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102 results on '"Phan, Q"'

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1. Hydrocephalus

2. TRIM71 mutations cause a neurodevelopmental syndrome featuring ventriculomegaly and hydrocephalus

4. The genetic basis of hydrocephalus: genes, pathways, mechanisms, and global impact

5. A novel SMARCC1 BAFopathy implicates neural progenitor epigenetic dysregulation in human hydrocephalus

7. Mutation of key signaling regulators of cerebrovascular development in vein of Galen malformations

8. Abstract 16558: Revascularization in Patients With Ischemic Cardiomyopathy and Viability: A Meta-Analysis of Randomized Controlled Trials

9. Cases of familial idiopathic normal pressure hydrocephalus implicate genetic factors in disease pathogenesis

10. Concurrent impact of de novo mutations on cranial and cortical development in nonsyndromic craniosynostosis

11. MRI in Spine Trauma

12. Genetic dysregulation of an endothelial Ras signaling network in vein of Galen malformations

13. Dual impact of PTEN mutation on CSF dynamics and cortical networks via the dysregulation of neural precursors and their interneuron descendants

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

15. The choroid plexus links innate immunity to CSF dysregulation in hydrocephalus

17. A neural stem cell paradigm of pediatric hydrocephalus

18. Rare pathogenic variants in WNK3 cause X-linked intellectual disability

19. spARC recovers human glioma spatial signaling networks with graph filtering

20. Cellular recovery after prolonged warm ischaemia of the whole body

23. Angiographic Pulse Wave Coherence in the Human Brain

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

26. PTEN mutations in autism spectrum disorder and congenital hydrocephalus: developmental pleiotropy and therapeutic targets

27. Use of Slaughterhouses as Sentinel Points for Genomic Surveillance of Foot-and-Mouth Disease Virus in Southern Vietnam

29. DIAPH1 Variants in Non–East Asian Patients With Sporadic Moyamoya Disease

30. Genomics of human congenital hydrocephalus

31. Inflammatory hydrocephalus

37. Derivation and validation of genome-wide polygenic score for urinary tract stone diagnosis

38. Self-reported health without clinically measurable benefits among adult users of multivitamin and multimineral supplements: a cross-sectional study

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

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

46. Preresidency Publication Productivity of U.S. Neurosurgery Interns

48. Inflammation in acquired hydrocephalus: pathogenic mechanisms and therapeutic targets

49. Genomic alterations underlying spinal metastases in pediatric H3K27M-mutant pineal parenchymal tumor of intermediate differentiation: case report

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