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NRXN1 deletion syndrome; phenotypic and penetrance data from 34 families.
Al Shehhi M, Forman EB, Fitzgerald JE, McInerney V, Krawczyk J, Shen S, Betts DR, Ardle LM, Gorman KM, King MD, Green A, Gallagher L, Lynch SA. Al Shehhi M, et al. Among authors: forman eb. Eur J Med Genet. 2019 Mar;62(3):204-209. doi: 10.1016/j.ejmg.2018.07.015. Epub 2018 Jul 18. Eur J Med Genet. 2019. PMID: 30031152
Cost of exome sequencing in epileptic encephalopathy: is it 'worth it'?
Forman EB, Gorman KM, Conroy J, Arthur N, Grant C, Ennis S, Allen NM, Lynch SA, King MD. Forman EB, et al. Arch Dis Child. 2018 Mar;103(3):304. doi: 10.1136/archdischild-2017-313240. Epub 2017 Sep 22. Arch Dis Child. 2018. PMID: 28939639 No abstract available.
SCN1A Variant and Cannabidiol Use.
Reynolds C, Finnegan R, Forman E, King MD. Reynolds C, et al. Ir Med J. 2018 Feb 9;111(2):702. Ir Med J. 2018. PMID: 29952450 No abstract available.
"No-No" Head Tremor-A Nod to the Diagnosis.
Terry C, Forman EB, Gorman KM, King MD. Terry C, et al. Among authors: forman eb. Pediatr Neurol. 2019 Nov;100:104. doi: 10.1016/j.pediatrneurol.2019.03.007. Epub 2019 Mar 19. Pediatr Neurol. 2019. PMID: 31003879 No abstract available.
23 results