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51. Epileptic spasms are a feature of DEPDC5 mTORopathy. (August 2015)

52. Evidence for a Dual-Pathway, 2-Hit Genetic Model for Focal Cortical Dysplasia and Epilepsy. (25th February 2022)

53. Evidence for a Dual-Pathway, 2-Hit Genetic Model for Focal Cortical Dysplasia and Epilepsy. (February 2022)

54. Exome sequencing for patients with developmental and epileptic encephalopathies in clinical practice. (14th June 2022)

55. Exome‐based analysis of cardiac arrhythmia, respiratory control, and epilepsy genes in sudden unexpected death in epilepsy. Issue 4 (2nd February 2016)

56. Expanding the genetic and phenotypic relevance of KCNB1 variants in developmental and epileptic encephalopathies: 27 new patients and overview of the literature. Issue 1 (4th October 2019)

57. Familial cortical dysplasia type IIA caused by a germline mutation in DEPDC5. (12th March 2015)

58. Familial neonatal seizures in 36 families: Clinical and genetic features correlate with outcome. (15th May 2015)

59. Familial neonatal seizures in 36 families: Clinical and genetic features correlate with outcome. (15th May 2015)

60. FBXO28 causes developmental and epileptic encephalopathy with profound intellectual disability. (6th December 2020)