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Page 1
New mutations of CIAS1 that are responsible for Muckle-Wells syndrome and familial cold urticaria: a novel mutation underlies both syndromes.
Dodé C, Le Dû N, Cuisset L, Letourneur F, Berthelot JM, Vaudour G, Meyrier A, Watts RA, Scott DG, Nicholls A, Granel B, Frances C, Garcier F, Edery P, Boulinguez S, Domergues JP, Delpech M, Grateau G. Dodé C, et al. Among authors: vaudour g. Am J Hum Genet. 2002 Jun;70(6):1498-506. doi: 10.1086/340786. Epub 2002 Apr 25. Am J Hum Genet. 2002. PMID: 11992256 Free PMC article.
Genetic linkage of the Muckle-Wells syndrome to chromosome 1q44.
Cuisset L, Drenth JP, Berthelot JM, Meyrier A, Vaudour G, Watts RA, Scott DG, Nicholls A, Pavek S, Vasseur C, Beckmann JS, Delpech M, Grateau G. Cuisset L, et al. Among authors: vaudour g. Am J Hum Genet. 1999 Oct;65(4):1054-9. doi: 10.1086/302589. Am J Hum Genet. 1999. PMID: 10486324 Free PMC article.
Hypereosinophilia and Hypereosinophilic Syndromes: First Findings From a Nationwide Multicenter Cohort.
Lefèvre G, Bleuse S, Puyade M, Moulis G, Néel A, Abisror N, Baudet A, Bonnotte B, Dion J, Dossier A, Grall M, Lifermann F, Limal N, Lioger B, Machelart I, Mohr C, Outh R, Queyrel-Moranne V, Slama B, Tréfond L, Abou Chahla W, Ackerman F, Belfeki N, Berezne A, Blade JS, Bouderbala MA, Chebrek S, Cottin V, De Almeida S, De Masson A, Dezoteux F, Goulenok T, Jachiet V, Jouvray M, Latu I, Ledoult E, Leurs A, Lugosi M, Martin M, Melboucy-Belkhir S, Morati-Hafsaoui C, Quemeneur T, Rohmer J, Roy-Peaud F, Sanges S, Schleinitz N, Staumont-Salle D, Taillé C, Terriou L, Tieulie N, Koenga JDE, Schwarb L, Panel K, Kahn JE, Groh M; COHESion study group. Lefèvre G, et al. Allergy. 2025 Jan 5. doi: 10.1111/all.16463. Online ahead of print. Allergy. 2025. PMID: 39757773
[Children who swallow air].
Lecine T, Michaud L, Gottrand F, Launay V, Faure C, Bonnevalle M, Vaudour G, Turck D. Lecine T, et al. Among authors: vaudour g. Arch Pediatr. 1998 Nov;5(11):1224-8. doi: 10.1016/s0929-693x(98)81240-2. Arch Pediatr. 1998. PMID: 9853061 French.
[Creutzfeldt-Jakob disease in 4 children treated with growth hormone].
Billette de Villemeur T, Gourmelen M, Beauvais P, Rodriguez D, Vaudour G, Deslys JP, Dormont D, Richard P, Richardet JM. Billette de Villemeur T, et al. Among authors: vaudour g. Rev Neurol (Paris). 1992;148(5):328-34. Rev Neurol (Paris). 1992. PMID: 1448646 Review. French.
[Water deprivation. An uncommon form of child abuse].
Desprez P, Vaudour G, Burguin C, Fiette C, Bouabdallaoui R, Malou E, el Hanache A, Noirot P. Desprez P, et al. Among authors: vaudour g. Arch Fr Pediatr. 1990 Apr;47(4):287-9. Arch Fr Pediatr. 1990. PMID: 2363618 French.
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