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487 results

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Page 1
[Isolated neonatal dysfunction of brainstem].
Abadie V, Chéron G, Lyonnet S, Hubert P, Morisseau-Durand MP, Jan D, Manac'h Y, Couly G. Abadie V, et al. Among authors: lyonnet s. Arch Pediatr. 1996 Feb;3(2):130-6. doi: 10.1016/0929-693x(96)85063-9. Arch Pediatr. 1996. PMID: 8785532 French.
[Dysfunction of the brain stem and congenital heart defects].
Abadie V, Bonnet D, Lyonnet S, Couly G. Abadie V, et al. Among authors: lyonnet s. Arch Pediatr. 2000 May;7 Suppl 2:145s-149s. doi: 10.1016/s0929-693x(00)80016-0. Arch Pediatr. 2000. PMID: 10904689 French. No abstract available.
[Pregnancy and the child of a mother with phenylketonuria].
Abadie V, Depondt E, Farriaux JP, Lepercq J, Lyonnet S, Maurin N, Ogier de Baulny H, Vidailhet M. Abadie V, et al. Among authors: lyonnet s. Arch Pediatr. 1996 May;3(5):489-6. doi: 10.1016/0929-693x(96)86411-6. Arch Pediatr. 1996. PMID: 8763723 Review. French.
CHARGE syndrome: report of 47 cases and review.
Tellier AL, Cormier-Daire V, Abadie V, Amiel J, Sigaudy S, Bonnet D, de Lonlay-Debeney P, Morrisseau-Durand MP, Hubert P, Michel JL, Jan D, Dollfus H, Baumann C, Labrune P, Lacombe D, Philip N, LeMerrer M, Briard ML, Munnich A, Lyonnet S. Tellier AL, et al. Among authors: lyonnet s. Am J Med Genet. 1998 Apr 13;76(5):402-9. doi: 10.1002/(sici)1096-8628(19980413)76:5<402::aid-ajmg7>3.0.co;2-o. Am J Med Genet. 1998. PMID: 9556299 Review.
Pierre Robin sequence: a series of 117 consecutive cases.
Holder-Espinasse M, Abadie V, Cormier-Daire V, Beyler C, Manach Y, Munnich A, Lyonnet S, Couly G, Amiel J. Holder-Espinasse M, et al. Among authors: lyonnet s. J Pediatr. 2001 Oct;139(4):588-90. doi: 10.1067/mpd.2001.117784. J Pediatr. 2001. PMID: 11598609
Early prognostic factors for intellectual outcome in CHARGE syndrome.
Raqbi F, Le Bihan C, Morisseau-Durand MP, Dureau P, Lyonnet S, Abadie V. Raqbi F, et al. Among authors: lyonnet s. Dev Med Child Neurol. 2003 Jul;45(7):483-8. doi: 10.1017/s0012162203000896. Dev Med Child Neurol. 2003. PMID: 12828403 Free article.
Temporal bone anomaly proposed as a major criteria for diagnosis of CHARGE syndrome.
Amiel J, Attieé-Bitach T, Marianowski R, Cormier-Daire V, Abadie V, Bonnet D, Gonzales M, Chemouny S, Brunelle F, Munnich A, Manach Y, Lyonnet S. Amiel J, et al. Among authors: lyonnet s. Am J Med Genet. 2001 Mar 1;99(2):124-7. doi: 10.1002/1096-8628(20010301)99:2<124::aid-ajmg1114>3.0.co;2-9. Am J Med Genet. 2001. PMID: 11241470
Features of DiGeorge syndrome and CHARGE association in five patients.
de Lonlay-Debeney P, Cormier-Daire V, Amiel J, Abadie V, Odent S, Paupe A, Couderc S, Tellier AL, Bonnet D, Prieur M, Vekemans M, Munnich A, Lyonnet S. de Lonlay-Debeney P, et al. Among authors: lyonnet s. J Med Genet. 1997 Dec;34(12):986-9. doi: 10.1136/jmg.34.12.986. J Med Genet. 1997. PMID: 9429139 Free PMC article.
487 results