C
Christine Labrèze
Researcher at Université catholique de Louvain
Publications - 6
Citations - 391
Christine Labrèze is an academic researcher from Université catholique de Louvain. The author has contributed to research in topics: Medicine & Patch test. The author has an hindex of 4, co-authored 6 publications receiving 348 citations.
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Journal ArticleDOI
Parkes Weber syndrome, vein of galen aneurysmal malformation, and other fast-flow vascular anomalies are caused by RASA1 mutations
Nicole Revencu,Laurence M. Boon,John B. Mulliken,Odile Enjolras,Maria R. Cordisco,Patricia E. Burrows,Philippe Clapuyt,Frank Hammer,Josée Dubois,Eulalia Baselga,Francesco Brancati,Robin Carder,José Miguel Ceballos Quintal,Bruno Dallapiccola,Gayle Fischer,Ilona J. Frieden,Maria C. Garzon,John Harper,Jennifer Johnson-Patel,Christine Labrèze,Loreto Martorell,Harriet J. Paltiel,Annette Pohl,Julie S. Prendiville,Isabelle Quéré,Dawn H. Siegel,Enza Maria Valente,Annet Van Hagen,Liselot Van Hest,Keith K. Vaux,Asunción Vicente,Lisa Weibel,David Chitayat,Miikka Vikkula +33 more
TL;DR: This first extensive study on the phenotypes associated with RASA1 mutations, and unravels their wide heterogeneity is reported, finding some CM‐AVM patients had neural tumors reminiscent of neurofibromatosis type 1 or 2.
Journal ArticleDOI
Aluminium sensitization in a French paediatric patch test population.
TL;DR: The objective of this study was to determine the prevalence of contact sensitization to aluminium in a paediatric population consulting for patch testing in a French paediatric dermatology department, and to study the association of the sensitization with persistent itching nodules.
Journal Article
SACRAL syndrome. Author's reply
Journal ArticleDOI
Management of Congenital Nevi at a Dermatologic Surgical Paediatric Outpatient Clinic: Consequences of an Audit Survey 1990–1997
Delphine Mérigou,Sorilla Prey,Pascal Niamba,Maya Loot,Sébastien Lepreux,Franck Boralevi,Christine Labrèze,P. Vergnes,Alain Taïeb +8 more
TL;DR: Nevus recurrence in cases operated early suggests a time-dependent phenomenon in nevogenesis, and early counselling is important as early surgery seems associated with a better scar quality.
Journal ArticleDOI
Keratitis-Ichthyosis-Deafness Syndrome: Early Death Caused by the GJB2 Mutation p.Gly12Arg.
Clothilde Godillot,M. Severino-Freire,Vincent Michaud,Franck Boralevi,Christine Labrèze,Vincent Guigonis,G. Onnis,Fanny Morice-Picard,Juliette Mazereeuw-Hautier +8 more
TL;DR: A new case of KID syndrome with early childhood death caused by the GJB2 mutation p.Gly12Arg is reported, which is an autosomal dominant condition with some familial cases, but the majority of cases are sporadic.