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Items where Author is "Bruckner-Tuderman, Leena"

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Jump to: 2019 | 2014 | 2012 | 2010
Number of items: 4.

2019

Higgins, Rebecca and Jensen, Annika N. and Wachstein, Julian and Bruckner-Tuderman, Leena and Spiegel, Roland and Traber, Hubert and Achermann, Josef and Schaller, Martin and Fehrenbacher, Birgit and Röcken, Martin and Ignatova, Desislava and Chang, Yun-Tsan and Fischer, Tina and Schwieger-Briel, Agnes E. and French, Lars E. and Hoetzenecker, Wolfram and Hornung, René and Malzacher, Andreas and Cozzio, Antonio and Navarini, Alexander and Has, Cristina and Guenova, Emmanuella. (2019) Uniparental Disomy of Chromosome 2 Unmasks New ITGA6 Recessive Mutation and Results in a Lethal Junctional Epidermolysis Bullosa in a Newborn. Acta Dermato-Venereologica, 100 (1). pp. 1-3.

2014

Has, Cristina and Kiritsi, Dimitra and Mellerio, Jemima E. and Franzke, Claus-Werner and Wedgeworth, Emma and Tantcheva-Poor, Iliana and Kernland-Lang, Kristin and Itin, Peter and Simpson, Michael A. and Dopping-Hepenstal, Patricia J. and Fujimoto, Wataru and McGrath, John A. and Bruckner-Tuderman, Leena. (2014) The Missense Mutation p.R1303Q in Type XVII Collagen Underlies Junctional Epidermolysis Bullosa Resembling Kindler Syndrome. Journal of investigative dermatology, Vol. 134, H. 3. pp. 845-849.

2012

Arnold, Andreas W. and Kiritsi, Dimitra and Happle, Rudolf and Kohlhase, Jürgen and Hausser, Ingrid and Bruckner-Tuderman, Leena and Has, Cristina and Itin, Peter H.. (2012) Type 1 segmental Galli-Galli disease resulting from a previously unreported keratin 5 mutation. Journal of investigative dermatology, Vol. 132, H. 8. pp. 2100-2103.

2010

Has, Cristina and Burger, Bettina and Volz, A. and Kohlhase, Jürgen and Bruckner-Tuderman, Leena and Itin, Peter. (2010) Mild clinical phenotype of Kindler syndrome associated with late diagnosis and skin cancer. Dermatology (Basel, Switzerland), 221 (4). pp. 309-312.

This list was generated on Sun Sep 20 21:10:41 2020 CEST.