Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Catherine Eschard"'
Autor:
Annabel Maruani, Marine Durieux-Verde, Juliette Mazereeuw-Hautier, Olivia Boccara, Ludovic Martin, Christine Chiaverini, Catherine Eschard, Nathalie Bénéton, Pierre Vabres, Xavier Balguerie, Patrice Plantin, Didier Bessis, Sébastien Barbarot, Ali Dadban, Catherine Droitcourt, Aline Berthelot, Gérard Lorette, Sophie Leducq, Mahtab Samimi, Christian Andres, Agnès Caille, Patrick Vourc'h, Groupe de Recherche de la Société Française de Dermatologie
Publikováno v:
Acta Dermato-Venereologica, Vol 98, Iss 2, Pp 251-255 (2017)
Patients with an inherited autosomal-dominant disorder, capillary malformation–arteriovenous malformation (CM-AVM), frequently have mutations in Ras P21 protein activator 1 (RASA1). The aims of this study were to determine the prevalence of germlin
Externí odkaz:
https://doaj.org/article/14c6109276f84b4bace541a7171240e8
Autor:
Charlée Nardin, Olivia Boccara, Catherine Eschard, Michael Bayaram, Thibaud Dabudyk, François Aubin, Eve Puzenat
Publikováno v:
Acta Dermato-Venereologica, Vol 97, Iss 7, Pp 851-852 (2017)
Externí odkaz:
https://doaj.org/article/03f52123086d4d0bbed8d09beaa277ca
Autor:
Bernard Kalis, Catherine Eschard, Anne-Marie Prieur, Philippe Bernard M.D., Christophe Leys, Jacques Motte
Publikováno v:
Pediatric Dermatology. 22:222-226
We report an 11-month-old boy of French origin who had chronic, infantile, neurological, cutaneous, and articular syndrome with a particularly severe joint involvement with early onset. The diagnosis was based on the association of neurologic, cutane
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7da37abbd21cb0fc6fd125f11d73d1d
https://doi.org/10.1111/j.1525-1470.2005.22316.x
https://doi.org/10.1111/j.1525-1470.2005.22316.x
Autor:
Christine Léauté-Labrèze, Khaled Ezzedine, Alain Taieb, Sébastien Barbarot, Juliette Mazereeuw-Hautier, Catherine Eschard, Franck Boralevi, Sorilla Prey
Publikováno v:
Pediatric dermatology. 30(4)
Idiopathic facial aseptic granuloma (IFAG) is a disorder that usually occurs during early childhood. Its pathogenesis remains poorly understood. The objective of this study was to investigate possible relationships between IFAG and childhood rosacea.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38e6edf3e011eaa3ed1c79fdbdaed828
https://pubmed.ncbi.nlm.nih.gov/23560522
https://pubmed.ncbi.nlm.nih.gov/23560522