1. A Case of Muckle‐Wells Syndrome due to novel NLRP3 mutation. (29th August 2018) Authors: Yuksel, Simge; Metz, Martin; Lohse, Peter; Krause, Karoline Journal: Journal der Deutschen Dermatologischen Gesellschaft Issue: Volume 16:Number 10(2018) Page Start: 1250 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients. Issue 7 (1st July 2016) Authors: Sadovnick, A Dessa; Traboulsee, Anthony L; Bernales, Cecily Q; Ross, Jay P; Forwell, Amanda L; Yee, Irene M; Guillot-Noel, Lena; Fontaine, Bertrand; Cournu-Rebeix, Isabelle; Alcina, Antonio; Fedetz, Maria; Izquierdo, Guillermo; Matesanz, Fuencisla; Hilven, Kelly; Dubois, Bénédicte; Goris, An; Ast... Journal: G3 Issue: Volume 6:Issue 7(2016) Page Start: 2073 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Closing the case of APOE in multiple sclerosis: no association with disease risk in over 29 000 subjects. Issue 9 (11th September 2012) Authors: Lill, Christina M; Liu, Tian; Schjeide, Brit-Maren M; Roehr, Johannes T; Akkad, Denis A; Damotte, Vincent; Alcina, Antonio; Ortiz, Miguel A; Arroyo, Rafa; Lopez de Lapuente, Aitzkoa; Blaschke, Paul; Winkelmann, Alexander; Gerdes, Lisa-Ann; Luessi, Felix; Fernadez, Oscar; Izquierdo, Guillermo; Ant... Other Names: contributor. Journal: Journal of medical genetics Issue: Volume 49:Issue 9(2012) Page Start: 558 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Correlation of Secretory Activity of Neutrophils With Genotype in Patients With Familial Mediterranean Fever. Issue 12 (December 2016) Authors: Gohar, Faekah; Orak, Banu; Kallinich, Tilmann; Jeske, Marion; Lieber, Mareike; von Bernuth, Horst; Giese, Arnd; Weissbarth‐Riedel, Elisabeth; Haas, Johannes‐Peter; Dressler, Frank; Holzinger, Dirk; Lohse, Peter; Neudorf, Ulrich; Lainka, Elke; Hinze, Claas; Masjosthusmann, Katja; Kessel, Christoph... Journal: Arthritis & rheumatology Issue: Volume 68:Issue 12(2016) Page Start: 3010 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Early detection of sensorineural hearing loss in Muckle-Wells-syndrome. Issue 1 (December 2015) Authors: Kuemmerle-Deschner, Jasmin; Koitschev, Assen; Tyrrell, Pascal; Plontke, Stefan; Deschner, Norbert; Hansmann, Sandra; Ummenhofer, Katharina; Lohse, Peter; Koitschev, Christiane; Benseler, Susanne Journal: Pediatric rheumatology online journal Issue: Volume 13:Issue 1(2015) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Ein Fall von Muckle‐Wells‐Syndrom mit einer neuen NLRP3‐Mutation. (9th October 2018) Authors: Yuksel, Simge; Metz, Martin; Lohse, Peter; Krause, Karoline Journal: Journal der Deutschen Dermatologischen Gesellschaft Issue: Volume 16:Number 10(2018) Page Start: 1250 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Expanding spectrum of neurologic manifestations in patients with NLRP3 low-penetrance mutations. Issue 4 (August 2015) Authors: Schuh, Elisabeth; Lohse, Peter; Ertl-Wagner, Birgit; Witt, Matthias; Krumbholz, Markus; Frankenberger, Marion; Gerdes, Lisa-Ann; Hohlfeld, Reinhard; Kümpfel, Tania Journal: Neurology Issue: Volume 2:Issue 4(2015) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Fatal neonatal respiratory failure in an infant with congenital hypothyroidism due to haploinsufficiency of the NKX2-1 gene: alteration of pulmonary surfactant homeostasis. Issue 6 (28th June 2010) Authors: Kleinlein, Barbara; Griese, Matthias; Liebisch, Gerhard; Krude, Heiko; Lohse, Peter; Aslanidis, Charalampos; Schmitz, Gerd; Peters, Jochen; Holzinger, Andreas Journal: Archives of disease in childhood Issue: Volume 96:Issue 6(2011) Page Start: F453 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk. Issue 3 (12th January 2013) Authors: Lill, Christina M; Schjeide, Brit-Maren M; Graetz, Christiane; Liu, Tian; Damotte, Vincent; Akkad, Denis A; Blaschke, Paul; Gerdes, Lisa-Ann; Kroner, Antje; Luessi, Felix; Cournu-Rebeix, Isabelle; Hoffjan, Sabine; Winkelmann, Alexander; Touze, Emmanuel; Pico, Fernando; Corcia, Philippe; Otaegui, ... Journal: Journal of medical genetics Issue: Volume 50:Issue 3(2013) Page Start: 140 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Genome-wide significant association with seven novel multiple sclerosis risk loci. Issue 12 (16th October 2015) Authors: Lill, Christina M; Luessi, Felix; Alcina, Antonio; Sokolova, Ekaterina A; Ugidos, Nerea; de la Hera, Belén; Guillot-Noël, Léna; Malhotra, Sunny; Reinthaler, Eva; Schjeide, Brit-Maren M; Mescheriakova, Julia Y; Mashychev, Andriy; Wohlers, Inken; Akkad, Denis A; Aktas, Orhan; Alloza, Iraide; Antigü... Journal: Journal of medical genetics Issue: Volume 52:Issue 12(2015) Page Start: 848 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗