High risk of peri‐implant disease in periodontal Ehlers–Danlos Syndrome. A case series

por Rinner, Alexander, Zschocke, Johannes, Schossig, Anna, Gröbner, Rebekka, Strobl, Heinrich, Kapferer‐Seebacher, Ines
Publicado 2018

Array genotyping as diagnostic approach in medical genetics

por Witsch‐Baumgartner, Martina, Schwaninger, Gunda, Schnaiter, Simon, Kollmann, Franziska, Burkhard, Silja, Gröbner, Rebekka, Mühlegger, Beatrix, Schamschula, Esther, Kirchmeier, Peter, Zschocke, Johannes
Publicado 2022

Two Different Missense C1S Mutations, Associated to Periodontal Ehlers-Danlos Syndrome, Lead to Identical Molecular Outcomes

por Bally, Isabelle, Dalonneau, Fabien, Chouquet, Anne, Gröbner, Rebekka, Amberger, Albert, Kapferer-Seebacher, Ines, Stoiber, Heribert, Zschocke, Johannes, Thielens, Nicole M., Rossi, Véronique, Gaboriaud, Christine
Publicado 2019

C1R Mutations Trigger Constitutive Complement 1 Activation in Periodontal Ehlers-Danlos Syndrome

por Gröbner, Rebekka, Kapferer-Seebacher, Ines, Amberger, Albert, Redolfi, Rita, Dalonneau, Fabien, Björck, Erik, Milnes, Di, Bally, Isabelle, Rossi, Veronique, Thielens, Nicole, Stoiber, Heribert, Gaboriaud, Christine, Zschocke, Johannes
Publicado 2019

Corrigendum: C1R Mutations Trigger Constitutive Complement 1 Activation in Periodontal Ehlers-Danlos Syndrome

por Gröbner, Rebekka, Kapferer-Seebacher, Ines, Amberger, Albert, Redolfi, Rita, Dalonneau, Fabien, Björck, Erik, Milnes, Di, Bally, Isabelle, Rossi, Veronique, Thielens, Nicole, Stoiber, Heribert, Gaboriaud, Christine, Zschocke, Johannes
Publicado 2019

Oral characteristics in adult individuals with periodontal Ehlers‐Danlos syndrome

por Lepperdinger, Ulrike, Angwin, Chloe, Milnes, Di, Sobey, Glenda, Ghali, Neeti, Johnson, Diana, Brady, Angela F., Kammin, Tammy, Bowen, Jessica M., Gröbner, Rebekka, Lundberg, Pernilla, Scott, James, Zschocke, Johannes, van Dijk, Fleur S., Kapferer‐Seebacher, Ines
Publicado 2022