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31. Rare variants in γ‐aminobutyric acid type A receptor genes in rolandic epilepsy and related syndromes. Issue 6 (28th March 2015)

32. SCN1A variants from bench to bedside—improved clinical prediction from functional characterization. Issue 2 (28th November 2019)

33. Shared genetic basis between genetic generalized epilepsy and background electroencephalographic oscillations. (18th May 2021)

34. Simultaneous impairment of neuronal and metabolic function of mutated gephyrin in a patient with epileptic encephalopathy. Issue 12 (1st December 2017)

35. Simultaneous impairment of neuronal and metabolic function of mutated gephyrin in a patient with epileptic encephalopathy. Issue 12 (27th November 2015)

38. Spectrum of neurodevelopmental disease associated with the GNAO1 guanosine triphosphate–binding region. (25th January 2019)

39. Spectrum of Phenotypic, Genetic, and Functional Characteristics in Patients With Epilepsy With KCNC2 Pathogenic Variants. (17th May 2022)

40. Spectrum of Phenotypic, Genetic, and Functional Characteristics in Patients With Epilepsy With KCNC2 Pathogenic Variants. (17th May 2022)