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2007 5
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84 results

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Page 1
Paget's disease of bone.
Appelman-Dijkstra NM, Papapoulos SE. Appelman-Dijkstra NM, et al. Best Pract Res Clin Endocrinol Metab. 2018 Oct;32(5):657-668. doi: 10.1016/j.beem.2018.05.005. Epub 2018 May 26. Best Pract Res Clin Endocrinol Metab. 2018. PMID: 30449547 Review.
Paget's disease of bone is a focal disorder of bone remodelling that progresses slowly and leads to changes in the shape and size of affected bones and to skeletal, articular and vascular complications. ...
Paget's disease of bone is a focal disorder of bone remodelling that progresses slowly and leads to changes in the shap …
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.
In this review, we examine 25 selected hereditary metabolic bone diseases and recognized genetic variations of 78 genes that represent each of the three groups, including sclerosing bone disorders, disorders of defective bone mineralization and disorder of bone …
In this review, we examine 25 selected hereditary metabolic bone diseases and recognized genetic variations of 78 genes that represent each …
Aplastic anemia: Etiology, molecular pathogenesis, and emerging concepts.
Shallis RM, Ahmad R, Zeidan AM. Shallis RM, et al. Eur J Haematol. 2018 Dec;101(6):711-720. doi: 10.1111/ejh.13153. Epub 2018 Oct 10. Eur J Haematol. 2018. PMID: 30055055 Review.
Aplastic anemia (AA) is rare disorder of bone marrow failure which if severe and not appropriately treated is highly fatal. ...
Aplastic anemia (AA) is rare disorder of bone marrow failure which if severe and not appropriately treated is highly fa …
Imaging of Paget's disease of bone.
Winn N, Lalam R, Cassar-Pullicino V. Winn N, et al. Wien Med Wochenschr. 2017 Feb;167(1-2):9-17. doi: 10.1007/s10354-016-0517-3. Epub 2016 Oct 19. Wien Med Wochenschr. 2017. PMID: 27761746 Review. English.
Paget's disease of bone is a disorder of bone remodelling, leading to changes in the architecture and overall appearance of the bone. ...
Paget's disease of bone is a disorder of bone remodelling, leading to changes in the architecture and overall appearanc …
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 …
Paget's disease of bone.
Griz L, Caldas G, Bandeira C, Assunção V, Bandeira F. Griz L, et al. Arq Bras Endocrinol Metabol. 2006 Aug;50(4):814-22. doi: 10.1590/s0004-27302006000400026. Arq Bras Endocrinol Metabol. 2006. PMID: 17117306 Review.
Paget's disease of bone is a focal disorder of bone remodeling accompanied initially by an increase in bone resorption, followed by a disorganized and excessive formation of bone, leading to pain, fractures and deformities. ...
Paget's disease of bone is a focal disorder of bone remodeling accompanied initially by an increase in bone resorption, …
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 opinio …
Hypophosphatasia (HPP) is a rare inherited disorder of bone and mineral metabolism caused by loss of function mutations …
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. ...
Hypophosphatasia (HPP) is a rare inherited disorder of bone affecting approximately 500 to 600 known individuals in the …
Treating osteomyelitis: antibiotics and surgery.
Rao N, Ziran BH, Lipsky BA. Rao N, et al. Plast Reconstr Surg. 2011 Jan;127 Suppl 1:177S-187S. doi: 10.1097/PRS.0b013e3182001f0f. Plast Reconstr Surg. 2011. PMID: 21200289 Review.
BACKGROUND: Osteomyelitis is an inflammatory disorder of bone caused by infection leading to necrosis and destruction. ...
BACKGROUND: Osteomyelitis is an inflammatory disorder of bone caused by infection leading to necrosis and destruction. …
Renal bone disease.
Sprague SM. Sprague SM. Curr Opin Endocrinol Diabetes Obes. 2010 Dec;17(6):535-9. doi: 10.1097/MED.0b013e3283400945. Curr Opin Endocrinol Diabetes Obes. 2010. PMID: 21030840 Review.
PURPOSE OF REVIEW: Renal osteodystrophy is a complex disorder of bone associated with chronic kidney disease (CKD). Disturbances in mineral metabolism, which include, phosphate retention, hypocalcemia, vitamin D deficiency, and hyperparathyroidism develop ear …
PURPOSE OF REVIEW: Renal osteodystrophy is a complex disorder of bone associated with chronic kidney disease (CKD). Dis …
84 results