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Zugriff
Einrichtung
Medientyp
- Text 7
Karte
Erscheinungsjahr
Autor/in
- Warnatz, Klaus
- Ammann, Sandra 2
- Ehl, Stephan 2
- Grimbacher, Bodo 2
- Heeg, Maximilian 2
- alle zeigen
Sprache
- Englisch 7
7 Einträge gefunden
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Therapeutic options for CTLA-4 Insufficiency
- Egg, David
- Rump, Ina Caroline
- Mitsuiki, Noriko
- Rojas-Restrepo, Jessica
- Maccari, Maria-Elena
- Schwab, Charlotte
- Gabrysch, Annemarie
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Establishing the Molecular Diagnoses in a Cohort of 291 Patients With Predominantly Antibody Deficiency by Targeted Next-Generation Sequencing: Experience From a Monocentric Study
- Rojas-Restrepo, Jessica
- Caballero-Oteyza, Andrés
- Huebscher, Katrin
- Haberstroh, Hanna
- Fliegauf, Manfred
- Keller, Baerbel
- Kobbe, Robin
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The German National Registry of Primary Immunodeficiencies (2012-2017)
- El-Helou, Sabine M
- Biegner, Anika-Kerstin
- Bode, Sebastian
- Ehl, Stephan R
- Heeg, Maximilian
- Maccari, Maria E
- Ritterbusch, Henrike
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Novel Patient with Late-Onset Familial Hemophagocytic Lymphohistiocytosis with STXBP2 Mutations Presenting with Autoimmune Hepatitis, Neurological Manifestations and Infections Associated with Hypogammaglobulinemia
- Esmaeilzadeh, Hossein
- Bemanian, Mohammad Hasan
- Nabavi, Mohammad
- Arshi, Saba
- Fallahpour, Morteza
- Fuchs, Ilka
- Zur Stadt, Udo
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Atypical familial hemophagocytic lymphohistiocytosis due to mutations in UNC13D and STXBP2 overlaps with primary immunodeficiency diseases
- Rohr, Jan
- Beutel, Karin
- Maul-Pavicic, Andrea
- Vraetz, Thomas
- Thiel, Jens
- Warnatz, Klaus
- Bondzio, Ilka