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Ingo Helbig · @IngoHelbig. ·. Feb 28, Phenotypes are like water – Rare Disease Day | Beyond the Ion Channel http://epilepsygenetics.net Ingo Helbig · @IngoHelbig. ·. Feb 28, Phenotypes are like water – Rare Disease Day | Beyond the Ion Channel http://epilepsygenetics.net

Ingo Helbig | Beyond the Ion Channel

epilepsygenetics.net

Posted on July 8, by Ingo Helbig Beyond GRIN2A . The childhood epilepsies traditionally referred to as Benign Rolandic Epilepsy (BRE) or benign epilepsy with centro-temporal spikes (BECTS) have had various names in the past, which reflects somewhat the difficulties of fully putting this group of seizure disorders into clear categories.

Ingo Helbig (Kiel) | Beyond the Ion Channel

epilepsygenetics.net

Posted on January 13, by Ingo Helbig (Kiel) ... But we also need to reconsider the name of this blog – we are far from being beyond the ion channel.

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Ingo Helbig · @IngoHelbig. The history of epilepsy genetics | Beyond the Ion Channel http://epilepsygenetics.net the-history-of ... Ingo Helbig · @IngoHelbig. The history of epilepsy genetics | Beyond the Ion Channel http://epilepsygenetics.net the-history-of ...

Ingo Helbig | Beyond the Ion Channel | Page 5

euroepinomics.wordpress.com

Read all of the posts by Ingo Helbig on Beyond the Ion Channel

How to deal with scientific disappointment | Beyond the Ion Channel

euroepinomics.wordpress.com

Difficult times. The last two weeks were hard for me scientifically. In addition to having two papers rejected within a week, I learned that a major grant...

How to become a pediatric neurologist | Beyond the Ion Channel

euroepinomics.wordpress.com

Milestones. Today I passed my board exam for pediatric neurology or neuropediatrics, as we call it in Germany. Even though I am usually not big on celebrating...

Alle Infos zum Namen "Ingo Helbig"

Beyond the Ion Channel | The ILAE Genetics Commission Blog

epilepsygenetics.net

Posted on June 17, by Ingo Helbig. The missing ion channel. A little more than two years ago, we wrote about our discovery of SCN3A as a novel disease gene in epileptic encephalopathies. At the time, SCN3A was the missing ion channel, the only brain-expressed voltage gated sodium channel that did not have a clear gene-disease relationship.