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1. Surgical management of Rathke cleft cysts in pediatric patients: a single institution experience.

2. Special Considerations in Pediatric Endoscopic Skull Base Surgery.

4. Sex ratio and age of onset in AQP4 antibody-associated NMOSD: a review and meta-analysis

5. Identification of the DNA methylation signature of Mowat-Wilson syndrome

6. The detection of a strong episignature for Chung–Jansen syndrome, partially overlapping with Börjeson–Forssman–Lehmann and White–Kernohan syndromes

8. Intra-tumoral T cells in pediatric brain tumors display clonal expansion and effector properties

10. Frequency and predictors of concurrent complications in multi-suture release for syndromic craniosynostosis.

11. Circular extrachromosomal DNA promotes tumor heterogeneity in high-risk medulloblastoma

12. Artificial cranial deformation in Tiwanaku, Bolivia.

16. Histology of the Porous Oculomotorius: Relevance to Anterior Skull Base Approaches

17. Challenging, giant occipital encephalocele in a pediatric saipanese male.

25. Magnetic resonance imaging-guided stereotactic laser ablation therapy for the treatment of pediatric epilepsy: a retrospective multiinstitutional study.

27. Making inroads to precision medicine for the treatment of autoimmune diseases: Harnessing genomic studies to better diagnose and treat complex disorders

28. 3D genome mapping identifies subgroup-specific chromosome conformations and tumor-dependency genes in ependymoma

30. Association between B-cell depletion and attack risk in neuromyelitis optica spectrum disorder: An exploratory analysis from N-MOmentum, a double-blind, randomised, placebo-controlled, multicentre phase 2/3 trial

35. The role of methylation profiling in histologically diagnosed neurocytoma: a case series

36. Lack of association between classical HLA genes and asymptomatic SARS-CoV-2 infection

37. Menke-Hennekam syndrome; delineation of domain-specific subtypes with distinct clinical and DNA methylation profiles

38. MSL2 variants lead to a neurodevelopmental syndrome with lack of coordination, epilepsy, specific dysmorphisms, and a distinct episignature

39. The Path to a Match for Interventional Cardiology Fellowship: A Major SCAI Initiative

42. Diagnostic utility and reporting recommendations for clinical DNA methylation episignature testing in genetically undiagnosed rare diseases

44. Scalable Reverse Image Search Engine for NASAWorldview

46. Maturation of the internal auditory canal and posterior petrous bone with relevance to lateral and posterolateral skull base approaches.

48. Optimizing the location of vaccination sites to stop a zoonotic epidemic

50. Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability

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