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Page 1
AA amyloidosis complicating monoclonal gammopathies, an unusual feature validating the concept of "monoclonal gammopathy of inflammatory significance"?
Terré A, Colombat M, Cez A, Martin C, Diet C, Brechignac S, Oghina S, Bodez D, Faguer S, Savey L, Galland J, Boffa JJ, Grateau G, Jaccard A, Buob D, Georgin-Lavialle S. Terré A, et al. Among authors: colombat m. Int J Clin Pract. 2021 Nov;75(11):e14817. doi: 10.1111/ijcp.14817. Epub 2021 Sep 21. Int J Clin Pract. 2021. PMID: 34490695 Review.
Mass spectrometry-based proteomics in clinical practice amyloid typing: state-of-the-art from a French nationwide cohort.
Colombat M, Gaspard M, Camus M, Dalloux-Chioccioli J, Delas A, Poullot E, Moktefi A, François A, Moreau A, Gibier JB, Raynaud P, Huart A, Piedrafita A, Gilhodes J, Lairez O, Grateau G, Georgin-Lavialle S, Maisonneuve H, Moreau P, Jaccard A, Bridoux F, Plante-Bordeneuve V, Damy T, Mal H, Brousset P, Valleix S, Burlet-Schiltz O. Colombat M, et al. Haematologica. 2022 Dec 1;107(12):2983-2987. doi: 10.3324/haematol.2022.281431. Haematologica. 2022. PMID: 35924579 Free PMC article. No abstract available.
New clinical forms of hereditary apoA-I amyloidosis entail both glomerular and retinal amyloidosis.
Colombat M, Aldigier JC, Rothschild PR, Javaugue V, Desport E, Frouget T, Goujon JM, Rioux-Leclercq N, Quellard N, Rerolle JP, Paraf F, Beugnet C, Tiple A, Durrbach A, Samuel D, Brézin A, Bridoux F, Valleix S. Colombat M, et al. Kidney Int. 2020 Jul;98(1):195-208. doi: 10.1016/j.kint.2020.03.033. Epub 2020 Apr 23. Kidney Int. 2020. PMID: 32571483 Free article.
Clinical and morphologic spectrum of renal involvement in patients with mixed cryoglobulinemia without evidence of hepatitis C virus infection.
Matignon M, Cacoub P, Colombat M, Saadoun D, Brocheriou I, Mougenot B, Roudot-Thoraval F, Vanhille P, Moranne O, Hachulla E, Hatron PY, Fermand JP, Fakhouri F, Ronco P, Plaisier E, Grimbert P. Matignon M, et al. Among authors: colombat m. Medicine (Baltimore). 2009 Nov;88(6):341-348. doi: 10.1097/MD.0b013e3181c1750f. Medicine (Baltimore). 2009. PMID: 19910748 Free article.
LC-MS/MS and immuno-electron subtyping combined with genetics show that OSMR mutations cause amyloid deposition of keratins 5/14 in familial primary localized cutaneous amyloidosis.
Bourguiba R, Bachmeyer C, Moguelet P, Kaaki S, Ory C, Touchard G, Cattan E, Georgin-Lavialle S, Colombat M, Valleix S. Bourguiba R, et al. Among authors: colombat m. J Eur Acad Dermatol Venereol. 2022 Jan;36(1):e66-e68. doi: 10.1111/jdv.17630. Epub 2021 Sep 17. J Eur Acad Dermatol Venereol. 2022. PMID: 34459039 No abstract available.
French brain tumor database: 5-year histological results on 25 756 cases.
Rigau V, Zouaoui S, Mathieu-Daudé H, Darlix A, Maran A, Trétarre B, Bessaoud F, Bauchet F, Attaoua R, Fabbro-Peray P, Fabbro M, Kerr C, Taillandier L, Duffau H, Figarella-Branger D, Costes V, Bauchet L; Société Française de Neuropathologie (SFNP), Société Française de Neurochirurgie (SFNC); Club de Neuro-Oncologie of the Société Française de Neurochirurgie (CNO-SFNC); Association des Neuro-Oncologues d’Expression Française (ANOCEF). Rigau V, et al. Brain Pathol. 2011 Nov;21(6):633-44. doi: 10.1111/j.1750-3639.2011.00491.x. Epub 2011 Jul 25. Brain Pathol. 2011. PMID: 21554472 Free PMC article.
127 results