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JMIR Pediatrics and Parenting
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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 Sessions
Maia 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 V
Moira 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 Interpretation
Aurélie Ladang, Frank Rauch, Edgard Delvin, et al.
Calcified Tissue International
|
January 13, 2009
Intravenous pamidronate in osteogenesis imperfecta type VII
Moira 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 control
Bernd Schwahn, Frank Rauch, Udo Wendel, et al.
Journal of Pediatric Orthopedics
|
January 28, 2006
High prevalence of coxa vara in patients with severe osteogenesis imperfecta
Mehdi Aarabi, Frank Rauch, Reggie C Hamdy, et al.
Pediatric Endocrinology Reviews : PER
|
July 18, 2013
Osteogenesis imperfecta
Mouna 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 parameters
Thomas 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 variant
Kristiina Avela, Heljä Hirvinen, Mouna Ben Amor, et al.
Page
of 31
Search research articles
Search
Showing results (41-50 of 307) with videos related to
Sort By:
Page
of 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 Sessions
Maia 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 V
Moira 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 Interpretation
Aurélie Ladang, Frank Rauch, Edgard Delvin, et al.
Calcified Tissue International
|
January 13, 2009
Intravenous pamidronate in osteogenesis imperfecta type VII
Moira 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 control
Bernd Schwahn, Frank Rauch, Udo Wendel, et al.
Journal of Pediatric Orthopedics
|
January 28, 2006
High prevalence of coxa vara in patients with severe osteogenesis imperfecta
Mehdi Aarabi, Frank Rauch, Reggie C Hamdy, et al.
Pediatric Endocrinology Reviews : PER
|
July 18, 2013
Osteogenesis imperfecta
Mouna 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 parameters
Thomas 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 variant
Kristiina Avela, Heljä Hirvinen, Mouna Ben Amor, et al.
Page
of 31