Temporal Lobe Malformations in Achondroplasia: Expanding the Brain Imaging Phenotype Associated with FGFR3-Related Skeletal Dysplasias.

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Temporal Lobe Malformations in Achondroplasia: Expanding the Brain Imaging Phenotype Associated with FGFR3-Related Skeletal Dysplasias.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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name

Temporal Lobe Malformations in ...... 3-Related Skeletal Dysplasias.

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Temporal Lobe Malformations in ...... 3-Related Skeletal Dysplasias.

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label

Temporal Lobe Malformations in ...... 3-Related Skeletal Dysplasias.

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Temporal Lobe Malformations in ...... 3-Related Skeletal Dysplasias.

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Temporal Lobe Malformations in ...... 3-Related Skeletal Dysplasias.

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Temporal Lobe Malformations in ...... 3-Related Skeletal Dysplasias.

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P1476

Temporal Lobe Malformations in ...... R3-Related Skeletal Dysplasias

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P2093

A M Fink

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K B Howell

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K Chetcuti

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R Savarirayan

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S A Mandelstam

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S A Manikkam

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P2860

The molecular and genetic basis of fibroblast growth factor receptor 3 disorders: the achondroplasia family of skeletal dysplasias, Muenke craniosynostosis, and Crouzon syndrome with acanthosis nigricans

Apert syndrome mutations in fibroblast growth factor receptor 2 exhibit increased affinity for FGF ligand

Apert syndrome: temporal lobe abnormalities on fetal brain imaging.

Brain and bone abnormalities of thanatophoric dwarfism.

Health supervision for children with achondroplasia.

Achondroplasia: from genotype to phenotype.

The cerebral cortex malformation in thanatophoric dysplasia: neuropathology and pathogenesis.

Brain malformation in syndromic craniosynostoses, a primary disorder of white matter: a review.

Graded activation of fibroblast growth factor receptor 3 by mutations causing achondroplasia and thanatophoric dysplasia.

Fgf receptor 3 activation promotes selective growth and expansion of occipitotemporal cortex.

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380-384

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scholarly article

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10.3174/AJNR.A5468

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2017-11-23T00:00:00Z

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29170271

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