Facetten
Zugriff
Einrichtung
Medientyp
- Text 9
Karte
Erscheinungsjahr
Autor/in
- Kornak, Uwe
- Rolvien, Tim
- Amling, Michael 8
- Oheim, Ralf 8
- Schinke, Thorsten 7
- alle zeigen
Sprache
- Englisch 9
9 Einträge gefunden
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Clinical Phenotype and Relevance of LRP5 and LRP6 Variants in Patients With Early-Onset Osteoporosis (EOOP)
- Stürznickel, Julian
- Rolvien, Tim
- Delsmann, Alena
- Butscheidt, Sebastian
- Barvencik, Florian
- Mundlos, Stefan
- Schinke, Thorsten
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Relevant genetic variants are common in women with pregnancy and lactation-associated osteoporosis (PLO) and predispose to more severe clinical manifestations
- Butscheidt, Sebastian Karl
- Tsourdi, Elena
- Rolvien, Tim
- Delsmann, Alena
- Stürznickel, Julian
- Barvencik, Florian
- Jakob, Franz
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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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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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Clinical Significance of DXA and HR-pQCT in Autosomal Dominant Osteopetrosis (ADO II)
- Butscheidt, Sebastian
- Rolvien, Tim
- Kornak, Uwe
- Schmidt, Felix N
- Schinke, Thorsten
- Amling, Michael
- Oheim, Ralf
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A Novel ANO5 Mutation Causing Gnathodiaphyseal Dysplasia With High Bone Turnover Osteosclerosis
- Rolvien, Tim
- Koehne, Till
- Kornak, Uwe
- Lehmann, Wolfgang
- Amling, Michael
- Schinke, Thorsten
- Oheim, Ralf