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Screening for Fabry disease and Hereditary ATTR amyloidosis in idiopathic small-fiber and mixed neuropathy.
Samuelsson K, Radovic A, Press R, Auranen M, Ylikallio E, Tyynismaa H, KäRppä M, Veteläinen M, Peltola N, Mellgren SI, Mygland Å, Tallaksen C, Andersen H, Terkelsen AJ, Fontain F, Hietaharju A. Samuelsson K, et al. Among authors: mellgren si. Muscle Nerve. 2019 Mar;59(3):354-357. doi: 10.1002/mus.26348. Epub 2018 Dec 4. Muscle Nerve. 2019. PMID: 30246259
Two novel SCN9A mutations causing insensitivity to pain.
Nilsen KB, Nicholas AK, Woods CG, Mellgren SI, Nebuchennykh M, Aasly J. Nilsen KB, et al. Among authors: mellgren si. Pain. 2009 May;143(1-2):155-8. doi: 10.1016/j.pain.2009.02.016. Epub 2009 Mar 21. Pain. 2009. PMID: 19304393
160 results