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Francis Glorieux

Showing results (1-10 of 11) with videos related to

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Pediatric Endocrinology Reviews : PER|July 18, 2013
Emerging concepts in pediatric bone diseaseFrancis Glorieux
Bulletin De L'Academie Nationale De Medecine|July 31, 2002
[Vitamin D and pregnancy]Bernard-Louis Salle, Edgar Delvin, Francis Glorieux
Pediatrics|February 4, 2003
Safety profile of frequent short courses of oral glucocorticoids in acute pediatric asthma: impact on bone metabolism, bone density, and adrenal functionFrancine M Ducharme, Gilles Chabot, Constantin Polychronakos, et al.
JBMR Plus|July 27, 2019
Cone-Beam Computed Tomography of Osteogenesis Imperfecta Types III and IV: Three-Dimensional Evaluation of Craniofacial Features and Upper AirwaysNatalie Reznikov, Didem Dagdeviren, Faleh Tamimi, et al.
Journal of Pediatric Rehabilitation Medicine|July 16, 2011
Activities and participation in young adults with osteogenesis imperfectaKathleen Montpetit, Noémi Dahan-Oliel, Joanne Ruck-Gibis, et al.
Bone|July 31, 2020
Assessment of longitudinal bone growth in osteogenesis imperfecta using metacarpophalangeal pattern profilesDamian Rauch, Marie-Eve Robinson, Cristian Seiltgens, et al.
Bone|August 15, 2022
Craniofacial and dental phenotype of two girls with osteogenesis imperfecta due to mutations in CRTAPJuliana Marulanda, Karissa Ludwig, Francis Glorieux, et al.
American Journal of Orthodontics and Dentofacial Orthopedics : Official Publication of the American Association of Orthodontists, Its Constituent Societies, and the American Board of Orthodontics|March 5, 2013
Evaluation of the severity of malocclusions in children affected by osteogenesis imperfecta with the peer assessment rating and discrepancy indexesJean Rizkallah, Stephane Schwartz, Frank Rauch, et al.
American Journal of Human Genetics|February 17, 2015
Cole-Carpenter syndrome is caused by a heterozygous missense mutation in P4HBFrank Rauch, Somayyeh Fahiminiya, Jacek Majewski, et al.
American Journal of Human Genetics|June 2, 2015
Homozygosity for frameshift mutations in XYLT2 result in a spondylo-ocular syndrome with bone fragility, cataracts, and hearing defectsCraig F Munns, Somayyeh Fahiminiya, Nabin Poudel, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Pediatric Endocrinology Reviews : PER|July 18, 2013
Emerging concepts in pediatric bone diseaseFrancis Glorieux
Bulletin De L'Academie Nationale De Medecine|July 31, 2002
[Vitamin D and pregnancy]Bernard-Louis Salle, Edgar Delvin, Francis Glorieux
Pediatrics|February 4, 2003
Safety profile of frequent short courses of oral glucocorticoids in acute pediatric asthma: impact on bone metabolism, bone density, and adrenal functionFrancine M Ducharme, Gilles Chabot, Constantin Polychronakos, et al.
JBMR Plus|July 27, 2019
Cone-Beam Computed Tomography of Osteogenesis Imperfecta Types III and IV: Three-Dimensional Evaluation of Craniofacial Features and Upper AirwaysNatalie Reznikov, Didem Dagdeviren, Faleh Tamimi, et al.
Journal of Pediatric Rehabilitation Medicine|July 16, 2011
Activities and participation in young adults with osteogenesis imperfectaKathleen Montpetit, Noémi Dahan-Oliel, Joanne Ruck-Gibis, et al.
Bone|July 31, 2020
Assessment of longitudinal bone growth in osteogenesis imperfecta using metacarpophalangeal pattern profilesDamian Rauch, Marie-Eve Robinson, Cristian Seiltgens, et al.
Bone|August 15, 2022
Craniofacial and dental phenotype of two girls with osteogenesis imperfecta due to mutations in CRTAPJuliana Marulanda, Karissa Ludwig, Francis Glorieux, et al.
American Journal of Orthodontics and Dentofacial Orthopedics : Official Publication of the American Association of Orthodontists, Its Constituent Societies, and the American Board of Orthodontics|March 5, 2013
Evaluation of the severity of malocclusions in children affected by osteogenesis imperfecta with the peer assessment rating and discrepancy indexesJean Rizkallah, Stephane Schwartz, Frank Rauch, et al.
American Journal of Human Genetics|February 17, 2015
Cole-Carpenter syndrome is caused by a heterozygous missense mutation in P4HBFrank Rauch, Somayyeh Fahiminiya, Jacek Majewski, et al.
American Journal of Human Genetics|June 2, 2015
Homozygosity for frameshift mutations in XYLT2 result in a spondylo-ocular syndrome with bone fragility, cataracts, and hearing defectsCraig F Munns, Somayyeh Fahiminiya, Nabin Poudel, et al.
Pageof 2