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52. Primer Part 1—The building blocks of epilepsy genetics. (25th May 2016)

53. PRRT2 mutations: exploring the phenotypical boundaries. Issue 4 (7th October 2013)

54. PURA-Related Developmental and Epileptic Encephalopathy: Phenotypic and Genotypic Spectrum. (15th December 2021)

55. PURA-Related Developmental and Epileptic Encephalopathy: Phenotypic and Genotypic Spectrum. (December 2021)

56. Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study. Issue 8 (August 2018)

57. Rare Noncoding Mutations Extend the Mutational Spectrum in the PGAP3 Subtype of Hyperphosphatasia with Mental Retardation Syndrome. Issue 8 (19th May 2016)

58. RARS1‐related hypomyelinating leukodystrophy: Expanding the spectrum. Issue 1 (8th December 2019)

59. Recessive loss-of-function mutations in AP4S1 cause mild fever-sensitive seizures, developmental delay and spastic paraplegia through loss of AP-4 complex assembly. (30th December 2014)

60. Recessive mutations in SLC35A3 cause early onset epileptic encephalopathy with skeletal defects. Issue 4 (22nd March 2017)