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Page 1
Lipodystrophy as a Late Effect after Stem Cell Transplantation.
Tews D, Schulz A, Denzer C, von Schnurbein J, Ceccarini G, Debatin KM, Wabitsch M. Tews D, et al. Among authors: ceccarini g. J Clin Med. 2021 Apr 8;10(8):1559. doi: 10.3390/jcm10081559. J Clin Med. 2021. PMID: 33917653 Free PMC article. Review.
European lipodystrophy registry: background and structure.
von Schnurbein J, Adams C, Akinci B, Ceccarini G, D'Apice MR, Gambineri A, Hennekam RCM, Jeru I, Lattanzi G, Miehle K, Nagel G, Novelli G, Santini F, Santos Silva E, Savage DB, Sbraccia P, Schaaf J, Sorkina E, Tanteles G, Vantyghem MC, Vatier C, Vigouroux C, Vorona E, Araújo-Vilar D, Wabitsch M. von Schnurbein J, et al. Among authors: ceccarini g. Orphanet J Rare Dis. 2020 Jan 15;15(1):17. doi: 10.1186/s13023-020-1295-y. Orphanet J Rare Dis. 2020. PMID: 31941540 Free PMC article.
Partial Lipodystrophy and LMNA p.R545H Variant.
Magno S, Ceccarini G, Barison A, Fabiani I, Giacomina A, Gilio D, Pelosini C, Rubegni A, Emdin M, Gatti GL, Santorelli FM, Sessa MR, Santini F. Magno S, et al. Among authors: ceccarini g. J Clin Med. 2021 Mar 9;10(5):1142. doi: 10.3390/jcm10051142. J Clin Med. 2021. PMID: 33803191 Free PMC article.
Autoimmunity in lipodystrophy syndromes.
Ceccarini G, Magno S, Gilio D, Pelosini C, Santini F. Ceccarini G, et al. Presse Med. 2021 Nov;50(3):104073. doi: 10.1016/j.lpm.2021.104073. Epub 2021 Sep 20. Presse Med. 2021. PMID: 34547374 Free article. Review.
Proceedings of the annual meeting of the European Consortium of Lipodystrophies (ECLip) Cambridge, UK, 7-8 April 2022.
Mosbah H, Akinci B, Araújo-Vilar D, Carrion Tudela J, Ceccarini G, Collas P, Farooqi IS, Fernández-Pombo A, Jéru I, Karpe F, Krause K, Maffei M, Miehle K, Oral E, Perez de Tudela N, Prieur X, Rochford J, Sanders R, Santini F, Savage DB, von Schnurbein J, Semple R, Stears A, Sorkina E, Vantyghem MC, Vatier C, Vidal-Puig A, Vigouroux C, Wabitsch M. Mosbah H, et al. Among authors: ceccarini g. Ann Endocrinol (Paris). 2022 Dec;83(6):461-468. doi: 10.1016/j.ando.2022.07.674. Epub 2022 Oct 4. Ann Endocrinol (Paris). 2022. PMID: 36206842
Clinical Characteristics of Patients With Acquired Partial Lipodystrophy: A Multicenter Retrospective Study.
Magno S, Ceccarini G, Corvillo F, Pelosini C, Gilio D, Paoli M, Fornaciari S, Pandolfo G, Sanchez-Iglesias S, Nozal P, Curcio M, Sessa MR, López-Trascasa M, Araújo-Vilar D, Santini F. Magno S, et al. Among authors: ceccarini g. J Clin Endocrinol Metab. 2024 Feb 20;109(3):e932-e944. doi: 10.1210/clinem/dgad700. J Clin Endocrinol Metab. 2024. PMID: 38061004
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. 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
Identification of a novel mutation in the polymerase delta 1 (POLD1) gene in a lipodystrophic patient affected by mandibular hypoplasia, deafness, progeroid features (MDPL) syndrome.
Pelosini C, Martinelli S, Ceccarini G, Magno S, Barone I, Basolo A, Fierabracci P, Vitti P, Maffei M, Santini F. Pelosini C, et al. Among authors: ceccarini g. Metabolism. 2014 Nov;63(11):1385-9. doi: 10.1016/j.metabol.2014.07.010. Epub 2014 Jul 25. Metabolism. 2014. PMID: 25131834
Atypical Progeroid Syndrome and Partial Lipodystrophy Due to LMNA Gene p.R349W Mutation.
Magno S, Ceccarini G, Pelosini C, Ferrari F, Prodam F, Gilio D, Maffei M, Sessa MR, Barison A, Ciccarone A, Emdin M, Aimaretti G, Santini F. Magno S, et al. Among authors: ceccarini g. J Endocr Soc. 2020 Aug 1;4(10):bvaa108. doi: 10.1210/jendso/bvaa108. eCollection 2020 Oct 1. J Endocr Soc. 2020. PMID: 32913962 Free PMC article.
85 results