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Page 1
[Diagnosis of mucoviscidosis].
Storni V, Claustres M, Chinet T, Ravilly S. Storni V, et al. Arch Pediatr. 2001 Dec;8 Suppl 5:818s-832s. doi: 10.1016/s0929-693x(01)80003-8. Arch Pediatr. 2001. PMID: 11811051 French. No abstract available.
[Joubert's syndrome].
Buissonnière RF, Storni V, Robain O, Ponsot G. Buissonnière RF, et al. Among authors: storni v. Ann Pediatr (Paris). 1990 Mar;37(3):151-6. Ann Pediatr (Paris). 1990. PMID: 2190521 Review. French.
Association of 1078 del T cystic fibrosis mutation with severe disease.
Moullier P, Jéhanne M, Audrézet MP, Mercier B, Verlingue C, Quéré I, Guillermit H, Raguénès O, Storni V, Rault G, et al. Moullier P, et al. Among authors: storni v. J Med Genet. 1994 Feb;31(2):159-61. doi: 10.1136/jmg.31.2.159. J Med Genet. 1994. PMID: 7514227 Free PMC article.
Comparing the clinical evolution of cystic fibrosis screened neonatally to that of cystic fibrosis diagnosed from clinical symptoms: a 10-year retrospective study in a French region (Brittany).
Siret D, Bretaudeau G, Branger B, Dabadie A, Dagorne M, David V, de Braekeleer M, Moisan-Petit V, Picherot G, Rault G, Storni V, Roussey M. Siret D, et al. Among authors: storni v. Pediatr Pulmonol. 2003 May;35(5):342-9. doi: 10.1002/ppul.10259. Pediatr Pulmonol. 2003. PMID: 12687590