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AXIN1 mutations in nonsyndromic craniosynostosis.
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- Journal of Neurosurgery: Pediatrics, 2024, v. 34, n. 3, p. 246, doi. 10.3171/2024.5.PEDS24115
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- Article
Inflammatory hydrocephalus.
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- Child's Nervous System, 2021, v. 37, n. 11, p. 3341, doi. 10.1007/s00381-021-05255-z
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- Article
Genomics of human congenital hydrocephalus.
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- Child's Nervous System, 2021, v. 37, n. 11, p. 3325, doi. 10.1007/s00381-021-05230-8
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- Article
Pre-operative headaches and obstructive hydrocephalus predict an extended length of stay following suboccipital decompression for pediatric Chiari I malformation.
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- Child's Nervous System, 2021, v. 37, n. 1, p. 91, doi. 10.1007/s00381-020-04688-2
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- Publication type:
- Article
Non-syndromic single-suture craniosynostosis in triplets.
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- Child's Nervous System, 2018, v. 34, n. 6, p. 1241, doi. 10.1007/s00381-018-3754-5
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- Article
The KCC2 Cotransporter and Human Epilepsy.
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- Neuroscientist, 2016, v. 22, n. 6, p. 555, doi. 10.1177/1073858416645087
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- Article
The GABA Excitatory/Inhibitory Shift in Brain Maturation and Neurological Disorders.
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- Neuroscientist, 2012, v. 18, n. 5, p. 467, doi. 10.1177/1073858412438697
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- Article
Malignant Cerebellar edema subsequent to accidental prescription opioid Intoxication in Children.
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- Frontiers in Neurology, 2017, p. 1, doi. 10.3389/fneur.2017.00362
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- Publication type:
- Article
Trends in inpatient setting laminectomy for excision of herniated intervertebral disc: Population-based estimates from the US nationwide inpatient sample.
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- Surgical Neurology International, 2011, v. 2, n. 1, p. 25, doi. 10.4103/2152-7806.76144
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- Article
Algebraic Nexus of Fibonacci Forms and Two-Simplex Topology in Multicellular Morphogenesis.
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- Symmetry (20738994), 2024, v. 16, n. 5, p. 516, doi. 10.3390/sym16050516
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- Publication type:
- Article
Cation flux through SUR1-TRPM4 and NCX1 in astrocyte endfeet induces water influx through AQP4 and brain swelling after ischemic stroke.
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- Science Signaling, 2023, v. 16, n. 788, p. 1, doi. 10.1126/scisignal.add6364
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- Article
Progressive NKCC1-Dependent Neuronal Chloride Accumulation during Neonatal Seizures.
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- Journal of Neuroscience, 2010, v. 30, n. 35, p. 11745, doi. 10.1523/JNEUROSCI.1769-10.2010
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- Publication type:
- Article
Role of NKCC1 and KCC2 in the development of chronic neuropathic pain following spinal cord injury.
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- Annals of the New York Academy of Sciences, 2010, v. 1198, n. 1, p. 168, doi. 10.1111/j.1749-6632.2010.05462.x
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- Publication type:
- Article
Molecular Diagnostic Yield of Exome Sequencing in Patients With Congenital Hydrocephalus: A Systematic Review and Meta-Analysis.
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- JAMA Network Open, 2023, v. 6, n. 11, p. e2343384, doi. 10.1001/jamanetworkopen.2023.43384
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- Publication type:
- Article
Visualizing flow in an intact CSF network using optical coherence tomography: implications for human congenital hydrocephalus.
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- Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-019-42549-4
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- Publication type:
- Article
GABA<sub>A</sub> receptor dependent synaptic inhibition rapidly tunes KCC2 activity via the Cl<sup>-</sup>-sensitive WNK1 kinase.
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- Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-01749-0
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- Article
Glioblastoma mimicking an arteriovenous malformation.
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- Frontiers in Neurology, 2013, v. 4, p. 1, doi. 10.3389/fneur.2013.00144
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- Publication type:
- Article
Limitations of current GABA agonists in neonatal seizures: toward GABA modulation via the targeting of neuronal Cl<sup>-</sup> transport.
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- Frontiers in Neurology, 2013, v. 4, p. 1, doi. 10.3389/fneur.2013.00078
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- Publication type:
- Article
Impaired regulation of KCC2 phosphorylation leads to neuronal network dysfunction and neurodevelopmental pathology.
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- Science Signaling, 2019, v. 12, n. 603, p. 1, doi. 10.1126/scisignal.aay0300
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- Publication type:
- Article
Developmentally regulated KCC2 phosphorylation is essential for dynamic GABA-mediated inhibition and survival.
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- Science Signaling, 2019, v. 12, n. 603, p. 1, doi. 10.1126/scisignal.aaw9315
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- Publication type:
- Article
Molecular Genetics and Complex Inheritance of Congenital Heart Disease.
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- Genes, 2021, v. 12, n. 7, p. 1020, doi. 10.3390/genes12071020
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- Publication type:
- Article
Concurrent impact of de novo mutations on cranial and cortical development in nonsyndromic craniosynostosis.
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- Journal of Neurosurgery: Pediatrics, 2024, v. 33, n. 1, p. 59, doi. 10.3171/2023.8.PEDS23155
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- Publication type:
- Article
Increasing precision in the management of pediatric neurosurgical cerebrovascular diseases with molecular genetics.
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- Journal of Neurosurgery: Pediatrics, 2023, v. 31, n. 3, p. 228, doi. 10.3171/2022.12.PEDS22332
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- Publication type:
- Article
Genomic approaches to improve the clinical diagnosis and management of patients with congenital hydrocephalus.
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- Journal of Neurosurgery: Pediatrics, 2022, v. 29, n. 2, p. 168, doi. 10.3171/2021.8.PEDS21368
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- Publication type:
- Article
Recessive Inheritance of Congenital Hydrocephalus With Other Structural Brain Abnormalities Caused by Compound Heterozygous Mutations in ATP1A3.
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- Frontiers in Cellular Neuroscience, 2019, p. 1, doi. 10.3389/fncel.2019.00425
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- Article
Wnk4 controls blood pressure and potassium homeostasis via regulation of mass and activity of the distal convoluted tubule.
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- Nature Genetics, 2006, v. 38, n. 10, p. 1124, doi. 10.1038/ng1877
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- Article
WNK4 regulates the balance between renal NaCl reabsorption and K<sup>+</sup> secretion.
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- Nature Genetics, 2003, v. 35, n. 4, p. 372, doi. 10.1038/ng1271
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- Article
Cerebrospinal fluid hypersecretion in pediatric hydrocephalus.
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- Neurosurgical Focus, 2016, v. 41, n. 5, p. 1, doi. 10.3171/2016.8.FOCUS16278
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- Publication type:
- Article
The WNK-regulated SPAK/OSR1 kinases directly phosphorylate and inhibit the K<sup>+</sup> -Cl<sup>-</sup> co-transporters.
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- Biochemical Journal, 2014, v. 458, n. 3, p. 559, doi. 10.1042/BJ20131478
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- Article
Protein kinase D1 variant associated with human epilepsy and peripheral nerve hypermyelination.
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- Clinical Genetics, 2021, v. 100, n. 2, p. 176, doi. 10.1111/cge.13973
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- Article
Novel EWSR1‐VGLL1 fusion in a pediatric neuroepithelial neoplasm.
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- Clinical Genetics, 2020, v. 97, n. 5, p. 791, doi. 10.1111/cge.13703
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- Article
Regulatory domain or CpG site variation in SLC12A5, encoding the chloride transporter KCC2, in human autism and schizophrenia.
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- Frontiers in Cellular Neuroscience, 2015, v. 9, p. 1, doi. 10.3389/fncel.2015.00386
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- Publication type:
- Article
Regulated phosphorylation of the K-Cl cotransporter KCC3 is a molecular switch of intracellular potassium content and cell volume homeostasis.
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- Frontiers in Cellular Neuroscience, 2015, v. 9, p. 1, doi. 10.3389/fncel.2015.00255
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- Publication type:
- Article
WNK3, a kinase related to genes mutated in hereditary hypertension with hyperkalaemia, regulates the K<sup>+</sup> channel ROMK1 (Kir1.1).
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- Journal of Physiology, 2006, v. 571, n. 2, p. 275, doi. 10.1113/jphysiol.2005.102202
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- Article
Author Correction: Visualizing flow in an intact CSF network using optical coherence tomography: implications for human congenital hydrocephalus.
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- 2020
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- Correction Notice
Utility of cortical tissue analysis in normal pressure hydrocephalus.
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- Cerebral Cortex, 2024, v. 34, n. 2, p. 1, doi. 10.1093/cercor/bhae001
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- Article
The "microcephalic hydrocephalus" paradox as a paradigm of altered neural stem cell biology.
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- Cerebral Cortex, 2024, v. 34, n. 1, p. 1, doi. 10.1093/cercor/bhad432
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- Article
Cases of familial idiopathic normal pressure hydrocephalus implicate genetic factors in disease pathogenesis.
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- Cerebral Cortex, 2023, v. 33, n. 23, p. 11400, doi. 10.1093/cercor/bhad374
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- Article
"Floppy brain" in congenital hydrocephalus.
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- Cerebral Cortex, 2023, v. 33, n. 15, p. 9339, doi. 10.1093/cercor/bhad206
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- Article
A neural stem cell paradigm of pediatric hydrocephalus.
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- Cerebral Cortex, 2023, v. 33, n. 8, p. 4262, doi. 10.1093/cercor/bhac341
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- Publication type:
- Article
The WNK-SPAK/OSR1 Kinases and the Cation-Chloride Cotransporters as Therapeutic Targets for Neurological Diseases.
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- Aging & Disease, 2019, v. 10, n. 3, p. 626, doi. 10.14336/AD.2018.0928
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- Publication type:
- Article
Bumetanide Enhances Phenobarbital Efficacy in a Rat Model of Hypoxic Neonatal Seizures.
- Published in:
- PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0057148
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- Publication type:
- Article
Craniectomy for Malignant Cerebral Infarction: Prevalence and Outcomes in US Hospitals.
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- PLoS ONE, 2011, v. 6, n. 12, p. 1, doi. 10.1371/journal.pone.0029193
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- Publication type:
- Article
Interfacility Helicopter Ambulance Transport of Neurosurgical Patients: Observations, Utilization, and Outcomes from a Quaternary Level Care Hospital.
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- PLoS ONE, 2011, v. 6, n. 10, p. 1, doi. 10.1371/journal.pone.0026216
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- Publication type:
- Article
Response to the BRAF/MEK inhibitors dabrafenib/trametinib in an adolescent with a BRAF V600E mutated anaplastic ganglioglioma intolerant to vemurafenib.
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- 2018
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- Publication type:
- journal article
WNK-Cab39-NKCC1 signaling increases the susceptibility to ischemic brain damage in hypertensive rats.
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- Journal of Cerebral Blood Flow & Metabolism, 2017, v. 37, n. 8, p. 2780, doi. 10.1177/0271678X16675368
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- Publication type:
- Article
Deletion of the WNK3-SPAK kinase complex in mice improves radiographic and clinical outcomes in malignant cerebral edema after ischemic stroke.
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- Journal of Cerebral Blood Flow & Metabolism, 2017, v. 37, n. 2, p. 550, doi. 10.1177/0271678X16631561
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- Publication type:
- Article
GemC1 is a critical switch for neural stem cell generation in the postnatal brain.
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- Glia, 2019, v. 67, n. 12, p. 2360, doi. 10.1002/glia.23690
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- Article
GABAergic disinhibition and impaired KCC2 cotransporter activity underlie tumor-associated epilepsy.
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- Glia, 2015, v. 63, n. 1, p. 23, doi. 10.1002/glia.22730
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- Publication type:
- Article
Functional kinomics establishes a critical node of volume-sensitive cation-Cl<sup>−</sup> cotransporter regulation in the mammalian brain.
- Published in:
- Scientific Reports, 2016, p. 35986, doi. 10.1038/srep35986
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- Publication type:
- Article