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Einrichtung
Medientyp
- Text 11
Karte
Erscheinungsjahr
Autor/in
- Amling, Michael
- Kornak, Uwe
- Oheim, Ralf 10
- Rolvien, Tim 8
- Schinke, Thorsten 8
- alle zeigen
Sprache
- Englisch 11
11 Einträge gefunden
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Clinical spectrum of Hereditary Hypophosphatemic rickets with Hypercalciuria (HHRH)
- Stürznickel, Julian
- Heider, Fiona
- Delsmann, Alena
- Gödel, Markus
- Grünhagen, Johannes
- Huber, Tobias B
- Kornak, Uwe
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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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Compound heterozygous frameshift mutations in MESD cause a lethal syndrome suggestive of osteogenesis imperfecta type XX
- Stürznickel, Julian
- Jähn-Rickert, Katharina
- Zustin, Jozef
- Hennig, Floriane
- Delsmann, Maximilian M
- Schoner, Katharina
- Rehder, Helga
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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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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