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Bonekey Reports
|
August 17, 2013
Serotonin: good or bad for bone
Marie-Christine de Vernejoul, Corinne Collet, Yasmine Chabbi-Achengli
European Journal of Medical Genetics
|
March 6, 2014
Novel SOST gene mutation in a sclerosteosis patient from Morocco: a case report
Mohamed Reda Belkhribchia, Corinne Collet, Jean-Louis Laplanche, et al.
Joint Bone Spine
|
July 3, 2016
First case of osteopathia striata with cranial sclerosis in an adult male with Klinefelter syndrome
Melanie Fradin, Corinne Collet, Isabelle Ract, et al.
Case Reports in Genetics
|
February 24, 2016
Osteoporosis-Pseudoglioma in a Mauritanian Child due to a Novel Mutation in LRP5
Noura Biha, S M Ghaber, M M Hacen, et al.
Joint Bone Spine
|
April 1, 2006
Genetics of Paget's disease of bone
Laëtitia Michou, Corinne Collet, Jean-Louis Laplanche, et al.
Clinical Genetics
|
February 22, 2024
Novel variant in LRP6 associated with unusual and severe clinical presentation: Case report
Anaïk Previdi, Christèle Dubourg, Valérie Cormier Daire, et al.
Bone
|
November 2, 2023
Long-term follow-up of severe autosomal recessive SP7-related bone disorder
Lucas W Gauthier, Elisabeth Fontanges, Roland Chapurlat, et al.
The American Journal of Pathology
|
April 26, 2007
Overexpression of the transcriptional factor Runx2 in osteoblasts abolishes the anabolic effect of parathyroid hormone in vivo
Didier Merciris, Caroline Marty, Corinne Collet, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 8, 2024
Genetics and bone mineral density predict the fractures in adults with osteogenesis imperfecta: a prospective study
Camille Blandin, Corinne Collet, Agnes Ostertag, et al.
Bone
|
January 4, 2020
Genetic testing is useful in adults with limited phenotypes of genetic skeletal conditions
Marie Cottard, Emmanuelle Vignot, Elisabeth Fontanges, et al.
Page
of 10
Search research articles
Search
Showing results (1-10 of 93) with videos related to
Sort By:
Page
of 10
Bonekey Reports
|
August 17, 2013
Serotonin: good or bad for bone
Marie-Christine de Vernejoul, Corinne Collet, Yasmine Chabbi-Achengli
European Journal of Medical Genetics
|
March 6, 2014
Novel SOST gene mutation in a sclerosteosis patient from Morocco: a case report
Mohamed Reda Belkhribchia, Corinne Collet, Jean-Louis Laplanche, et al.
Joint Bone Spine
|
July 3, 2016
First case of osteopathia striata with cranial sclerosis in an adult male with Klinefelter syndrome
Melanie Fradin, Corinne Collet, Isabelle Ract, et al.
Case Reports in Genetics
|
February 24, 2016
Osteoporosis-Pseudoglioma in a Mauritanian Child due to a Novel Mutation in LRP5
Noura Biha, S M Ghaber, M M Hacen, et al.
Joint Bone Spine
|
April 1, 2006
Genetics of Paget's disease of bone
Laëtitia Michou, Corinne Collet, Jean-Louis Laplanche, et al.
Clinical Genetics
|
February 22, 2024
Novel variant in LRP6 associated with unusual and severe clinical presentation: Case report
Anaïk Previdi, Christèle Dubourg, Valérie Cormier Daire, et al.
Bone
|
November 2, 2023
Long-term follow-up of severe autosomal recessive SP7-related bone disorder
Lucas W Gauthier, Elisabeth Fontanges, Roland Chapurlat, et al.
The American Journal of Pathology
|
April 26, 2007
Overexpression of the transcriptional factor Runx2 in osteoblasts abolishes the anabolic effect of parathyroid hormone in vivo
Didier Merciris, Caroline Marty, Corinne Collet, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 8, 2024
Genetics and bone mineral density predict the fractures in adults with osteogenesis imperfecta: a prospective study
Camille Blandin, Corinne Collet, Agnes Ostertag, et al.
Bone
|
January 4, 2020
Genetic testing is useful in adults with limited phenotypes of genetic skeletal conditions
Marie Cottard, Emmanuelle Vignot, Elisabeth Fontanges, et al.
Page
of 10