.Psychosis in Apert's syndrome with partial agenesis of the corpus callosum.[Apert syndrome in a 60-year old Congolese: about one observation].Sequence analyses and comparative modeling of fly and worm fibroblast growth factor receptors indicate that the determinants for FGF and heparin binding are retained in evolution.Psychosocial functioning in adults with congenital craniofacial conditions.Apert syndrome: magnetic resonance imaging (MRI) of associated intracranial anomalies.Saethre-Chotzen syndrome, Pro136His TWIST mutation, hearing loss, and external and middle ear structural anomalies: report on a Brazilian family.Apert syndrome.Mouse models of Apert syndrome.Mandibular asymmetry in patients with the crouzon or apert syndrome.Cranio-maxillofacial, orthodontic and dental treatment in three patients with Apert syndrome.Comparison of ultrasound and magnetic resonance imaging in the prenatal diagnosis of Apert syndrome: report of a case.Apert syndrome: factors involved in the cognitive development.Computed tomography assessment of Apert syndrome.Apert and Crouzon syndromes-Cognitive development, brain abnormalities, and molecular aspects.Postnatal brain and skull growth in an Apert syndrome mouse model.Central nervous system malformations and deformations in FGFR2-related craniosynostosis.
P2860
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P2860
description
1990 nî lūn-bûn
@nan
1990年の論文
@ja
1990年学术文章
@wuu
1990年学术文章
@zh-cn
1990年学术文章
@zh-hans
1990年学术文章
@zh-my
1990年学术文章
@zh-sg
1990年學術文章
@yue
1990年學術文章
@zh
1990年學術文章
@zh-hant
name
The central nervous system in the Apert syndrome.
@en
type
label
The central nervous system in the Apert syndrome.
@en
prefLabel
The central nervous system in the Apert syndrome.
@en
P2860
P356
P1476
The central nervous system in the Apert syndrome.
@en
P2093
Cohen MM Jr
Kreiborg S
P2860
P356
10.1002/AJMG.1320350108
P577
1990-01-01T00:00:00Z