7 Einträge gefunden

1. Therapeutic options for CTLA-4 Insufficiency

   1. Egg, David
   2. Rump, Ina Caroline
   3. Mitsuiki, Noriko
   4. Rojas-Restrepo, Jessica
   5. Maccari, Maria-Elena
   6. Schwab, Charlotte
   7. Gabrysch, Annemarie

   2022 - Forschungsinformationssystem des UKE
2. Establishing the Molecular Diagnoses in a Cohort of 291 Patients With Predominantly Antibody Deficiency by Targeted Next-Generation Sequencing: Experience From a Monocentric Study

   1. Rojas-Restrepo, Jessica
   2. Caballero-Oteyza, Andrés
   3. Huebscher, Katrin
   4. Haberstroh, Hanna
   5. Fliegauf, Manfred
   6. Keller, Baerbel
   7. Kobbe, Robin

   2021 - Forschungsinformationssystem des UKE - frei zugänglich
3. Distinct molecular response patterns of activating STAT3 mutations associate with penetrance of lymphoproliferation and autoimmunity

   1. Jägle, Sabine
   2. Heeg, Maximilian
   3. Grün, Sarah
   4. Rensing-Ehl, Anne
   5. Maccari, Maria Elena
   6. Klemann, Christian
   7. Jones, Neil

   2020 - Forschungsinformationssystem des UKE
4. The German National Registry of Primary Immunodeficiencies (2012-2017)

   1. El-Helou, Sabine M
   2. Biegner, Anika-Kerstin
   3. Bode, Sebastian
   4. Ehl, Stephan R
   5. Heeg, Maximilian
   6. Maccari, Maria E
   7. Ritterbusch, Henrike

   2019 - Forschungsinformationssystem des UKE - frei zugänglich
5. Late-onset hemophagocytic lymphohistiocytosis (HLH) in an adult female with Griscelli syndrome type 2 (GS2)

   1. Henkes, Martin
   2. Finke, Jürgen
   3. Warnatz, Klaus
   4. Ammann, Sandra
   5. Stadt, Udo Zur
   6. Janka-Schaub, Gritta
   7. Brugger, Wolfram

   2015 - Forschungsinformationssystem des UKE
6. Novel Patient with Late-Onset Familial Hemophagocytic Lymphohistiocytosis with STXBP2 Mutations Presenting with Autoimmune Hepatitis, Neurological Manifestations and Infections Associated with Hypogammaglobulinemia

   1. Esmaeilzadeh, Hossein
   2. Bemanian, Mohammad Hasan
   3. Nabavi, Mohammad
   4. Arshi, Saba
   5. Fallahpour, Morteza
   6. Fuchs, Ilka
   7. Zur Stadt, Udo

   2015 - Forschungsinformationssystem des UKE
7. Atypical familial hemophagocytic lymphohistiocytosis due to mutations in UNC13D and STXBP2 overlaps with primary immunodeficiency diseases

   1. Rohr, Jan
   2. Beutel, Karin
   3. Maul-Pavicic, Andrea
   4. Vraetz, Thomas
   5. Thiel, Jens
   6. Warnatz, Klaus
   7. Bondzio, Ilka

   2010 - Forschungsinformationssystem des UKE - frei zugänglich