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Frank Rauch

Showing results (41-50 of 307) with videos related to

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JMIR Pediatrics and Parenting|August 12, 2021
Experiences of Children With Osteogenesis Imperfecta in the Co-design of the Interactive Assessment and Communication Tool Sisom OI: Secondary Analysis of Qualitative Design SessionsMaia Siedlikowski, Lianna Curiale, Frank Rauch, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 25, 2007
Natural history of hyperplastic callus formation in osteogenesis imperfecta type VMoira S Cheung, Francis H Glorieux, Frank Rauch
Clinical Orthopaedics and Related Research|November 27, 2015
Does Sclerostin Depletion Stimulate Fracture Healing in a Mouse Model?Mohammad M Alzahrani, Frank Rauch, Reggie C Hamdy
Calcified Tissue International|March 4, 2022
Bone Turnover Markers in Children: From Laboratory Challenges to Clinical InterpretationAurélie Ladang, Frank Rauch, Edgard Delvin, et al.
Calcified Tissue International|January 13, 2009
Intravenous pamidronate in osteogenesis imperfecta type VIIMoira S Cheung, Francis H Glorieux, Frank Rauch
The Journal of Pediatrics|September 10, 2002
Low bone mass in glycogen storage disease type 1 is associated with reduced muscle force and poor metabolic controlBernd Schwahn, Frank Rauch, Udo Wendel, et al.
Journal of Pediatric Orthopedics|January 28, 2006
High prevalence of coxa vara in patients with severe osteogenesis imperfectaMehdi Aarabi, Frank Rauch, Reggie C Hamdy, et al.
Pediatric Endocrinology Reviews : PER|July 18, 2013
Osteogenesis imperfectaMouna Ben Amor, Frank Rauch, Elena Monti, et al.
The Journal of Clinical Endocrinology and Metabolism|February 10, 2012
Serum 24,25-dihydroxyvitamin D concentrations in osteogenesis imperfecta: relationship to bone parametersThomas Edouard, Abdallah Husseini, Francis H Glorieux, et al.
European Journal of Medical Genetics|October 15, 2014
Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly in a Finnish woman: first confirmation of a duplication in RUNX2 as pathogenic variantKristiina Avela, Heljä Hirvinen, Mouna Ben Amor, et al.
Pageof 31

Showing results (41-50 of 307) with videos related to

Sort By:
Pageof 31
JMIR Pediatrics and Parenting|August 12, 2021
Experiences of Children With Osteogenesis Imperfecta in the Co-design of the Interactive Assessment and Communication Tool Sisom OI: Secondary Analysis of Qualitative Design SessionsMaia Siedlikowski, Lianna Curiale, Frank Rauch, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 25, 2007
Natural history of hyperplastic callus formation in osteogenesis imperfecta type VMoira S Cheung, Francis H Glorieux, Frank Rauch
Clinical Orthopaedics and Related Research|November 27, 2015
Does Sclerostin Depletion Stimulate Fracture Healing in a Mouse Model?Mohammad M Alzahrani, Frank Rauch, Reggie C Hamdy
Calcified Tissue International|March 4, 2022
Bone Turnover Markers in Children: From Laboratory Challenges to Clinical InterpretationAurélie Ladang, Frank Rauch, Edgard Delvin, et al.
Calcified Tissue International|January 13, 2009
Intravenous pamidronate in osteogenesis imperfecta type VIIMoira S Cheung, Francis H Glorieux, Frank Rauch
The Journal of Pediatrics|September 10, 2002
Low bone mass in glycogen storage disease type 1 is associated with reduced muscle force and poor metabolic controlBernd Schwahn, Frank Rauch, Udo Wendel, et al.
Journal of Pediatric Orthopedics|January 28, 2006
High prevalence of coxa vara in patients with severe osteogenesis imperfectaMehdi Aarabi, Frank Rauch, Reggie C Hamdy, et al.
Pediatric Endocrinology Reviews : PER|July 18, 2013
Osteogenesis imperfectaMouna Ben Amor, Frank Rauch, Elena Monti, et al.
The Journal of Clinical Endocrinology and Metabolism|February 10, 2012
Serum 24,25-dihydroxyvitamin D concentrations in osteogenesis imperfecta: relationship to bone parametersThomas Edouard, Abdallah Husseini, Francis H Glorieux, et al.
European Journal of Medical Genetics|October 15, 2014
Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly in a Finnish woman: first confirmation of a duplication in RUNX2 as pathogenic variantKristiina Avela, Heljä Hirvinen, Mouna Ben Amor, et al.
Pageof 31