979 results on '"Kahle, Kristopher T."'
Search Results
2. The genetic basis of hydrocephalus: genes, pathways, mechanisms, and global impact
3. Rare variants in ANO1, encoding a calcium-activated chloride channel, predispose to moyamoya disease.
4. Hydrocephalus
5. Mutation of key signaling regulators of cerebrovascular development in vein of Galen malformations
6. Epilepsy Surgery for Cognitive Improvement in Epileptic Encephalopathy
7. Multiomic analyses implicate a neurodevelopmental program in the pathogenesis of cerebral arachnoid cysts
8. Human genetics and molecular genomics of Chiari malformation type 1
9. The Efficacy of Endoscopic Third Ventriculostomy for Idiopathic Normal Pressure Hydrocephalus
10. De Novo Variants in RAB11B Cause Various Degrees of Global Developmental Delay and Intellectual Disability in Children
11. De novo mutations in the BMP signaling pathway in lambdoid craniosynostosis
12. De novo variants implicate chromatin modification, transcriptional regulation, and retinoic acid signaling in syndromic craniosynostosis
13. TRIM71 mutations cause a neurodevelopmental syndrome featuring ventriculomegaly and hydrocephalus
14. KCC2 drives chloride microdomain formation in dendritic blebbing
15. Impaired neurogenesis alters brain biomechanics in a neuroprogenitor-based genetic subtype of congenital hydrocephalus
16. Sustained glymphatic transport and impaired drainage to the nasal cavity observed in multiciliated cell ciliopathies with hydrocephalus
17. Role of SPAK–NKCC1 signaling cascade in the choroid plexus blood–CSF barrier damage after stroke
18. Biomechanical instability of the brain–CSF interface in hydrocephalus.
19. AXIN1 mutations in nonsyndromic craniosynostosis.
20. PPIL4 is essential for brain angiogenesis and implicated in intracranial aneurysms in humans
21. Algebraic Nexus of Fibonacci Forms and Two-Simplex Topology in Multicellular Morphogenesis
22. Inflammatory hydrocephalus
23. Genomics of human congenital hydrocephalus
24. Patient Risk Factors Associated With 30- and 90-Day Readmission After Ventriculoperitoneal Shunt Placement for Idiopathic Normal Pressure Hydrocephalus in Elderly Patients: A Nationwide Readmission Study
25. Impact of race on outcomes and healthcare utilization following spinal fusion for adolescent idiopathic scoliosis
26. The Effects of Pulmonary Risk Factors on Hospital Resource Use After Posterior Spinal Fusion for Adolescent Idiopathic Scoliosis Correction
27. Post-traumatic seizures following pediatric traumatic brain injury
28. Impact of Preoperative Anemia on Outcomes After Posterior Spinal Fusion for Adolescent Idiopathic Scoliosis
29. Exome Sequencing Implicates Impaired GABA Signaling and Neuronal Ion Transport in Trigeminal Neuralgia
30. Risk Factors for the Development of Post-Traumatic Hydrocephalus in Children
31. Risk Factors Portending Extended Length of Stay After Suboccipital Decompression for Adult Chiari I Malformation
32. Geographic Variation in Outcomes and Costs After Spinal Fusion for Adolescent Idiopathic Scoliosis
33. Glymphatic System Impairment in Alzheimer’s Disease and Idiopathic Normal Pressure Hydrocephalus
34. Stepwise Reconstruction of a Large, Self-Inflicted Calvarial Defect
35. De novo Variants Disrupt an LDB1-Regulated Transcriptional Network in Congenital Ventriculomegaly
36. Pre-operative headaches and obstructive hydrocephalus predict an extended length of stay following suboccipital decompression for pediatric Chiari I malformation
37. Neurosurgery elucidates somatic mutations
38. A novel SMARCC1 BAFopathy implicates neural progenitor epigenetic dysregulation in human hydrocephalus
39. Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalus
40. Inflammation in acquired hydrocephalus: pathogenic mechanisms and therapeutic targets
41. Trim71/lin-41 Links an Ancient miRNA Pathway to Human Congenital Hydrocephalus
42. EphrinB2-EphB4-RASA1 Signaling in Human Cerebrovascular Development and Disease
43. Transient Receptor Potential channels (TRP) in GtoPdb v.2023.3
44. Molecular Diagnostic Yield of Exome Sequencing in Patients With Congenital Hydrocephalus
45. The “microcephalic hydrocephalus” paradox as a paradigm of altered neural stem cell biology
46. Cases of familial idiopathic normal pressure hydrocephalus implicate genetic factors in disease pathogenesis
47. Concurrent impact of de novo mutations on cranial and cortical development in nonsyndromic craniosynostosis
48. Atlantoaxial instability associated with ALDH18A1 mutation
49. Persistent STAG2 mutation despite multimodal therapy in recurrent pediatric glioblastoma
50. WNK3 Kinase Is a Positive Regulator of NKCC2 and NCC, Renal $Cation-Cl^-$ Cotransporters Required for Normal Blood Pressure Homeostasis
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.