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6 results
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Prefibrotic Myelofibrosis Presenting with Multiple Cerebral Embolic Infarcts and the Rare MPL W515S Mutation.
Case Rep Hematol. 2020 Jun 19;2020:8375986. doi: 10.1155/2020/8375986. eCollection 2020.
Case Rep Hematol. 2020.
PMID: 32637179
Free PMC article.
MPL exon 10 mutations in Irish patients with a suspected myeloproliferative neoplasm.
Lee Tokar L, Kearney L, Langabeer SE.
Lee Tokar L, et al.
EXCLI J. 2021 Feb 1;20:197-198. doi: 10.17179/excli2021-3454. eCollection 2021.
EXCLI J. 2021.
PMID: 33628158
Free PMC article.
No abstract available.
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CALR Mutation Underlying Silent Stroke.
Faryal R, Lee Tokar L, Langabeer SE, Krawczyk J.
Faryal R, et al. Among authors: lee tokar l.
TH Open. 2021 Jun 1;5(2):e174-e175. doi: 10.1055/s-0041-1728674. eCollection 2021 Apr.
TH Open. 2021.
PMID: 34104855
Free PMC article.
No abstract available.
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Myeloproliferative neoplasms with a low (<5%) CALR mutation allele burden.
Lee Tokar L, Crotty G, O'Keeffe D, Langabeer SE.
Lee Tokar L, et al.
Blood Cells Mol Dis. 2021 Sep;90:102593. doi: 10.1016/j.bcmd.2021.102593. Epub 2021 Jun 29.
Blood Cells Mol Dis. 2021.
PMID: 34217938
No abstract available.
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Repeat JAK2 V617F testing in patients with suspected essential thrombocythaemia.
Kearney L, Lee Tokar L, Flynn C, Mykytiv V, Murphy K, Langabeer SE.
Kearney L, et al. Among authors: lee tokar l.
J Clin Pathol. 2020 Nov;73(11):772. doi: 10.1136/jclinpath-2020-206778. Epub 2020 Jul 9.
J Clin Pathol. 2020.
PMID: 32646925
Review.
No abstract available.
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Detection of JAK2 Exon 12 Mutations in Suspected Polycythemia Vera by Next-Generation Sequencing.
Lee-Tokar L, Kearney L, Langabeer SE.
Lee-Tokar L, et al.
Clin Lab. 2022 Jan 1;68(1). doi: 10.7754/Clin.Lab.2021.210510.
Clin Lab. 2022.
PMID: 35023693
No abstract available.
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