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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1976 1
1989 1
1997 1
2006 1
2007 1
2008 1
2010 1
2013 1
2015 1
2016 3
2017 1
2019 1
2022 1
2023 1
2024 1

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Page 1
Hereditary Metabolic Bone Diseases: A Review of Pathogenesis, Diagnosis and Management.
Charoenngam N, Nasr A, Shirvani A, Holick MF. Charoenngam N, et al. Genes (Basel). 2022 Oct 17;13(10):1880. doi: 10.3390/genes13101880. Genes (Basel). 2022. PMID: 36292765 Free PMC article. Review.
Hereditary metabolic bone diseases are characterized by genetic abnormalities in skeletal homeostasis and encompass one of the most diverse groups among rare diseases. In this review, we examine 25 selected hereditary metabolic bone diseases and recognized genetic v …
Hereditary metabolic bone diseases are characterized by genetic abnormalities in skeletal homeostasis and encompass one of the most d …
Hypophosphatasia in Adults: Clinical Assessment and Treatment Considerations.
Shapiro JR, Lewiecki EM. Shapiro JR, et al. J Bone Miner Res. 2017 Oct;32(10):1977-1980. doi: 10.1002/jbmr.3226. Epub 2017 Aug 16. J Bone Miner Res. 2017. PMID: 28731215 Free article. Review.
Hypophosphatasia (HPP) is a rare inherited disorder of bone affecting approximately 500 to 600 known individuals in the United States. ...This discussion addresses diagnostic and treatment considerations for adults with HPP. 2017 American Society for Bone and …
Hypophosphatasia (HPP) is a rare inherited disorder of bone affecting approximately 500 to 600 known individuals in the United …
Hypophosphatasia: Canadian update on diagnosis and management.
Khan AA, Josse R, Kannu P, Villeneuve J, Paul T, Van Uum S, Greenberg CR. Khan AA, et al. Osteoporos Int. 2019 Sep;30(9):1713-1722. doi: 10.1007/s00198-019-04921-y. Epub 2019 Mar 26. Osteoporos Int. 2019. PMID: 30915507 Review.
Hypophosphatasia (HPP) is a rare inherited disorder of bone and mineral metabolism caused by loss of function mutations in the ALPL gene. ...The following consensus recommendations were developed based on the highest level of evidence as well as expert opinion. RESU …
Hypophosphatasia (HPP) is a rare inherited disorder of bone and mineral metabolism caused by loss of function mutations in the …
Diagnosis and treatment of Paget's disease of bone: a mini-review.
Ferraz-de-Souza B, Correa PH. Ferraz-de-Souza B, et al. Arq Bras Endocrinol Metabol. 2013 Nov;57(8):577-82. doi: 10.1590/s0004-27302013000800001. Arq Bras Endocrinol Metabol. 2013. PMID: 24343625 Review.
Paget's disease of bone (PDB) is a chronic progressive disorder of bone metabolism that may go undetected for many years, and endocrinologists should be alert to its clinical signs and promptly diagnose and treat PDB before it results in irreversible complica …
Paget's disease of bone (PDB) is a chronic progressive disorder of bone metabolism that may go undetected for many year …
The rationale for intermittent administration of PTH in the management of mineral and bone disorder of chronic kidney disease.
Pazianas M, Miller PD. Pazianas M, et al. J Nephrol. 2024 Mar;37(2):337-342. doi: 10.1007/s40620-023-01642-8. Epub 2023 May 12. J Nephrol. 2024. PMID: 37171706 Review.
A major complication of chronic kidney disease is the derangement of mineral metabolism, leading to increased risk of fractures and cardiovascular mortality. Current therapeutic regimens are focused on reducing parathyroid hormone levels caused by secondary hyperparathyroi …
A major complication of chronic kidney disease is the derangement of mineral metabolism, leading to increased risk of fractures and cardiova …
Best practices in the evaluation and treatment of foramen magnum stenosis in achondroplasia during infancy.
White KK, Bompadre V, Goldberg MJ, Bober MB, Campbell JW, Cho TJ, Hoover-Fong J, Mackenzie W, Parnell SE, Raggio C, Rapoport DM, Spencer SA, Savarirayan R. White KK, et al. Am J Med Genet A. 2016 Jan;170A(1):42-51. doi: 10.1002/ajmg.a.37394. Epub 2015 Sep 23. Am J Med Genet A. 2016. PMID: 26394886
Achondroplasia is the most common inherited disorder of bone growth (skeletal dysplasia). Despite this fact, consistent and evidence-based management approaches to recognized, life-threatening complications, such as foramen magnum stenosis, are lacking. ...It is hop …
Achondroplasia is the most common inherited disorder of bone growth (skeletal dysplasia). Despite this fact, consistent and ev …
Pharmacologic management of Paget's disease.
Stumpf JL. Stumpf JL. Clin Pharm. 1989 Jul;8(7):485-95. Clin Pharm. 1989. PMID: 2666012 Review.
Paget's disease is a bone disorder of unknown etiology primarily affecting the elderly. Overactive bone resorption leads to the accelerated formation of disorganized, weak bone. ...
Paget's disease is a bone disorder of unknown etiology primarily affecting the elderly. Overactive bone resorption lead …
KDIGO clinical practice guidelines for the diagnosis, evaluation, prevention, and treatment of mineral and bone disorders in chronic kidney disease.
Matuszkiewicz-Rowińska J. Matuszkiewicz-Rowińska J. Pol Arch Med Wewn. 2010 Jul;120(7-8):300-6. Pol Arch Med Wewn. 2010. PMID: 20693962 Free article. Review.
After almost 4 years of intensive work, the mineral and bone disorder of chronic kidney disease guidelines were presented during the American Society of Nephrology Renal Week at the end of 2008, to be finally published in Kidney International, August 2009. ...Finall …
After almost 4 years of intensive work, the mineral and bone disorder of chronic kidney disease guidelines were presented duri …
Basilar invagination in osteogenesis imperfecta and related osteochondrodysplasias: medical and surgical management.
Sawin PD, Menezes AH. Sawin PD, et al. J Neurosurg. 1997 Jun;86(6):950-60. doi: 10.3171/jns.1997.86.6.0950. J Neurosurg. 1997. PMID: 9171173
Osteogenesis imperfecta (OI) is a heritable disorder of bone development caused by defective collagen synthesis. ...This study represents the largest series to date addressing craniovertebral anomalies in OI and related congenital bone softening disorders....
Osteogenesis imperfecta (OI) is a heritable disorder of bone development caused by defective collagen synthesis. ...This study …
A neglected requirement for optimizing treatment of age-related osteoporosis: Replenishing the skeleton's base reservoir with net base-producing diets.
Sebastian A, Frassetto LA. Sebastian A, et al. Med Hypotheses. 2016 Jun;91:103-108. doi: 10.1016/j.mehy.2016.04.027. Epub 2016 Apr 16. Med Hypotheses. 2016. PMID: 27142156
Osteoporosis is a disorder of bone in which the mass of the bone is reduced and the bone's architecture at the microscopic level is disordered. ...Age related osteoporosis is a common type of osteoporosis that occurs with aging in both men and women us …
Osteoporosis is a disorder of bone in which the mass of the bone is reduced and the bone's architecture at the m …
14 results