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Osteogenesis imperfecta

Pleiotropic effects of a recessive Col1a2 mutation occurring in a mouse model of severe osteogenesis imperfecta

Michelangelo Corcelli, Rachel Sagar, [ ... ], Pascale V. Guillot

Association of trabecular bone score and bone mineral apparent density with the severity of bone fragility in children and adolescents with osteogenesis imperfecta: A cross-sectional study

Yasuhisa Ohata, Taichi Kitaoka, [ ... ], Keiichi Ozono

Morphological and mechanical characterization of bone phenotypes in the Amish G610C murine model of osteogenesis imperfecta

Rachel Kohler, Carli A. Tastad, Amy Creecy, Joseph M. Wallace

Upper extremity prosthetic selection influences loading of transhumeral osseointegrated systems

Carolyn E. Taylor, Alex J. Drew, [ ... ], Heath B. Henninger

Variation in bone response to the placement of percutaneous osseointegrated endoprostheses: A 24-month follow-up in sheep

Sujee Jeyapalina, James Peter Beck, [ ... ], Kent N. Bachus

Substitutions for arginine at position 780 in triple helical domain of the α1(I) chain alter folding of the type I procollagen molecule and cause osteogenesis imperfecta

Elena Makareeva, Guoli Sun, [ ... ], Sergey Leikin

The osteogenic cell surface marker BRIL/IFITM5 is dispensable for bone development and homeostasis in mice

Alexa Patoine, Abdallah Husseini, [ ... ], Pierre Moffatt

Mutations in COL1A1 and COL1A2 and dental aberrations in children and adolescents with osteogenesis imperfecta – A retrospective cohort study

Kristofer Andersson, Göran Dahllöf, [ ... ], Barbro Malmgren

Multiparametric Classification of Skin from Osteogenesis Imperfecta Patients and Controls by Quantitative Magnetic Resonance Microimaging

Beth G. Ashinsky, Kenneth W. Fishbein, [ ... ], Richard G. Spencer

Involving Families with Osteogenesis Imperfecta in Health Service Research: Joint Development of the OI/ECE Questionnaire

Maman Joyce Dogba, Noémi Dahan-Oliel, [ ... ], Frank Rauch

Development of a High-Throughput Resequencing Array for the Detection of Pathogenic Mutations in Osteogenesis Imperfecta

Yao Wang, Yazhou Cui, Xiaoyan Zhou, Jinxiang Han

Novel Mutations in FKBP10 and PLOD2 Cause Rare Bruck Syndrome in Chinese Patients

Peiran Zhou, Yi Liu, [ ... ], Mei Li

Phenotype and Genotype Analysis of Chinese Patients with Osteogenesis Imperfecta Type V

Zeng Zhang, Mei Li, [ ... ], Zhen-Lin Zhang

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