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Hepatocyte growth factor measurement in AL amyloidosis.
Abraham J, Desport E, Rigaud C, Marin B, Bender S, Lacombe C, Moreau S, Yagoubi F, Bordessoule D, Lavergne D, Bridoux F, Jaccard A. Abraham J, et al. Among authors: lacombe c. Amyloid. 2015;22(2):112-6. doi: 10.3109/13506129.2015.1014548. Epub 2015 Jun 8. Amyloid. 2015. PMID: 26053104
Strategies to model AL amyloidosis in mice.
Sirac C, Bender S, Jaccard A, Bridoux F, Lacombe C, Touchard G, Cogné M. Sirac C, et al. Among authors: lacombe c. Amyloid. 2011 Jun;18 Suppl 1:45-7. doi: 10.3109/13506129.2011.574354016. Amyloid. 2011. PMID: 21838428 No abstract available.
Al amyloidosis.
Desport E, Bridoux F, Sirac C, Delbes S, Bender S, Fernandez B, Quellard N, Lacombe C, Goujon JM, Lavergne D, Abraham J, Touchard G, Fermand JP, Jaccard A; Centre national de référence pour l’amylose AL et les autres maladies par dépôts d’immunoglobulines monoclonales. Desport E, et al. Among authors: lacombe c. Orphanet J Rare Dis. 2012 Aug 21;7:54. doi: 10.1186/1750-1172-7-54. Orphanet J Rare Dis. 2012. PMID: 22909024 Free PMC article. Review.
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: lacombe c. N Engl J Med. 2012 Jun 14;366(24):2276-83. doi: 10.1056/NEJMoa1201356. N Engl J Med. 2012. PMID: 22693999 Free article.
Priapism revealing ARG 506 to GLN factor V mutation.
de Prost D, Delmas V, Lefebvre M, Lacombe C, Bridey F. de Prost D, et al. Among authors: lacombe c. J Urol. 1996 Apr;155(4):1392. doi: 10.1097/00005392-199604000-00078. J Urol. 1996. PMID: 8632589 No abstract available.
331 results