Midbrain and hindbrain malformations: advances in clinical diagnosis, imaging, and genetics.
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Brainstem shape is affected by clinical course in the neonatal intensive care unitThe genetics of cerebellar malformationsVariability of Ponto-cerebellar Fibers by Diffusion Tensor Imaging in Diverse Brain Malformations.FGF/FGFR2 signaling regulates the generation and correct positioning of Bergmann glia cells in the developing mouse cerebellumDisorders of Microtubule Function in Neurons: Imaging CorrelatesClinical, neuroradiological and molecular characterization of cerebellar dysplasia with cysts (Poretti-Boltshauser syndrome).Deregulated FGF and homeotic gene expression underlies cerebellar vermis hypoplasia in CHARGE syndrome.Phenotypic outcomes in Mouse and Human Foxc1 dependent Dandy-Walker cerebellar malformation suggest shared mechanisms.Midbrain-Hindbrain Boundary Morphogenesis: At the Intersection of Wnt and Fgf Signaling.Expanding the spectrum of congenital anomalies of the diencephalic-mesencephalic junction.Cerebellar Malformation: Deficits in early neural tube identity found in CHARGE syndrome.Hindbrain malformation and myoclonic seizures associated with a deleterious mutation in the INPP4A gene.Mouse IDGenes: a reference database for genetic interactions in the developing mouse brainPhysiotherapy and Rehabilitation in a Child with Joubert Syndrome.Spectrum of neurodevelopmental disabilities: a cohort study in hungary.Structural and functional outcomes of anaesthetic cornea in children.Ataxia, intellectual disability, and ocular apraxia with cerebellar cysts: a new disease?A morphometric study to establish criteria for fetal and neonatal cerebellar hypoplasia: A special emphasis on trisomy 18.A rare case of cerebellar agenesis: a probabilistic Constrained Spherical Deconvolution tractographic study.RELN and VLDLR mutations underlie two distinguishable clinico-radiological phenotypes.Caudal Fossa Ratio in Normal Dogs and Eurasier Dogs with VLDLR-Associated Genetic Cerebellar Hypoplasia.Cerebellar hypoplasia: differential diagnosis and diagnostic approach.Wnt signal activation induces midbrain specification through direct binding of the beta-catenin/TCF4 complex to the EN1 promoter in human pluripotent stem cells.Clinicoradiological aspects of pontine tegmental cap dysplasia: Case report of a rare hindbrain malformation.
P2860
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P2860
Midbrain and hindbrain malformations: advances in clinical diagnosis, imaging, and genetics.
description
article científic
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article scientifique
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articol științific
@ro
articolo scientifico
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artigo científico
@gl
artigo científico
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artigo científico
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artikel ilmiah
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artikull shkencor
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artículo científico
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name
Midbrain and hindbrain malform ...... gnosis, imaging, and genetics.
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type
label
Midbrain and hindbrain malform ...... gnosis, imaging, and genetics.
@en
prefLabel
Midbrain and hindbrain malform ...... gnosis, imaging, and genetics.
@en
P2860
P1433
P1476
Midbrain and hindbrain malform ...... agnosis, imaging, and genetics
@en
P2093
A James Barkovich
Dan Doherty
P2860
P304
P356
10.1016/S1474-4422(13)70024-3
P577
2013-03-18T00:00:00Z