Julia Pagel

Familial Hemophagocytic Lymphohistiocytosis Type 5 (FHL-5) Is Caused by Mutations in Munc18-2 and Impaired Binding to Syntaxin 11

Udo zur Stadt, Jan Rohr, Wenke Seifert et al. · The American Journal of Human Genetics · 2009 · 411 citations · Full text

Impaired Binding, Mendelian Disorder, Autoimmune Disease +11

Distinct mutations in STXBP2 are associated with variable clinical presentations in patients with familial hemophagocytic lymphohistiocytosis type 5 (FHL5)

Julia Pagel, Karin Beutel, Kai Lehmberg et al. · Blood · 2012 · 162 citations · Full text

Atypical familial hemophagocytic lymphohistiocytosis due to mutations in UNC13D and STXBP2 overlaps with primary immunodeficiency diseases

Jan Rohr, Karin Beutel, Andrea Maul‐Pavicic et al. · Haematologica · 2010 · 127 citations · Full text

S100A8 and S100A9 Are Important for Postnatal Development of Gut Microbiota and Immune System in Mice and Infants

Maike Willers, Thomas Ulas, Lena Völlger et al. · Gastroenterology · 2020 · 127 citations · Full text

Gut Dysbiosis With Bacilli Dominance and Accumulation of Fermentation Products Precedes Late-onset Sepsis in Preterm Infants

Simon Graspeuntner, Silvio Waschina, Sven Künzel et al. · Clinical Infectious Diseases · 2018 · 98 citations · Full text