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Hereditary systemic amyloidosis due to Asp76Asn variant β2-microglobulin.
Valleix S, Gillmore JD, Bridoux F, Mangione PP, Dogan A, Nedelec B, Boimard M, Touchard G, Goujon JM, Lacombe C, Lozeron P, Adams D, Lacroix C, Maisonobe T, Planté-Bordeneuve V, Vrana JA, Theis JD, Giorgetti S, Porcari R, Ricagno S, Bolognesi M, Stoppini M, Delpech M, Pepys MB, Hawkins PN, Bellotti V. Valleix S, et al. Among authors: adams d. N Engl J Med. 2012 Jun 14;366(24):2276-83. doi: 10.1056/NEJMoa1201356. N Engl J Med. 2012. PMID: 22693999 Free article.
Monoclonal gammopathy and neuropathy.
Lozeron P, Adams D. Lozeron P, et al. Among authors: adams d. Curr Opin Neurol. 2007 Oct;20(5):536-41. doi: 10.1097/WCO.0b013e3282ef79e3. Curr Opin Neurol. 2007. PMID: 17885441 Review.
[Metabolic neuropathies].
Lozeron P, Adams D. Lozeron P, et al. Among authors: adams d. Rev Prat. 2008 Nov 15;58(17):1903-9. Rev Prat. 2008. PMID: 19157206 French.
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. 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. Curr Opin Neurol. 2012 Oct;25(5):564-72. doi: 10.1097/WCO.0b013e328357bdf6. Curr Opin Neurol. 2012. PMID: 22941262 Review.
[Autonomic peripheral neuropathy].
Adams D, Cauquil C, Lozeron P. Adams D, et al. Presse Med. 2012 Nov;41(11):1128-36. doi: 10.1016/j.lpm.2012.05.030. Epub 2012 Sep 27. Presse Med. 2012. PMID: 23021660 Review. French.
5,689 results