Charuta G Furey

发表

Case Report: Internal Carotid Artery Thrombosis: A Rare Complication After Fibrin Glue Injection for Cavernous Sinus Hemostasis

M. Lawton, J. Hernesniemi, V. Srinivasan, 2021, Frontiers in Surgery.

Mutations in Chromatin Modifier and Ephrin Signaling Genes in Vein of Galen Malformation

Edward R. Smith, Mark W. Youngblood, I. Tikhonova, 2019, Neuron.

Mutations in chromatin modifiers and Ephrin signaling components in Vein of Galen malformation

Edward R. Smith, Mark W. Youngblood, Weilai, 2019 .

Impaired neurogenesis alters brain biomechanics in a neuroprogenitor-based genetic subtype of congenital hydrocephalus

P. Rakic, R. Constable, N. Šestan, 2022, Nature Neuroscience.

Exome Sequencing Implicates Impaired GABA Signaling and Neuronal Ion Transport in Trigeminal Neuralgia

J. Gerrard, S. Mane, J. Simard, 2020, iScience.

Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalus

Edward R. Smith, D. Geschwind, J. Broach, 2020, Nature Medicine.

De novo mutations in inhibitors of Wnt, BMP, and Ras/ERK signaling pathways in non-syndromic midline craniosynostosis

R. Lifton, C. Nelson-Williams, K. Kahle, 2017, Proceedings of the National Academy of Sciences.

De Novo Mutation in Genes Regulating Neural Stem Cell Fate in Human Congenital Hydrocephalus

Edward R. Smith, S. Mane, R. Bjornson, 2018, Neuron.

Inflammation-dependent cerebrospinal fluid hypersecretion by the choroid plexus epithelium in posthemorrhagic hydrocephalus

J. Simard, M. Gunel, R. Medzhitov, 2017, Nature Medicine.

Xp22.2 Chromosomal Duplication in Familial Intracranial Arachnoid Cyst

C. Nelson-Williams, K. Kahle, Peining Li, 2017, JAMA neurology.

9p24 triplication in syndromic hydrocephalus with diffuse villous hyperplasia of the choroid plexus

M. Günel, C. Nelson-Williams, C. Matouk, 2018, Cold Spring Harbor molecular case studies.

Magnetic Resonance-Guided Laser Interstitial Thermal Therapy for Management of Low-Grade Gliomas and Radiation Necrosis: A Single-Institution Case Series

Dara S. Farhadi, Jubran H. Jubran, Kris A Smith, 2022, Brain sciences.

Co-occurrence of frameshift mutations in SMAD6 and TCF12 in a child with complex craniosynostosis

R. Lifton, C. Nelson-Williams, J. Persing, 2018, Human Genome Variation.

The "Binder Ring" Bypass: Transection, Rerouting, and Reanastomosis as an Alternative to Macrovascular Decompression of a Dolichoectatic Vertebral Artery.

M. Lawton, J. Catapano, V. Srinivasan, 2022, Operative neurosurgery.

Far Lateral Approach for Resection of a Calcifying Pseudoneoplasm of the Neuroaxis: 2-Dimensional Operative Video.

M. Lawton, V. Srinivasan, C. Furey, 2023, Operative neurosurgery.

Multiomic analyses implicate a neurodevelopmental program in the pathogenesis of cerebral arachnoid cysts

Shrikant Mane, R. Lifton, C. Nelson-Williams, 2023, Nature Medicine.

Residual Tumor Volume and Tumor Progression after Subtotal Resection and Observation of WHO Grade I Skull Base Meningiomas

N. Sanai, A. Little, B. Hendricks, 2021, Journal of Neurological Surgery Part B: Skull Base.

Visualizing flow in an intact CSF network using optical coherence tomography: implications for human congenital hydrocephalus

M. Khokha, K. Kahle, Stephan M. Jonas, 2019, Scientific Reports.

Congenital Hydrocephalus

K. Kahle, Prince Antwi, C. Furey, 2018, Cerebrospinal Fluid Disorders.