Facetten
Zugriff
Einrichtung
Medientyp
- Text 9
Karte
Erscheinungsjahr
Autor/in
- Amling, Michael
- Oheim, Ralf
- Rolvien, Tim 8
- Kornak, Uwe 5
- Schinke, Thorsten 4
- alle zeigen
Sprache
- Englisch 9
9 Einträge gefunden
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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 -
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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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Human Heterozygous ENPP1 Deficiency Is Associated With Early Onset Osteoporosis, a Phenotype Recapitulated in a Mouse Model of Enpp1 Deficiency
- Oheim, Ralf
- Zimmerman, Kristin
- Maulding, Nathan D
- Stürznickel, Julian
- von Kroge, Simon
- Kavanagh, Dillon
- Stabach, Paul R
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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