Michael M. Schündeln

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 · 130 citations · Full text

Life Sciences, Hematology, Immunology +16

Incidence of second cancers after radiotherapy and systemic chemotherapy in heritable retinoblastoma survivors: A report from the German reference center

Petra Temming, Marina Arendt, Anja Viehmann et al. · Pediatric Blood & Cancer · 2016 · 128 citations

Medicine, Oncology, Radiation Oncology +15

Effects of RANK-Ligand Antibody (Denosumab) Treatment on Bone Turnover Markers in a Girl With Juvenile Paget's Disease

Corinna Grasemann, Michael M. Schündeln, M. Hövel et al. · The Journal of Clinical Endocrinology & Metabolism · 2013 · 100 citations · Full text

Medicine, Pediatrics, Bone Metabolism +16

A Piece of the Puzzle: The Bone Health Index of the BoneXpert Software Reflects Cortical Bone Mineral Density in Pediatric and Adolescent Patients

Michael M. Schündeln, Laura Marschke, Jens Bauer et al. · PLoS ONE · 2016 · 48 citations · Full text

Medicine, Radiology, Diagnostic Imaging +15

How Eye-Preserving Therapy Affects Long-Term Overall Survival in Heritable Retinoblastoma Survivors

Petra Temming, Marina Arendt, Anja Viehmann et al. · Journal of Clinical Oncology · 2016 · 48 citations

Medicine, Oncology, Ophthalmology +14