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An International Pediatric-Onset Opsoclonus-Myoclonus Ataxia Syndrome Registry and Clinical Research Network: Development, Progress, and Vision.
Kerr LM, Ryan ME, Lim M, Hearn S, Klein A, Deiva K, Hopkins SE, Bacchus MK, Sokol EA, Waanders AJ, Mitchell WG, Khakoo Y, Lotze TE, Zhang B, Gorman MP. Kerr LM, et al. Among authors: hopkins se. Pediatr Neurol. 2023 Nov;148:145-147. doi: 10.1016/j.pediatrneurol.2023.05.006. Epub 2023 May 16. Pediatr Neurol. 2023. PMID: 37716108 No abstract available.
Neurologic challenges in 22q11.2 deletion syndrome.
Hopkins SE, Chadehumbe M, Blaine Crowley T, Zackai EH, Bilaniuk LT, McDonald-McGinn DM. Hopkins SE, et al. Am J Med Genet A. 2018 Oct;176(10):2140-2145. doi: 10.1002/ajmg.a.38614. Epub 2018 Oct 26. Am J Med Genet A. 2018. PMID: 30365873 Review.
[No title available]
[No authors listed] [No authors listed] PMID: 39509184
90 results