Search

Author/Creator Luksch, Hella

1. Juvenile arthritis caused by a novel FAMIN (LACC1) mutation in two children with systemic and extended oligoarticular course. Issue 1 (December 2016)

Authors:
Kallinich, Tilmann; Thorwarth, Anne; von Stuckrad, Sae-Lim; Rösen-Wolff, Angela; Luksch, Hella; Hundsdoerfer, Patrick; Minden, Kirsten; Krawitz, Peter
Journal:
Pediatric rheumatology online journal
Issue:
Volume 14:Issue 1(2016)
Page Start:
1
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. Naturally Occurring Genetic Variants of Human Caspase‐1 Differ Considerably in Structure and the Ability to Activate Interleukin‐1β. Issue 1 (10th August 2012)

Authors:
Luksch, Hella; Romanowski, Michael J.; Chara, Osvaldo; Tüngler, Victoria; Caffarena, Ernesto R.; Heymann, Michael C.; Lohse, Peter; Aksentijevich, Ivona; Remmers, Elaine F.; Flecks, Silvana; Quoos, Nadine; Gramatté, Johannes; Petzold, Cathleen; Hofmann, Sigrun R.; Winkler, Stefan; Pessler, Frank;...
Journal:
Human mutation
Issue:
Volume 34:Issue 1(2013:Jan.)
Page Start:
122
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. SAMHD1 prevents autoimmunity by maintaining genome stability. Issue 3 (20th January 2014)

Authors:
Kretschmer, Stefanie; Wolf, Christine; König, Nadja; Staroske, Wolfgang; Guck, Jochen; Häusler, Martin; Luksch, Hella; Nguyen, Laura A; Kim, Baek; Alexopoulou, Dimitra; Dahl, Andreas; Rapp, Alexander; Cardoso, M Cristina; Shevchenko, Anna; Lee-Kirsch, Min Ae
Journal:
Annals of the rheumatic diseases
Issue:
Volume 74:Issue 3(2015)
Page Start:
e17
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗