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Journal of Multidisciplinary Healthcare|January 30, 2023
Development of a Multidisciplinary Clinic for Patients with Ehlers Danlos Syndromes: Considerations and StrategiesWilliam R Black, Jordan T Jones, Eric T Rush, et al.
Molecular Genetics and Metabolism|February 21, 2025
Genetic characterization of a large cohort of individuals with a clinical suspicion of hypophosphatasia in the United StatesEric T Rush, Guillermo Del Angel, Juan Dong, et al.
Journal of Pediatric Orthopedics|July 6, 2016
Mid-term Results of Femoral and Tibial Osteotomies and Fassier-Duval Nailing in Children With Osteogenesis ImperfectaKhalid A Azzam, Eric T Rush, Bridget R Burke, et al.
SAGE Open Medicine|January 5, 2023
Gender dysphoria in adolescents with Ehlers-Danlos syndromeJordan T Jones, William R Black, Christine N Moser, et al.
Journal of Pediatric Genetics|September 15, 2016
Osteogenesis imperfecta caused by PPIB mutation with severe phenotype and congenital hearing lossEric T Rush, Kathleen S Caldwell, Rose M Kreikemeier, et al.
Cold Spring Harbor Molecular Case Studies|August 7, 2021
A novel likely pathogenic variant in a patient with Hermansky-Pudlak syndromeLisa A Lansdon, Dong Chen, Eric T Rush, et al.
Journal of Pediatric Orthopedics|September 24, 2016
Initial Experience With Percutaneous IM Rodding of the Humeri in Children With Osteogenesis ImperfectaLeonid S Grossman, Amber L Price, Eric T Rush, et al.
Heart (British Cardiac Society)|September 21, 2016
Echocardiographic phenotype in osteogenesis imperfecta varies with disease severityEric T Rush, Ling Li, Jennifer L Goodwin, et al.
The Journal of Clinical Endocrinology and Metabolism|July 14, 2016
Jansen Metaphyseal Chondrodysplasia due to Heterozygous H223R-PTH1R Mutations With or Without Overt HypercalcemiaSheela Nampoothiri, Eduardo Fernández-Rebollo, Dhanya Yesodharan, et al.
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