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Clinical impact of a targeted next-generation sequencing gene panel for autoinflammation and vasculitis.
PLoS One. 2017 Jul 27;12(7):e0181874. doi: 10.1371/journal.pone.0181874. eCollection 2017.
PLoS One. 2017.
PMID: 28750028
Free PMC article.
Moyamoya-like cerebrovascular disease in a child with a novel mutation in myosin heavy chain 11.
Keylock A, Hong Y, Saunders D, Omoyinmi E, Mulhern C, Roebuck D, Brogan P, Ganesan V, Eleftheriou D.
Keylock A, et al.
Neurology. 2018 Jan 16;90(3):136-138. doi: 10.1212/WNL.0000000000004828. Epub 2017 Dec 20.
Neurology. 2018.
PMID: 29263223
Free PMC article.
No abstract available.
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Cerebral arteriopathy associated with heterozygous variants in the casitas B-lineage lymphoma gene.
Hong Y, Keylock A, Jensen B, Jacques TS, Ogunbiyi O, Omoyinmi E, Saunders D, Mallick AA, Tooley M, Newbury-Ecob R, Rankin J, Williams HJ, Ganesan V, Brogan PA, Eleftheriou D.
Hong Y, et al. Among authors: keylock a.
Neurol Genet. 2020 Jun 10;6(4):e448. doi: 10.1212/NXG.0000000000000448. eCollection 2020 Aug.
Neurol Genet. 2020.
PMID: 32637631
Free PMC article.
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Stroke in childhood neurofibromatosis type 2.
Kirkham FJ, Keylock A, Saunders DE.
Kirkham FJ, et al. Among authors: keylock a.
Dev Med Child Neurol. 2018 Dec;60(12):1199-1200. doi: 10.1111/dmcn.13965. Epub 2018 Jul 2.
Dev Med Child Neurol. 2018.
PMID: 29963697
Free article.
No abstract available.
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