8 Einträge gefunden

1. Relevant genetic variants are common in women with pregnancy and lactation-associated osteoporosis (PLO) and predispose to more severe clinical manifestations

   1. Butscheidt, Sebastian Karl
   2. Tsourdi, Elena
   3. Rolvien, Tim
   4. Delsmann, Alena
   5. Stürznickel, Julian
   6. Barvencik, Florian
   7. Jakob, Franz

   2021 - Forschungsinformationssystem des UKE - frei zugänglich
2. Clinical Phenotype and Relevance of LRP5 and LRP6 Variants in Patients With Early-Onset Osteoporosis (EOOP)

   1. Stürznickel, Julian
   2. Rolvien, Tim
   3. Delsmann, Alena
   4. Butscheidt, Sebastian
   5. Barvencik, Florian
   6. Mundlos, Stefan
   7. Schinke, Thorsten

   2021 - Forschungsinformationssystem des UKE - frei zugänglich
3. Skeletal deterioration in COL2A1-related spondyloepiphyseal dysplasia occurs prior to osteoarthritis

   1. Rolvien, Tim
   2. Yorgan, Timur Alexander
   3. Kornak, Uwe
   4. Hermans-Borgmeyer, Irm
   5. Mundlos, Stefan
   6. Schmidt, Tobias
   7. Niemeier, Andreas

   2020 - Forschungsinformationssystem des UKE
4. Loss of murine Gfi1 causes neutropenia and induces osteoporosis depending on the pathogen load and systemic inflammation

   1. Geissler, Sven
   2. Textor, Martin
   3. Stumpp, Sabine
   4. Seitz, Sebastian
   5. Lekaj, Anja
   6. Brunk, Sabrina
   7. Klaassen, Sabine

   2018 - Forschungsinformationssystem des UKE - frei zugänglich
5. Comparison of Bone Microarchitecture Between Adult Osteogenesis Imperfecta and Early-Onset Osteoporosis

   1. Rolvien, Tim
   2. Stürznickel, Julian
   3. Schmidt, Felix N
   4. Butscheidt, Sebastian
   5. Schmidt, Tobias
   6. Busse, Björn
   7. Mundlos, Stefan

   2018 - Forschungsinformationssystem des UKE
6. Deletions in PITX1 cause a spectrum of lower-limb malformations including mirror-image polydactyly.

   1. Klopocki, Eva
   2. Kähler, Christian
   3. Foulds, Nicola
   4. Shah, Hitesh
   5. Joseph, Benjamin
   6. Vogel, Hermann
   7. Lüttgen, Sabine

   2012 - Forschungsinformationssystem des UKE
7. Extensive molecular genetic analysis of the 3p14.3 region in patients with Zimmermann-Laband syndrome.

   1. Abo-Dalo, Benjamin
   2. Kim, Hyung-Goo
   3. Roes, Melanie
   4. Stefanova, Margarita
   5. Higgins, Anne
   6. Shen, Yiping
   7. Mundlos, Stefan

   2007 - Forschungsinformationssystem des UKE
8. Expansion of the genotypic and phenotypic spectrum in patients with KRAS germline mutations.

   1. Zenker, Martin
   2. Lehmann, Katarina
   3. Schulz, Anna Leana
   4. Barth, Helmut
   5. Hansmann, Dagmar
   6. Koenig, Rainer
   7. Korinthenberg, Rudolf

   2007 - Forschungsinformationssystem des UKE