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Bone histomorphometry: Standardization of nomenclature, symbols, and units: Report of the asbmr histomorphometry nomenclature committee
A committee of the Society to develop a unified system of termnology, suitable for adoption by the Journal of Bone and Mineral Research as part of its Instructions to Authors is formed, and is as complex and conceptually difficult as the field with which it deals.
Standardized nomenclature, symbols, and units for bone histomorphometry: A 2012 update of the report of the ASBMR Histomorphometry Nomenclature Committee
- D. Dempster, J. Compston, A. Parfitt
- MedicineJournal of bone and mineral research : the…
- 1 January 2013
The key revisions include omission of terminology used before 1987, recommendations regarding the parameters and technical information that should be included in all histomorphometry articles, recommendations on how to handle dynamic parameters of bone formation in settings of low bone turnover, and updating of references.
LDL Receptor-Related Protein 5 (LRP5) Affects Bone Accrual and Eye Development
Cyclic administration of pamidronate in children with severe osteogenesis imperfecta.
- F. Glorieux, N. Bishop, H. Plotkin, G. Chabot, G. Lanoue, R. Travers
- MedicineThe New England journal of medicine
- 1 October 1998
In children with severe osteogenesis imperfecta, cyclic administration of intravenous pamidronate improved clinical outcomes, reduced bone resorption, and increased bone density.
Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen: regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycans
The data on genotype–phenotype relationships indicate that the two collagen chains play very different roles in matrix integrity and that phenotype depends on intracellular and extracellular events.
Lrp5 Controls Bone Formation by Inhibiting Serotonin Synthesis in the Duodenum
DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis
Hypophosphatemia is a genetically heterogeneous disease. Here, we mapped an autosomal recessive form (designated ARHP) to chromosome 4q21 and identified homozygous mutations in DMP1 (dentin matrix…
CRTAP Is Required for Prolyl 3- Hydroxylation and Mutations Cause Recessive Osteogenesis Imperfecta
Type V Osteogenesis Imperfecta: A New Form of Brittle Bone Disease
- F. Glorieux, F. Rauch, N. Bishop
- Medicine, BiologyJournal of bone and mineral research : the…
- 1 September 2000
OI type V is a new form of autosomal dominant OI, which does not appear to be associated with collagen type I mutations, and the genetic defect underlying this disease remains to be elucidated.