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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1972 1
1979 1
1981 1
1984 1
1985 1
1986 1
1987 1
1989 1
1990 1
1992 1
1993 2
1994 1
1995 3
1996 3
1997 1
1998 6
1999 4
2000 2
2001 1
2002 3
2003 2
2004 3
2005 7
2006 7
2007 6
2008 3
2009 5
2010 5
2011 4
2012 4
2013 1
2014 2
2015 3
2024 0

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81 results

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Page 1
[Turner syndrome].
Cabrol S. Cabrol S. Ann Endocrinol (Paris). 2007 Feb;68(1):2-9. doi: 10.1016/j.ando.2006.12.002. Epub 2007 Feb 22. Ann Endocrinol (Paris). 2007. PMID: 17320033 Review. French.
[Postembolic pulmonary hypertension].
Jais X, Dartevelle P, Parent F, Sitbon O, Humbert M, Fadel E, Mussot S, Cabrol S, Le Pavec J, Sztrymf B, Tcherakian C, Musset D, Maitre S, Simonneau G. Jais X, et al. Among authors: cabrol s. Rev Mal Respir. 2007 Apr;24(4 Pt 1):497-508. doi: 10.1016/s0761-8425(07)91572-7. Rev Mal Respir. 2007. PMID: 17468706 Review. French.
[Treatment of pulmonary arterial hypertension].
Montani D, Sitbon O, Jaïs X, Cabrol S, Simonneau G, Humbert M. Montani D, et al. Among authors: cabrol s. Presse Med. 2005 Nov 5;34(19 Pt 2):1445-55. doi: 10.1016/s0755-4982(05)84206-x. Presse Med. 2005. PMID: 16301976 Review. French.
Molecular diagnosis of Turner's syndrome.
Gicquel C, Cabrol S, Schneid H, Girard F, Le Bouc Y. Gicquel C, et al. Among authors: cabrol s. J Med Genet. 1992 Aug;29(8):547-51. doi: 10.1136/jmg.29.8.547. J Med Genet. 1992. PMID: 1355559 Free PMC article.
[BCG osteitis].
Berger JP, Chambenoit J, Cabrol S, Lasfargues G, Carlioz H. Berger JP, et al. Among authors: cabrol s. Arch Fr Pediatr. 1979 May;36(5):493-7. Arch Fr Pediatr. 1979. PMID: 496543 French. No abstract available.
[Massive hemoptysis during sarcoidosis].
Cabrol S, Morel H, Qanadli S, Delaisement-Pol C, Labrune S, Bisson A, Huchon G, Chinet T. Cabrol S, et al. Rev Mal Respir. 2000 Dec;17(6):1111-3. Rev Mal Respir. 2000. PMID: 11217510 French.
Natural history and management of congenital hypothyroidism with in situ thyroid gland.
Castanet M, Goischke A, Léger J, Thalassinos C, Rodrigue D, Cabrol S, Zenaty D, al-Harbi M, Polak M, Czernichow P; Fédération Parisienne pour le Dépistage et la Prévention des Handicaps de l''Enfant (FDPHE). Castanet M, et al. Among authors: cabrol s. Horm Res Paediatr. 2015;83(2):102-10. doi: 10.1159/000362234. Epub 2015 Jan 28. Horm Res Paediatr. 2015. PMID: 25634148
Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome.
Dodé C, Levilliers J, Dupont JM, De Paepe A, Le Dû N, Soussi-Yanicostas N, Coimbra RS, Delmaghani S, Compain-Nouaille S, Baverel F, Pêcheux C, Le Tessier D, Cruaud C, Delpech M, Speleman F, Vermeulen S, Amalfitano A, Bachelot Y, Bouchard P, Cabrol S, Carel JC, Delemarre-van de Waal H, Goulet-Salmon B, Kottler ML, Richard O, Sanchez-Franco F, Saura R, Young J, Petit C, Hardelin JP. Dodé C, et al. Among authors: cabrol s. Nat Genet. 2003 Apr;33(4):463-5. doi: 10.1038/ng1122. Epub 2003 Mar 10. Nat Genet. 2003. PMID: 12627230
81 results