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21. Design and implementation of electronic health record common data elements for pediatric epilepsy: Foundations for a learning health care system. (24th December 2020)

22. DNM1 encephalopathy: A new disease of vesicle fission. (25th July 2017)

23. Epilepsy Course and Developmental Trajectories in STXBP1-DEE. (31st May 2022)

24. Epilepsy Course and Developmental Trajectories in STXBP1-DEE. (31st May 2022)

26. Exon‐disrupting deletions of NRXN1 in idiopathic generalized epilepsy. (7th January 2013)

27. Genetic literacy series: Primer part 2—Paradigm shifts in epilepsy genetics. (9th May 2018)

28. Genome-wide rare copy number variation screening in ulcerative colitis identifies potential susceptibility loci. Issue 1 (December 2016)

30. Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsies. Issue 9 (29th July 2017)