The brains of the bones: how osteocytes use WNT1 to control bone formation

بواسطة Rauch, Frank
الحاوية / القاعدة J Clin Invest (2017)

Abstracts of the 2017 International Workshop on Musculoskeletal and Neuronal Interactions

بواسطة Rauch, Frank
الحاوية / القاعدة J Musculoskelet Neuronal Interact (2017)

Role of Cartilage-associated Protein in Skeletal Development

بواسطة Morello, Roy, Rauch, Frank
الحاوية / القاعدة Curr Osteoporos Rep (2010)

Hypercalcemia and hypercalciuria during denosumab treatment in children with osteogenesis imperfecta type VI

بواسطة Trejo, Pamela, Rauch, Frank, Ward, Leanne
الحاوية / القاعدة J Musculoskelet Neuronal Interact (2018)

SAT-080 SLC29A3 Pathogenic Variant as a Causal for Dysosteosclerosis, a Poor Osteoclast Form of Osteopetrosis

بواسطة Seiltgens, Cristian, Rauch, Frank, Bardai, Ghalib
الحاوية / القاعدة J Endocr Soc (2020)

Giving Children With Osteogenesis Imperfecta a Voice: Participatory Approach for the Development of the Interactive Assessment and Communication Tool Sisom OI

بواسطة Siedlikowski, Maia, Rauch, Frank, Tsimicalis, Argerie
الحاوية / القاعدة J Med Internet Res (2020)

Osteogenesis Imperfecta: New Perspectives From Clinical and Translational Research

بواسطة Tauer, Josephine T, Robinson, Marie‐Eve, Rauch, Frank
الحاوية / القاعدة JBMR Plus (2019)

Does Sclerostin Depletion Stimulate Fracture Healing in a Mouse Model?

بواسطة Alzahrani, Mohammad M., Rauch, Frank, Hamdy, Reggie C.
الحاوية / القاعدة Clin Orthop Relat Res (2015)

The effects of intravenous pamidronate on the bone tissue of children and adolescents with osteogenesis imperfecta

بواسطة Rauch, Frank, Travers, Rose, Plotkin, Horacio, Glorieux, Francis H.
منشور في 2002

Genotype–phenotype correlations in nonlethal osteogenesis imperfecta caused by mutations in the helical domain of collagen type I

بواسطة Rauch, Frank, Lalic, Liljana, Roughley, Peter, Glorieux, Francis H
منشور في 2010

Genotype-Phenotype Correlations in Autosomal Dominant Osteogenesis Imperfecta

بواسطة Ben Amor, I. Mouna, Glorieux, Francis H., Rauch, Frank
منشور في 2011

Impact of three genetic musculoskeletal diseases: a comparative synthesis of achondroplasia, Duchenne muscular dystrophy and osteogenesis imperfecta

بواسطة Dogba, Maman Joyce, Rauch, Frank, Douglas, Erin, Bedos, Christophe
الحاوية / القاعدة Health Qual Life Outcomes (2014)

Fassier–Duval femoral rodding in children with osteogenesis imperfecta receiving bisphosphonates: functional outcomes at one year

بواسطة Ruck, Joanne, Dahan-Oliel, Noémi, Montpetit, Kathleen, Rauch, Frank, Fassier, François
منشور في 2011

Calvaria Bone Transcriptome in Mouse Models of Osteogenesis Imperfecta

بواسطة Moffatt, Pierre, Boraschi-Diaz, Iris, Marulanda, Juliana, Bardai, Ghalib, Rauch, Frank
الحاوية / القاعدة Int J Mol Sci (2021)

Androgen Ablation Leads to an Upregulation and Intranuclear Accumulation of Deoxyribonuclease I in Rat Prostate Epithelial Cells Paralleling Their Apoptotic Elimination

بواسطة Rauch, Frank, Polzar, Bernhard, Stephan, Harald, Zanotti, Silvia, Paddenberg, Renate, Mannherz, Hans Georg
منشور في 1997

Hip Dysplasia in Children With Osteogenesis Imperfecta: Association With Collagen Type I C-Propeptide Mutations

بواسطة Kishta, Waleed, Abduljabbar, Fahad H., Gdalevitch, Marie, Rauch, Frank, Hamdy, Reggie, Fassier, François
الحاوية / القاعدة J Pediatr Orthop (2017)

Dental and craniofacial characteristics caused by the p.Ser40Leu mutation in IFITM5

بواسطة Dagdeviren, Didem, Tamimi, Faleh, Lee, Brendan, Sutton, Reid, Rauch, Frank, Retrouvey, Jean-Marc
الحاوية / القاعدة Am J Med Genet A (2018)

Cone‐Beam Computed Tomography of Osteogenesis Imperfecta Types III and IV: Three‐Dimensional Evaluation of Craniofacial Features and Upper Airways

بواسطة Reznikov, Natalie, Dagdeviren, Didem, Tamimi, Faleh, Glorieux, Francis, Rauch, Frank, Retrouvey, Jean‐Marc
الحاوية / القاعدة JBMR Plus (2019)

From pediatric to adult care: strategic evaluation of a transition program for patients with osteogenesis imperfecta

بواسطة Dogba, Maman Joyce, Rauch, Frank, Wong, Trudy, Ruck, Joanne, Glorieux, Francis H, Bedos, Christophe
الحاوية / القاعدة BMC Health Serv Res (2014)

Spondyloepimetaphysial Dysplasia with Joint Laxity in Three Siblings with B3GALT6 Mutations

بواسطة Trejo, Pamela, Rauch, Frank, Glorieux, Francis H., Ouellet, Jean, Benaroch, Thierry, Campeau, Philippe M.
الحاوية / القاعدة Mol Syndromol (2017)