Crigler-Najjar syndrome type 2: Novel UGT1A1 mutation

by Nair, Karippoth Mohandas, Lohse, Peter, Nampoothiri, Sheela
Published 2012

GCK-MODY (MODY 2) Caused by a Novel p.Phe330Ser Mutation

by Bonfig, Walter, Hermanns, Sandra, Warncke, Katharina, Eder, Gabriele, Engelsberger, Ilse, Burdach, Stefan, Ziegler, Annette Gabriele, Lohse, Peter
Published 2011

Peripheral Hole Acceptor Moieties on an Organic Dye Improve Dye‐Sensitized Solar Cell Performance

by Hao, Yan, Gabrielsson, Erik, Lohse, Peter William, Yang, Wenxing, Johansson, Erik M. J., Hagfeldt, Anders, Sun, Licheng, Boschloo, Gerrit
Published 2015

Expanding spectrum of neurologic manifestations in patients with NLRP3 low-penetrance mutations

by Schuh, Elisabeth, Lohse, Peter, Ertl-Wagner, Birgit, Witt, Matthias, Krumbholz, Markus, Frankenberger, Marion, Gerdes, Lisa-Ann, Hohlfeld, Reinhard, Kümpfel, Tania
Published 2015

Multiple sclerosis–like lesions and type I interferon signature in a patient with RVCL

by Schuh, Elisabeth, Ertl-Wagner, Birgit, Lohse, Peter, Wolf, Waltraud, Mann, Johannes F., Lee-Kirsch, Min Ae, Hohlfeld, Reinhard, Kümpfel, Tania
Published 2014

Genetic variants of adiponectin receptor 2 are associated with increased adiponectin levels and decreased triglyceride/VLDL levels in patients with metabolic syndrome

by Broedl, Uli C, Lehrke, Michael, Fleischer-Brielmaier, Elisabeth, Tietz, Anne B, Nagel, Jutta M, Göke, Burkhard, Lohse, Peter, Parhofer, Klaus G
Published 2006

NLRP3 E311K mutation in a large family with Muckle-Wells syndrome - description of a heterogeneous phenotype and response to treatment

by Kuemmerle-Deschner, Jasmin B, Lohse, Peter, Koetter, Ina, Dannecker, Guenther E, Reess, Fabian, Ummenhofer, Katharina, Koch, Silvia, Tzaribachev, Nikolay, Bialkowski, Anja, Benseler, Susanne M
Published 2011

Early detection of sensorineural hearing loss in Muckle-Wells-syndrome

by Kuemmerle-Deschner, Jasmin B., Koitschev, Assen, Tyrrell, Pascal N., Plontke, Stefan K., Deschner, Norbert, Hansmann, Sandra, Ummenhofer, Katharina, Lohse, Peter, Koitschev, Christiane, Benseler, Susanne M.
Published 2015

The NOD2 Single Nucleotide Polymorphism rs72796353 (IVS4+10 A>C) Is a Predictor for Perianal Fistulas in Patients with Crohn's Disease in the Absence of Other NOD2 Mutations

by Schnitzler, Fabian, Friedrich, Matthias, Wolf, Christiane, Stallhofer, Johannes, Angelberger, Marianne, Diegelmann, Julia, Olszak, Torsten, Tillack, Cornelia, Beigel, Florian, Göke, Burkhard, Glas, Jürgen, Lohse, Peter, Brand, Stephan
Published 2015

The NOD2 p.Leu1007fsX1008 Mutation (rs2066847) Is a Stronger Predictor of the Clinical Course of Crohn's Disease than the FOXO3A Intron Variant rs12212067

by Schnitzler, Fabian, Friedrich, Matthias, Wolf, Christiane, Angelberger, Marianne, Diegelmann, Julia, Olszak, Torsten, Beigel, Florian, Tillack, Cornelia, Stallhofer, Johannes, Göke, Burkhard, Glas, Jürgen, Lohse, Peter, Brand, Stephan
Published 2014

CEACAM6 Gene Variants in Inflammatory Bowel Disease

by Glas, Jürgen, Seiderer, Julia, Fries, Christoph, Tillack, Cornelia, Pfennig, Simone, Weidinger, Maria, Beigel, Florian, Olszak, Torsten, Lass, Ulrich, Göke, Burkhard, Ochsenkühn, Thomas, Wolf, Christiane, Lohse, Peter, Müller-Myhsok, Bertram, Diegelmann, Julia, Czamara, Darina, Brand, Stephan
Published 2011

Long-term follow-up and treatment of congenital alveolar proteinosis

by Griese, Matthias, Ripper, Jan, Sibbersen, Anke, Lohse, Pia, Lohse, Peter, Brasch, Frank, Schams, Andrea, Pamir, Asli, Schaub, Bianca, Muensterer, Oliver J, Schön, Carola, Glöckner-Pagel, Judith, Nicolai, Thomas, Reiter, Karl, Hector, Andreas
Published 2011

Involvement of the Same TNFR1 Residue in Mendelian and Multifactorial Inflammatory Disorders

by Jéru, Isabelle, Charmion, Serge, Cochet, Emmanuelle, Copin, Bruno, Duquesnoy, Philippe, Garcia, Maria Teresa Mitjavila, Le Borgne, Gaëlle, Cathebras, Pascal, Gaillat, Jacques, Karabina, Sonia, Dodé, Catherine, Lohse, Peter, Hentgen, Véronique, Amselem, Serge
Published 2013

Treatment of Muckle-Wells syndrome: analysis of two IL-1-blocking regimens

by Kuemmerle-Deschner, Jasmin B, Wittkowski, Helmut, Tyrrell, Pascal N, Koetter, Ina, Lohse, Peter, Ummenhofer, Katharina, Reess, Fabian, Hansmann, Sandra, Koitschev, Assen, Deuter, Christoph, Bialkowski, Anja, Foell, Dirk, Benseler, Susanne M
Published 2013

Categorizing diffuse parenchymal lung disease in children

by Griese, Matthias, Irnstetter, Armin, Hengst, Meike, Burmester, Helen, Nagel, Felicitas, Ripper, Jan, Feilcke, Maria, Pawlita, Ingo, Gothe, Florian, Kappler, Matthias, Schams, Andrea, Wesselak, Traudl, Rauch, Daniela, Wittmann, Thomas, Lohse, Peter, Brasch, Frank, Kröner, Carolin
Published 2015

Characterization of CSF2RA mutation related juvenile pulmonary alveolar proteinosis

by Hildebrandt, Jenna, Yalcin, Ebru, Bresser, Hans-Georg, Cinel, Guzin, Gappa, Monika, Haghighi, Alireza, Kiper, Nural, Khalilzadeh, Soheila, Reiter, Karl, Sayer, John, Schwerk, Nicolaus, Sibbersen, Anke, Van Daele, Sabine, Nübling, Georg, Lohse, Peter, Griese, Matthias
Published 2014

rs1004819 Is the Main Disease-Associated IL23R Variant in German Crohn's Disease Patients: Combined Analysis of IL23R, CARD15, and OCTN1/2 Variants

by Glas, Jürgen, Seiderer, Julia, Wetzke, Martin, Konrad, Astrid, Török, Helga-Paula, Schmechel, Silke, Tonenchi, Laurian, Grassl, Christine, Dambacher, Julia, Pfennig, Simone, Maier, Kerstin, Griga, Thomas, Klein, Wolfram, Epplen, Jörg T., Schiemann, Uwe, Folwaczny, Christian, Lohse, Peter, Göke, Burkhard, Ochsenkühn, Thomas, Müller-Myhsok, Bertram, Folwaczny, Matthias, Mussack, Thomas, Brand, Stephan
Published 2007

Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients

by 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, Astobiza, Ianire, Alloza, Iraide, Antigüedad, Alfredo, Vandenbroeck, Koen, Akkad, Denis A., Aktas, Orhan, Blaschke, Paul, Buttmann, Mathias, Chan, Andrew, Epplen, Joerg T., Gerdes, Lisa-Ann, Kroner, Antje, Kubisch, Christian, Kümpfel, Tania, Lohse, Peter, Rieckmann, Peter, Zettl, Uwe K., Zipp, Frauke, Bertram, Lars, Lill, Christina M, Fernandez, Oscar, Urbaneja, Patricia, Leyva, Laura, Alvarez-Cermeño, Jose Carlos, Arroyo, Rafael, Garagorri, Aroa M., García-Martínez, Angel, Villar, Luisa M., Urcelay, Elena, Malhotra, Sunny, Montalban, Xavier, Comabella, Manuel, Berger, Thomas, Fazekas, Franz, Reindl, Markus, Schmied, Mascha C., Zimprich, Alexander, Vilariño-Güell, Carles
Published 2016