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Accumulated common variants in the broader fragile X gene family modulate autistic phenotypes.
Stepniak B, Kästner A, Poggi G, Mitjans M, Begemann M, Hartmann A, Van der Auwera S, Sananbenesi F, Krueger-Burg D, Matuszko G, Brosi C, Homuth G, Völzke H, Benseler F, Bagni C, Fischer U, Dityatev A, Grabe HJ, Rujescu D, Fischer A, Ehrenreich H. Stepniak B, et al. Among authors: poggi g. EMBO Mol Med. 2015 Dec;7(12):1565-79. doi: 10.15252/emmm.201505696. EMBO Mol Med. 2015. PMID: 26612855 Free PMC article.
Cortical network dysfunction caused by a subtle defect of myelination.
Poggi G, Boretius S, Möbius W, Moschny N, Baudewig J, Ruhwedel T, Hassouna I, Wieser GL, Werner HB, Goebbels S, Nave KA, Ehrenreich H. Poggi G, et al. Glia. 2016 Nov;64(11):2025-40. doi: 10.1002/glia.23039. Epub 2016 Jul 29. Glia. 2016. PMID: 27470661 Free PMC article.
The brain as immunoprecipitator of serum autoantibodies against N-Methyl-D-aspartate receptor subunit NR1.
Castillo-Gomez E, Kästner A, Steiner J, Schneider A, Hettling B, Poggi G, Ostehr K, Uhr M, Asif AR, Matzke M, Schmidt U, Pfander V, Hammer C, Schulz TF, Binder L, Stöcker W, Weber F, Ehrenreich H. Castillo-Gomez E, et al. Among authors: poggi g. Ann Neurol. 2016 Jan;79(1):144-51. doi: 10.1002/ana.24545. Epub 2015 Dec 2. Ann Neurol. 2016. PMID: 26505629
240 results