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- Oheim, Ralf
- Amling, Michael 37
- Rolvien, Tim 28
- Barvencik, Florian 18
- Schinke, Thorsten 13
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48 Einträge gefunden
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Bone mineral density and microarchitecture change during skeletal growth in harbor seals (Phoca vitulina) from the German coast
2023 - Forschungsinformationssystem des UKE - frei zugänglich -
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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Beneficial effects of denosumab on muscle performance in patients with low BMD: a retrospective, propensity score-matched study
- Rupp, Tobias
- von Vopelius, Emil
- Strahl, André
- Oheim, Ralf
- Barvencik, Florian
- Amling, Michael
- Rolvien, Tim
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Blast injury on harbour porpoises (Phocoena phocoena) from the Baltic Sea after explosions of deposits of World War II ammunition
- Siebert, Ursula
- Stürznickel, Julian
- Schaffeld, Tobias
- Oheim, Ralf
- Rolvien, Tim
- Prenger-Berninghoff, Ellen
- Wohlsein, Peter
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Genetic Diagnostics in Routine Osteological Assessment of Adult Low Bone Mass Disorders
- Oheim, Ralf
- Tsourdi, Elena
- Seefried, Lothar
- Beller, Gisela
- Schubach, Max
- Vettorazzi, Eik
- Stürznickel, Julian
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Characterization of hearing-impairment in Generalized Arterial Calcification of Infancy (GACI)
- Theng, Elizabeth H
- Brewer, Carmen C
- Oheim, Ralf
- Zalewski, Christopher K
- King, Kelly A
- Delsmann, Maximillian M
- Rolvien, Tim
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Tumor localization and treatment of tumor-induced osteomalacia, Tumorlokalisation und Therapie der onkogenen Osteomalazie
2022 - Forschungsinformationssystem des UKE -
Bone healing and reactivation of remodeling under asfotase alfa therapy in adult patients with pediatric-onset hypophosphatasia
- Stürznickel, Julian
- Schmidt, Felix N
- von Vopelius, Emil
- Delsmann, Maximilian M
- Schmidt, Constantin
- Jandl, Nico Maximilian
- Oheim, Ralf
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Clinical and Radiological Characterization of Patients with Immobilizing and Progressive Stress Fractures in Methotrexate Osteopathy
- Rolvien, Tim
- Jandl, Nico Maximilian
- Stürznickel, Julian
- Beil, Frank Timo
- Kötter, Ina
- Oheim, Ralf
- Lohse, Ansgar W
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Autosomal recessive hypophosphatemic rickets type 2 (ARHR2) due to ENPP1-deficiency
2021 - Forschungsinformationssystem des UKE - frei zugänglich -
Conductive hearing loss in the Hyp mouse model of X-linked hypophosphatemia is accompanied by hypomineralization of the auditory ossicles
- Delsmann, Maximilian M
- Seist, Richard
- Stürznickel, Julian
- Schmidt, Felix N
- Mansour, Amer
- Kobelski, Margaret M
- Broocks, Gabriel
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Bilateral Looser zones or pseudofractures in the anteromedial tibia as a component of medial tibial stress syndrome in athletes
- Stürznickel, Julian
- Jandl, Nico Maximilian
- Delsmann, Maximilian M
- von Vopelius, Emil
- Barvencik, Florian
- Amling, Michael
- Ueblacker, Peter
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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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Response of the ENPP1-deficient skeletal phenotype to oral phosphate supplementation and/or enzyme replacement therapy: Comparative studies in Humans and Mice
- Ferreira, Carlos R
- Kavanagh, Dillon
- Oheim, Ralf
- Zimmerman, Kristin
- Stürznickel, Julian
- Li, Xiaofeng
- Stabach, Paul
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Challenges in the management of tumor-induced osteomalacia (TIO)
- Brandi, Maria Luisa
- Clunie, Gavin P R
- Houillier, Pascal
- Jan de Beur, Suzanne M
- Minisola, Salvatore
- Oheim, Ralf
- Seefried, Lothar
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Bone microarchitecture in patients with autoimmune hepatitis
- Schmidt, Constantin
- Stürznickel, Julian
- Strahl, André
- Oheim, Ralf
- Weiler-Normann, Christina
- Sebode, Marcial
- Barvencik, Florian
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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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Whole-Exome Sequencing Identifies Novel Compound Heterozygous ZNF469 Mutations in Two Siblings with Mild Brittle Cornea Syndrome
2020 - Forschungsinformationssystem des UKE -