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497 results

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Page 1
Expression of SMARCB1 (INI1) mutations in familial schwannomatosis.
Smith MJ, Walker JA, Shen Y, Stemmer-Rachamimov A, Gusella JF, Plotkin SR. Smith MJ, et al. Among authors: walker ja. Hum Mol Genet. 2012 Dec 15;21(24):5239-45. doi: 10.1093/hmg/dds370. Epub 2012 Sep 4. Hum Mol Genet. 2012. PMID: 22949514 Free PMC article.
Plasma S100β is not a useful biomarker for tumor burden in neurofibromatosis.
Smith MJ, Esparza S, Merker VL, Muzikansky A, Bredella MA, Harris GJ, Kassarjian A, Cai W, Walker JA, Mautner VF, Plotkin SR. Smith MJ, et al. Among authors: walker ja. Clin Biochem. 2013 May;46(7-8):698-700. doi: 10.1016/j.clinbiochem.2012.12.007. Epub 2012 Dec 19. Clin Biochem. 2013. PMID: 23261835
Pain correlates with germline mutation in schwannomatosis.
Jordan JT, Smith MJ, Walker JA, Erdin S, Talkowski ME, Merker VL, Ramesh V, Cai W, Harris GJ, Bredella MA, Seijo M, Suuberg A, Gusella JF, Plotkin SR. Jordan JT, et al. Among authors: walker ja. Medicine (Baltimore). 2018 Feb;97(5):e9717. doi: 10.1097/MD.0000000000009717. Medicine (Baltimore). 2018. PMID: 29384852 Free PMC article.
Emerging therapeutic targets for neurofibromatosis type 1.
Walker JA, Upadhyaya M. Walker JA, et al. Expert Opin Ther Targets. 2018 May;22(5):419-437. doi: 10.1080/14728222.2018.1465931. Epub 2018 May 7. Expert Opin Ther Targets. 2018. PMID: 29667529 Free PMC article. Review.
497 results