P02-030 - Unusual CNS manifestation

por Schuh, E, Lohse, P, Meinl, I, Kümpfel, T
Publicado 2013

PW02-032 - CNS manifestations and NLRP3/CIAS1 gene mutations

por Kümpfel, T, Schuh, E, Hohlfeld, R, Lohse, P
Publicado 2013

PW02-033 - Cytokine profile in CSF in CAPS patients

por Schuh, E, Lohse, P, Frankenberger, M, Meinl, I, Kuempfel, T
Publicado 2013

PW03-029 – Risk factors for AA-type amyloidosis in Germany

por Blank, N, Lohse, P, Hegenbart, U, Lorenz, H-M, Schoenland, SO
Publicado 2013

Neurological manifestations in autoinflammatory syndromes: a series of 131 patients from our neuroimmunology departement

por Schuh, E, Lohse, P, Havla, J, Meinl, I, Gerdes, L-A, Hohlfeld, R, Kümpfel, T
Publicado 2015

Severe macrophage activation syndrome. Is there a causative role for a homozygous A91V mutation in the perforin gene?

por Girschick, H, Rossi, R, Kölsch, U, Ammann, S, Lohse, P, Morbach, H, von Bernuth, H, Ehl, S
Publicado 2015

PReS-FINAL-2215: Genotype-phenotype correlations in children with Familial Mediterranean Fever in Germany

por Gohar, F, Jeske, M, Lohse, P, Kallinich, T, Neudorf, U, Niehues, T, Wittkowski, H, Lainka, E, Foell, D
Publicado 2013

PW02-040 - Low-penetrance NLRP3 variants

por Endres, T, Hofer, F, Goldbach-Mansky, R, Hoffman, HM, Blank, N, Krause, K, Rietschel, C, Horneff, G, Lohse, P, Kuemmerle-Deschner, J
Publicado 2013

PReS-FINAL-2331: Low-penetrance NLRP3 variants

por Endres, T, Hofer, F, Goldbach-Mansky, R, Hoffman, HM, Blank, N, Krause, K, Rietschel, C, Horneff, G, Lohse, P, Kuemmerle-Deschner, J
Publicado 2013

A novel mutatioin in the PSTPIP1 gene is associated with an autoinflammatory disease distinct from classical PAPA syndrome

por Holzinger, D, Austermann, J, Lohse, P, Aksentijevich, I, Holland, S, Gattorno, M, Rodríguez-Gallego, C, Fessatou, S, Isidor, B, Tokio, S, Bernstein, J, Sampson, B, Sunderkoetter, C, Roth, J
Publicado 2011

P01-008 – FMF genotype-phenotype correlations in Germany

por Jeske, M, Lohse, P, Kallinich, T, Berger, T, Rietschel, C, Holzinger, D, Kamlah, C, Lankisch, P, Berendes, R, Dückers, G, Horneff, G, Lilienthal, E, Haas, JP, Giese, A, Dressler, F, Berrang, J, Pütter, C, Braunewell, L, Neudorf, U, Niehues, T, Lainka, E
Publicado 2013

PW02-018 - Impact of PSTPIP1 mutaions on clinical phenotype

por Holzinger, D, Lohse, P, Faßl, S, Austermann, J, Vogl, T, de Jager, W, Holland, S, Gattorno, M, Rodriguez-Gallego, C, Arostegui, J, Fessatou, S, Isidor, B, Ito, K, Epple, H-J, Bernstein, J, Jeng, M, Lionetti, G, Ong, P, Hinze, C, Sampson, B, Sunderkoetter, C, Foell, D, Chae, J, Ombrello, A, Brady, J, Aksentijevich, I, Roth, J
Publicado 2013