
Ethan Goldberg
@go3than
Pediatric neurologist; Neurogeneticist; Neurobiologist; Fantasy Baseball player; Amateur chess enthusiast; Dad.
ID: 1430282803
http://www.goldbergneurolab.com 15-05-2013 11:25:39
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496 Followers
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Today we’re celebrating the groundbreaking of the latest addition to Children's Hospital’s research campus, the Schuylkill Avenue Research Building.




Thanks to NINDSfunding for support of this preclinical work leading to a candidate therapy for EPM7. This collaboration was led by postdoc Jade Feng with Autifony Therapeutics Manuel Covarrubias Naiara Akizu. We will continue to work to improve the lives of patients with rare disease.


Postdoctoral Fellowship for Academic Diversity at The Children's Hospital of Philadelphia: - $65K salary in Yr 1, increasing in $2K yearly increments - Annual travel ($2K) allowance and supplies ($4K) - Relocation bonus ($5K) - Supervised research training research.chop.edu/services/postd…


Another fun collaboration w/ Christopher Currin, PhD 🌍 🇿🇦 & Tim Vogels plus @DelemotteLab and Manuel Covarrubias: Jerome Clatot et al. A structurally precise mechanism links an epilepsy-associated KCNC2 potassium channel mutation to interneuron dysfunction | PNAS pnas.org/doi/10.1073/pn…






From postdoc Sophie Hill in a fun collaboration w/ EAP expert Brian Theyel supported by Dravet Syndrome Foundation : Attenuated Ectopic Action Potential firing in PV interneurons in a mouse model of Dravet Syndrome biorxiv.org/content/10.110… The function of EAPs remains under investigation...


Rising star @ZPRosenthal PGY-3 Resident Penn Psychiatry uses a novel mouse model of electroconvulsive therapy (ECT) and DCS/FD-DOS in humans to show that: ECT generates a hidden wave - CSD - after seizure biorxiv.org/content/10.110…

New collaboration with David R. Liu to pursue base editing in a Dravet syndrome model. Thanks to Dravet Syndrome Foundation for your leadership and vision and continued support of our work to improve the lives of patients with Dravet Syndrome. einpresswire.com/article/769708…

Rare variants in epilepsy- and autism-linked gene SCN2A are associated with malformation of cortical development, supporting role of NaV1.2 in early brain development: doi.org/10.1111/epi.18… Fun collaboration w/ Al George Nicola Specchio Renzo Guerrini Supported by NINDS


