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Channelopathy as a SUDEP Biomarker in Dravet Syndrome Patient-Derived Cardiac Myocytes.
Frasier CR, Zhang H, Offord J, Dang LT, Auerbach DS, Shi H, Chen C, Goldman AM, Eckhardt LL, Bezzerides VJ, Parent JM, Isom LL. Frasier CR, et al. Among authors: goldman am. Stem Cell Reports. 2018 Sep 11;11(3):626-634. doi: 10.1016/j.stemcr.2018.07.012. Epub 2018 Aug 23. Stem Cell Reports. 2018. PMID: 30146492 Free PMC article.
Epilepsy Therapies Symposium | Do We Really "Outgrow" Seizures?
Ostendorf A, Waldman GJ, Jehi L, Ilyas M, Naritoku D, Goldman AM. Ostendorf A, et al. Among authors: goldman am. Epilepsy Curr. 2024 Dec 19:15357597241304501. doi: 10.1177/15357597241304501. Online ahead of print. Epilepsy Curr. 2024. PMID: 39712399 Free PMC article. Review.
Using high-frequency oscillations from brief intraoperative neural recordings to predict the seizure onset zone.
Fazli Besheli B, Sha Z, Gavvala JR, Karamursel S, Quach M, Swamy CP, Ayyoubi AH, Goldman AM, Curry DJ, Sheth SA, Darrow D, Miller KJ, Francis DJ, Worrell GA, Henry TR, Ince NF. Fazli Besheli B, et al. Among authors: goldman am. Commun Med (Lond). 2024 Nov 25;4(1):243. doi: 10.1038/s43856-024-00654-0. Commun Med (Lond). 2024. PMID: 39587325 Free PMC article.
Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections.
Jeffries L, Mis EK, McWalter K, Donkervoort S, Brodsky NN, Carpier JM, Ji W, Ionita C, Roy B, Morrow JS, Darbinyan A, Iyer K, Aul RB, Banka S, Chao KR, Cobbold L, Cohen S, Custodio HM, Drummond-Borg M, Elmslie F, Finanger E, Hainline BE, Helbig I, Hewson S, Hu Y, Jackson A, Josifova D, Konstantino M, Leach ME, Mak B, McCormick D, McGee E, Nelson S, Nguyen J, Nugent K, Ortega L, Goodkin HP, Roeder E, Roy S, Sapp K, Saade D, Sisodiya SM, Stals K, Towner S, Wilson W; Deciphering Developmental Disorders; Genomics England Research Consortium; Undiagnosed Disease Network; Khokha MK, Bönnemann CG, Lucas CL, Lakhani SA. Jeffries L, et al. Genet Med. 2024 Feb;26(2):101023. doi: 10.1016/j.gim.2023.101023. Epub 2023 Nov 7. Genet Med. 2024. PMID: 37947183
183 results