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Page 1
Incidence of cardiovascular events and risk markers in a prospective study of children diagnosed with Marfan syndrome.
Hascoet S, Edouard T, Plaisancie J, Arnoult F, Milleron O, Stheneur C, Chevallier B, Zordan C, Odent S, Bal L, Faivre L, Leheup B, Dupuis-Girod S, Ruidavets JB, Acar P, Ferrieres J, Jondeau G, Dulac Y. Hascoet S, et al. Among authors: stheneur c. Arch Cardiovasc Dis. 2020 Jan;113(1):40-49. doi: 10.1016/j.acvd.2019.09.010. Epub 2019 Nov 14. Arch Cardiovasc Dis. 2020. PMID: 31735609 Free article.
Comparison of clinical presentations and outcomes between patients with TGFBR2 and FBN1 mutations in Marfan syndrome and related disorders.
Attias D, Stheneur C, Roy C, Collod-Béroud G, Detaint D, Faivre L, Delrue MA, Cohen L, Francannet C, Béroud C, Claustres M, Iserin F, Khau Van Kien P, Lacombe D, Le Merrer M, Lyonnet S, Odent S, Plauchu H, Rio M, Rossi A, Sidi D, Steg PG, Ravaud P, Boileau C, Jondeau G. Attias D, et al. Among authors: stheneur c. Circulation. 2009 Dec 22;120(25):2541-9. doi: 10.1161/CIRCULATIONAHA.109.887042. Epub 2009 Dec 7. Circulation. 2009. PMID: 19996017 Free article.
Spinal imaging contributes to the diagnosis of Marfan syndrome.
Sznajder M, Krug P, Taylor M, Moura B, Leparc JM, Boileau C, Jondeau G, Chevallier B, Pelage JP, Stheneur C. Sznajder M, et al. Among authors: stheneur c. Joint Bone Spine. 2010 Oct;77(5):445-50. doi: 10.1016/j.jbspin.2010.02.031. Epub 2010 May 8. Joint Bone Spine. 2010. PMID: 20452804
Prognosis factors in probands with an FBN1 mutation diagnosed before the age of 1 year.
Stheneur C, Faivre L, Collod-Béroud G, Gautier E, Binquet C, Bonithon-Kopp C, Claustres M, Child AH, Arbustini E, Adès LC, Francke U, Mayer K, Arslan-Kirchner M, De Paepe A, Chevallier B, Bonnet D, Jondeau G, Boileau C. Stheneur C, et al. Pediatr Res. 2011 Mar;69(3):265-70. doi: 10.1203/PDR.0b013e3182097219. Pediatr Res. 2011. PMID: 21135753 Free article.
[Recent progress in Marfan syndrome].
Stheneur C, Laffond C, Rioux S, Benoist G, Chevallier B, Jondeau G. Stheneur C, et al. Arch Pediatr. 2012 May;19(5):551-5. doi: 10.1016/j.arcped.2012.02.004. Epub 2012 Mar 21. Arch Pediatr. 2012. PMID: 22440060 French.
[Multidisciplinary management and paediatric Marfan syndrome].
Chevallier B, Oberkampf B, Stheneur C. Chevallier B, et al. Among authors: stheneur c. Arch Pediatr. 2008 Jun;15(5):582-3. doi: 10.1016/S0929-693X(08)71840-2. Arch Pediatr. 2008. PMID: 18582679 French. No abstract available.
Identification of 23 TGFBR2 and 6 TGFBR1 gene mutations and genotype-phenotype investigations in 457 patients with Marfan syndrome type I and II, Loeys-Dietz syndrome and related disorders.
Stheneur C, Collod-Béroud G, Faivre L, Gouya L, Sultan G, Le Parc JM, Moura B, Attias D, Muti C, Sznajder M, Claustres M, Junien C, Baumann C, Cormier-Daire V, Rio M, Lyonnet S, Plauchu H, Lacombe D, Chevallier B, Jondeau G, Boileau C. Stheneur C, et al. Hum Mutat. 2008 Nov;29(11):E284-95. doi: 10.1002/humu.20871. Hum Mutat. 2008. PMID: 18781618 Free article.
75 results