Facetten
Zugriff
Einrichtung
Medientyp
- Text 6
Karte
Erscheinungsjahr
Autor/in
- Kornak, Uwe
- Stürznickel, Julian
- Amling, Michael 5
- Oheim, Ralf 4
- Delsmann, Alena 3
- alle zeigen
Sprache
- Englisch 6
6 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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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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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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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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