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Genotype-phenotype correlation and course of transthyretin familial amyloid polyneuropathies in France.
Mariani LL, Lozeron P, Théaudin M, Mincheva Z, Signate A, Ducot B, Algalarrondo V, Denier C, Adam C, Nicolas G, Samuel D, Slama MS, Lacroix C, Misrahi M, Adams D; French Familial Amyloid Polyneuropathies Network (CORNAMYL) Study Group. Mariani LL, et al. Among authors: lacroix c. Ann Neurol. 2015 Dec;78(6):901-16. doi: 10.1002/ana.24519. Epub 2015 Oct 7. Ann Neurol. 2015. PMID: 26369527 Free PMC article.
Regional difference and similarity of familial amyloidosis with polyneuropathy in France.
Adams D, Lozeron P, Theaudin M, Mincheva Z, Cauquil C, Adam C, Signate A, Vial C, Maisonobe T, Delmont E, Franques J, Vallat JM, Sole G, Pereon Y, Lacour A, Echaniz-Laguna A, Misrahi M, Lacroix C; French Network for FAP. Adams D, et al. Among authors: lacroix c. Amyloid. 2012 Jun;19 Suppl 1:61-4. doi: 10.3109/13506129.2012.685665. Amyloid. 2012. PMID: 22620968
Amyloid neuropathies.
Adams D, Lozeron P, Lacroix C. Adams D, et al. Among authors: lacroix c. Curr Opin Neurol. 2012 Oct;25(5):564-72. doi: 10.1097/WCO.0b013e328357bdf6. Curr Opin Neurol. 2012. PMID: 22941262 Review.
Upper limb onset of hereditary transthyretin amyloidosis is common in non-endemic areas.
Théaudin M, Lozeron P, Algalarrondo V, Lacroix C, Cauquil C, Labeyrie C, Slama MS, Adam C, Guiochon-Mantel A, Adams D; French FAP Network (CORNAMYL) Study Group. Théaudin M, et al. Among authors: lacroix c. Eur J Neurol. 2019 Mar;26(3):497-e36. doi: 10.1111/ene.13845. Epub 2018 Dec 11. Eur J Neurol. 2019. PMID: 30350904
753 results