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Page 1
Proceedings of the annual meeting of the European Consortium of Lipodystrophies (ECLip), Pisa, Italy, 28-29 September 2023.
Ceccarini G, Akinci B, Araujo-Vilar D, Beghini M, Brown RJ, Carrion Tudela J, Corradin V, Donadille B, Jerez Ruiz J, Jeru I, Lattanzi G, Maffei M, McIlroy GD, Nobécourt E, Perez de Tudela N, Rochford JJ, Sanders R, von Schnurbein J, Tews D, Vantyghem MC, Vatier C, Vigouroux C, Santini F. Ceccarini G, et al. Among authors: donadille b. Ann Endocrinol (Paris). 2024 Mar 5:S0003-4266(24)00036-2. doi: 10.1016/j.ando.2024.03.002. Online ahead of print. Ann Endocrinol (Paris). 2024. PMID: 38452868
New metabolic phenotypes in laminopathies: LMNA mutations in patients with severe metabolic syndrome.
Decaudain A, Vantyghem MC, Guerci B, Hécart AC, Auclair M, Reznik Y, Narbonne H, Ducluzeau PH, Donadille B, Lebbé C, Béréziat V, Capeau J, Lascols O, Vigouroux C. Decaudain A, et al. Among authors: donadille b. J Clin Endocrinol Metab. 2007 Dec;92(12):4835-44. doi: 10.1210/jc.2007-0654. Epub 2007 Aug 21. J Clin Endocrinol Metab. 2007. PMID: 17711925
Partial lipodystrophy with severe insulin resistance and adult progeria Werner syndrome.
Donadille B, D'Anella P, Auclair M, Uhrhammer N, Sorel M, Grigorescu R, Ouzounian S, Cambonie G, Boulot P, Laforêt P, Carbonne B, Christin-Maitre S, Bignon YJ, Vigouroux C. Donadille B, et al. Orphanet J Rare Dis. 2013 Jul 12;8:106. doi: 10.1186/1750-1172-8-106. Orphanet J Rare Dis. 2013. PMID: 23849162 Free PMC article.
Cardiovascular complications of lipodystrophic syndromes - focus on laminopathies.
Mosbah H, Vatier C, Boccara F, Jéru I, Vantyghem MC, Donadille B, Wahbi K, Vigouroux C. Mosbah H, et al. Among authors: donadille b. Ann Endocrinol (Paris). 2021 Jun;82(3-4):146-148. doi: 10.1016/j.ando.2020.03.002. Epub 2020 Mar 4. Ann Endocrinol (Paris). 2021. PMID: 32201029 No abstract available.
Looking at New Unexpected Disease Targets in LMNA-Linked Lipodystrophies in the Light of Complex Cardiovascular Phenotypes: Implications for Clinical Practice.
Mosbah H, Vatier C, Boccara F, Jéru I, Lascols O, Vantyghem MC, Fève B, Donadille B, Sarrazin E, Benabbou S, Inamo J, Ederhy S, Cohen A, Neraud B, Richard P, Picard F, Christin-Maitre S, Redheuil A, Wahbi K, Vigouroux C. Mosbah H, et al. Among authors: donadille b. Cells. 2020 Mar 20;9(3):765. doi: 10.3390/cells9030765. Cells. 2020. PMID: 32245113 Free PMC article.
Molecular and Cellular Bases of Lipodystrophy Syndromes.
Zammouri J, Vatier C, Capel E, Auclair M, Storey-London C, Bismuth E, Mosbah H, Donadille B, Janmaat S, Fève B, Jéru I, Vigouroux C. Zammouri J, et al. Among authors: donadille b. Front Endocrinol (Lausanne). 2022 Jan 3;12:803189. doi: 10.3389/fendo.2021.803189. eCollection 2021. Front Endocrinol (Lausanne). 2022. PMID: 35046902 Free PMC article. Review.
Dunnigan lipodystrophy syndrome: French National Diagnosis and Care Protocol (PNDS; Protocole National de Diagnostic et de Soins).
Mosbah H, Donadille B, Vatier C, Janmaat S, Atlan M, Badens C, Barat P, Béliard S, Beltrand J, Ben Yaou R, Bismuth E, Boccara F, Cariou B, Chaouat M, Charriot G, Christin-Maitre S, De Kerdanet M, Delemer B, Disse E, Dubois N, Eymard B, Fève B, Lascols O, Mathurin P, Nobécourt E, Poujol-Robert A, Prevost G, Richard P, Sellam J, Tauveron I, Treboz D, Vergès B, Vermot-Desroches V, Wahbi K, Jéru I, Vantyghem MC, Vigouroux C. Mosbah H, et al. Among authors: donadille b. Orphanet J Rare Dis. 2022 Apr 19;17(Suppl 1):170. doi: 10.1186/s13023-022-02308-7. Orphanet J Rare Dis. 2022. PMID: 35440056 Free PMC article.
Therapeutic indications and metabolic effects of metreleptin in patients with lipodystrophy syndromes: Real-life experience from a national reference network.
Mosbah H, Vantyghem MC, Nobécourt E, Andreelli F, Archambeaud F, Bismuth E, Briet C, Cartigny M, Chevalier B, Donadille B, Daguenel A, Fichet M, Gautier JF, Janmaat S, Jéru I, Legagneur C, Leguier L, Maitre J, Mongeois E, Poitou C, Renard E, Reznik Y, Spiteri A, Travert F, Vergès B, Zammouri J, Vigouroux C, Vatier C. Mosbah H, et al. Among authors: donadille b. Diabetes Obes Metab. 2022 Aug;24(8):1565-1577. doi: 10.1111/dom.14726. Epub 2022 May 12. Diabetes Obes Metab. 2022. PMID: 35445532 Free PMC article.
Patients' perspective on the medical pathway from first symptoms to diagnosis in genetic lipodystrophy.
Mosbah H, Vatier C, Andriss B, Belalem I, Delemer B, Janmaat S, Jéru I, Le Collen L, Maiter D, Nobécourt E, Vantyghem MC; Network « Pathologies Rares de l’Insulino-Sécrétion et de l’Insulino-Sensibilité » (PRISIS); Vigouroux C, Dumas A. Mosbah H, et al. Eur J Endocrinol. 2024 Jan 3;190(1):23-33. doi: 10.1093/ejendo/lvad169. Eur J Endocrinol. 2024. PMID: 38128113
53 results