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The clinical, genetic, and immune landscape of meningioma in patients with NF2-schwannomatosis.
Gregory GE, Islim AI, Hannan CJ, Jones AP, Hammerbeck-Ward C, Rutherford SA, Freeman SR, Lloyd S, Kalamarides M, Smith MJ, Couper K, McBain CA, Jenkinson MD, Brough D, King AT, Evans DG, Pathmanaban ON. Gregory GE, et al. Among authors: smith mj. Neurooncol Adv. 2023 Jun 3;5(Suppl 1):i94-i104. doi: 10.1093/noajnl/vdac127. eCollection 2023 May. Neurooncol Adv. 2023. PMID: 37287576 Free PMC article.
Cranial meningiomas in 411 neurofibromatosis type 2 (NF2) patients with proven gene mutations: clear positional effect of mutations, but absence of female severity effect on age at onset.
Smith MJ, Higgs JE, Bowers NL, Halliday D, Paterson J, Gillespie J, Huson SM, Freeman SR, Lloyd S, Rutherford SA, King AT, Wallace AJ, Ramsden RT, Evans DG. Smith MJ, et al. J Med Genet. 2011 Apr;48(4):261-5. doi: 10.1136/jmg.2010.085241. Epub 2011 Jan 28. J Med Genet. 2011. PMID: 21278391
Intronic splicing mutations in PTCH1 cause Gorlin syndrome.
Bholah Z, Smith MJ, Byers HJ, Miles EK, Evans DG, Newman WG. Bholah Z, et al. Among authors: smith mj. Fam Cancer. 2014 Sep;13(3):477-80. doi: 10.1007/s10689-014-9712-9. Fam Cancer. 2014. PMID: 24659465
1,744 results