237 results on '"Duy Phan Q."'
Search Results
2. The genetic basis of hydrocephalus: genes, pathways, mechanisms, and global impact
3. Fragile X syndrome: Lessons learned from the most translated neurodevelopmental disorder in clinical trials
4. Hydrocephalus
5. Mutation of key signaling regulators of cerebrovascular development in vein of Galen malformations
6. Multiomic analyses implicate a neurodevelopmental program in the pathogenesis of cerebral arachnoid cysts
7. TRIM71 mutations cause a neurodevelopmental syndrome featuring ventriculomegaly and hydrocephalus
8. Cellular recovery after prolonged warm ischaemia of the whole body
9. Impaired neurogenesis alters brain biomechanics in a neuroprogenitor-based genetic subtype of congenital hydrocephalus
10. Biomechanical instability of the brain–CSF interface in hydrocephalus.
11. MRI in Spine Trauma
12. Inflammatory hydrocephalus
13. Genomics of human congenital hydrocephalus
14. Pathogenic variants in autism gene KATNAL2 cause hydrocephalus and disrupt neuronal connectivity by impairing ciliary microtubule dynamics.
15. Worse overall health status negatively impacts satisfaction with breast reconstruction
16. Derivation and validation of genome-wide polygenic score for urinary tract stone diagnosis
17. Exome Sequencing Implicates Impaired GABA Signaling and Neuronal Ion Transport in Trigeminal Neuralgia
18. Preresidency Publication Productivity of U.S. Neurosurgery Interns
19. A novel SMARCC1 BAFopathy implicates neural progenitor epigenetic dysregulation in human hydrocephalus
20. Retinal innervation tunes circuits that drive nonphotic entrainment to food
21. Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalus
22. Inflammation in acquired hydrocephalus: pathogenic mechanisms and therapeutic targets
23. Trim71/lin-41 Links an Ancient miRNA Pathway to Human Congenital Hydrocephalus
24. Timing and prevalence of revision and removal surgeries after spinal cord stimulator implantation
25. A novel SMARCC1 BAFopathy implicates neural progenitor epigenetic dysregulation in human hydrocephalus.
26. The “microcephalic hydrocephalus” paradox as a paradigm of altered neural stem cell biology
27. Spine Surgery HCAHPS Patient Satisfaction Survey Results Inversely Correlate with Survey Response Time
28. Cases of familial idiopathic normal pressure hydrocephalus implicate genetic factors in disease pathogenesis
29. Concurrent impact of de novo mutations on cranial and cortical development in nonsyndromic craniosynostosis
30. Utility of cortical tissue analysis in normal pressure hydrocephalus.
31. Concurrent impact of de novo mutations on cranial and cortical development in nonsyndromic craniosynostosis.
32. The "microcephalic hydrocephalus" paradox as a paradigm of altered neural stem cell biology.
33. Genetic dysregulation of an endothelial Ras signaling network in vein of Galen malformations
34. Dual impact of PTEN mutation on CSF dynamics and cortical networks via the dysregulation of neural precursors and their interneuron descendants
35. The choroid plexus links innate immunity to CSF dysregulation in hydrocephalus
36. Rethinking the cilia hypothesis of hydrocephalus
37. A neural stem cell paradigm of pediatric hydrocephalus
38. Rare pathogenic variants in WNK3 cause X-linked intellectual disability
39. "Floppy brain" in congenital hydrocephalus.
40. spARC recovers human glioma spatial signaling networks with graph filtering
41. Familial and syndromic forms of arachnoid cyst implicate genetic factors in disease pathogenesis
42. Molecular genetics of human developmental neurocranial anomalies: towards “precision surgery”
43. A neural stem cell paradigm of pediatric hydrocephalus.
44. Angiographic Pulse Wave Coherence in the Human Brain
45. Brain ventricles as windows into brain development and disease
46. PTEN mutations in autism spectrum disorder and congenital hydrocephalus: developmental pleiotropy and therapeutic targets
47. Opioid use and spinal cord stimulation therapy: The long game
48. Motoneuron development influences dorsal root ganglia survival and Schwann cell development in a vertebrate model of spinal muscular atrophy
49. DIAPH1 Variants in Non–East Asian Patients With Sporadic Moyamoya Disease
50. Spinal cord stimulation and psychotropic medication use: Missing piece to the puzzle?
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