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Medientyp
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Erscheinungsjahr
Autor/in
- Rolvien, Tim
- Amling, Michael 11
- Oheim, Ralf 8
- Kornak, Uwe 4
- Püschel, Klaus 4
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Sprache
16 Einträge gefunden
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Mice carrying a ubiquitous R235W mutation of Wnt1 display a bone-specific phenotype
- Yorgan, Timur
- Rolvien, Tim
- Stürznickel, Julian
- Vollersen, Nele
- Lange, Fabiola
- Zhao, Wenbo
- Baranowsky, Anke
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A novel, multi-level approach to assess allograft incorporation in revision total hip arthroplasty
- Rolvien, Tim
- Friesecke, Christian
- Butscheidt, Sebastian
- Gehrke, Thorsten
- Hahn, Michael
- Püschel, Klaus
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Long-term immobilization in elderly females causes a specific pattern of cortical bone and osteocyte deterioration different from postmenopausal osteoporosis
- Rolvien, Tim
- Milovanovic, Petar
- Schmidt, Felix N
- von Kroge, Simon
- Wölfel, Eva M
- Krause, Matthias
- Wulff, Birgit
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Primary intraosseous meningioma: clinical, histological, and differential diagnostic aspects
- Butscheidt, Sebastian
- Ernst, Marielle
- Rolvien, Tim
- Hubert, Jan
- Zustin, Jozef
- Amling, Michael
- Martens, Tobias
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Adult osteosclerotic metaphyseal dysplasia with progressive osteonecrosis of the jaws and abnormal bone resorption pattern due to a LRRK1 splice site mutation
- Howaldt, Antonia
- Hennig, Anna Floriane
- Rolvien, Tim
- Rössler, Uta
- Stelzer, Nina
- Knaus, Alexej
- Böttger, Sebastian
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Large osteocyte lacunae in iliac crest infantile bone are not associated with impaired mineral distribution or signs of osteocytic osteolysis
- Jandl, Nico Maximilian
- von Kroge, Simon
- Stürznickel, Julian
- Baranowsky, Anke
- Stockhausen, Kilian Elia
- Mushumba, Herbert
- Beil, Frank Timo
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Whole-Exome Sequencing Identifies Novel Compound Heterozygous ZNF469 Mutations in Two Siblings with Mild Brittle Cornea Syndrome
2020 - Forschungsinformationssystem des UKE -
A System to Determine Risk of Osteoporosis in Patients With Autoimmune Hepatitis
- Schmidt, Tobias
- Schmidt, Constantin
- Strahl, Andre
- Mussawy, Haider
- Rolvien, Tim
- Jandl, Nico M
- Casar, Christian
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Mice lacking plastin-3 display a specific defect of cortical bone acquisition
- Yorgan, Timur
- Sari, Hatice
- Rolvien, Tim
- Windhorst, Sabine
- Failla, Antonio Virgilio
- Kornak, Uwe
- Oheim, Ralf
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