Ausgewählte Publikationen 2010
Morice-Picard F, Léauté-Labrèze C, Décor A, Boralevi F, Lacombe D, Taieb A, Fischer J. A novel mutation in the fatty acid transport protein 4 gene in a patient initially described as affected by self-healing congenital verruciform hyperkeratosis. Am J Med Genet A. 2010, 152A:2664-2665.
Oji V, Tadini G, Akiyama M, Blanchet Bardon C, Bodemer C, Bourrat E, Coudiere P, DiGiovanna JJ, Elias P, Fischer J, Fleckman P, Gina M, Harper J, Hashimoto T, Hausser I, Hennies H-C, Hohl D, Hovnanian A, Ishida-Yamamoto A, Jacyk WJ Leachman S, Leigh I, Mazereeuw-Hautier J, Milstone L, Morice-Picard F, Paller A, Richard G, Matthias Schmuth M, Shimizu H, Sprecher E, Van Steensel M, Taïeb A, Toro J, Vabres P, Vahlquist A, Williams M, Traupe H. Revised nomenclature and classification of inherited ichthyoses: Results of the First Ichthyosis Consensus Conference in Sorèze 2009, Journal of the Amercican Academy of Dermatology JAAD 2010 63:607-641.
Vahlquist A, Bygum A, Gånemo A, Virtanen M, Hellström-Pigg M, Strauss G, Brandrup F, and Fischer J. Genotypic and clinical spectrum of self-improving collodion ichthyosis: ALOX12B, ALOXE3 and TGM1 mutations in Scandinavian patients. J Invest Dermatol. 2010, 130:438-43