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193 results on '"Hendson, Glenda"'

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1. Comparative RNA-Sequencing Analysis Benefits a Pediatric Patient With Relapsed Cancer

6. Pathogenetics of alveolar capillary dysplasia with misalignment of pulmonary veins

7. Low-grade diffusely infiltrative tumour (LGDIT), SMARCB1-mutant : A clinical and histopathological distinct entity showing epigenetic similarity with ATRT-MYC

9. The role of resection alone in select children with intracranial ependymoma: the Canadian Pediatric Brain Tumour Consortium experience

10. ATRT-07. Low-grade diffusely infiltrative tumor, SMARCB1-mutant: a clinical and histopathological distinct entity showing epigenetic similarity with ATRT-MYC

11. Low‐grade diffusely infiltrative tumour (LGDIT), SMARCB1‐mutant: A clinical and histopathological distinct entity showing epigenetic similarity with ATRT‐MYC

12. Loss-of-function mutations in SCN4A cause severe foetal hypokinesia or ‘classical’ congenital myopathy

13. Lethal respiratory course and additional features expand the phenotypic spectrum of PIEZO2‐related distal arthrogryposis type 5.

15. EZH2 Expression Is a Prognostic Factor in Childhood Intracranial Ependymoma: A Canadian Pediatric Brain Tumor Consortium Study

21. Hypomorphic temperature-sensitive alleles of NSDHL cause CK syndrome

24. Novel findings and expansion of phenotype in a mosaicRASopathycaused by somaticKRASvariants

33. Epidural Spinal Tumors

34. An infant with congenital respiratory insufficiency and diaphragmatic paralysis: A novel BICD2 phenotype?

38. Novel findings and expansion of phenotype in a mosaic RASopathy caused by somatic KRAS variants.

39. Reduced elastogenesis: a clue to the arteriosclerosis and emphysematous changes in Schimke immuno-osseous dysplasia?

42. Increased Wnt and Notch signaling: a clue to the renal disease in Schimke immuno-osseous dysplasia?

43. Reduced elastogenesis: a clue to the arteriosclerosis and emphysematous changes in Schimke immuno-osseous dysplasia?

44. Loss-of-function mutations inSCN4Acause severe foetal hypokinesia or ‘classical’ congenital myopathy

45. MG-115 Compound heterozygous SCN4A mutation underlies severe congenital hypotonia and biophysical alteration in the encoded voltage-gated NAV1.4 sodium channel

48. Transcriptional and posttranscriptional mechanisms contribute to the dysregulation of elastogenesis in Schimke immuno-osseous dysplasia

49. Cerebellar Vermian Atrophy after Neonatal Hypoxic-Ischemic Encephalopathy

50. The role of resection alone in select children with intracranial ependymoma: the Canadian Pediatric Brain Tumour Consortium experience

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