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Page 1
A novel developmental and immunodeficiency syndrome associated with intrauterine growth retardation and a lack of natural killer cells.
Bernard F, Picard C, Cormier-Daire V, Eidenschenk C, Pinto G, Bustamante JC, Jouanguy E, Teillac-Hamel D, Colomb V, Funck-Brentano I, Pascal V, Vivier E, Fischer A, Le Deist F, Casanova JL. Bernard F, et al. Among authors: teillac hamel d. Pediatrics. 2004 Jan;113(1 Pt 1):136-41. doi: 10.1542/peds.113.1.136. Pediatrics. 2004. PMID: 14702466
Chronic infantile neurological cutaneous and articular syndrome is caused by mutations in CIAS1, a gene highly expressed in polymorphonuclear cells and chondrocytes.
Feldmann J, Prieur AM, Quartier P, Berquin P, Certain S, Cortis E, Teillac-Hamel D, Fischer A, de Saint Basile G. Feldmann J, et al. Among authors: teillac hamel d. Am J Hum Genet. 2002 Jul;71(1):198-203. doi: 10.1086/341357. Epub 2002 May 24. Am J Hum Genet. 2002. PMID: 12032915 Free PMC article.
[Nijmegen's syndrome].
Kunz B, Teillac Hamel D, Girier B, Stephan JL, De Prost Y. Kunz B, et al. Ann Dermatol Venereol. 1992;119(11):815-6. Ann Dermatol Venereol. 1992. PMID: 1301683 French. No abstract available.
[Rothmund-Thomson syndrome with reduced DNA repair capacity].
Prache-de-Carrère B, Teillac-Hamel D, Capesius C, Castelneau JP, Robert C, Fraitag S, de Prost Y. Prache-de-Carrère B, et al. Ann Dermatol Venereol. 1996;123(6-7):395-7. Ann Dermatol Venereol. 1996. PMID: 8959064 French.
[Kasabach-Merritt syndrome in children].
Teillac-Hamel D, Andry P, Bodemer C, Hubert P, Sebag G, Brunelle F, Nihoul-Fékété C, de Prost Y. Teillac-Hamel D, et al. Ann Pediatr (Paris). 1992 Sep;39(7):435-41. Ann Pediatr (Paris). 1992. PMID: 1416665 French.
28 results