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Quoted phrase not found in phrase index: "Osteogenesis imperfecta type 9"
Page 1
Bisphosphonate therapy for osteogenesis imperfecta.
Dwan K, Phillipi CA, Steiner RD, Basel D. Dwan K, et al. Cochrane Database Syst Rev. 2016 Oct 19;10(10):CD005088. doi: 10.1002/14651858.CD005088.pub4. Cochrane Database Syst Rev. 2016. PMID: 27760454 Free PMC article. Review.
BACKGROUND: Osteogenesis imperfecta is caused by a genetic defect resulting in an abnormal type I collagen bone matrix which typically results in multiple fractures with little or no trauma. Bisphosphonates are used in an attempt to increase bone mineral dens …
BACKGROUND: Osteogenesis imperfecta is caused by a genetic defect resulting in an abnormal type I collagen bone matrix …
Mortality and morbidity in patients with osteogenesis imperfecta in Denmark.
Folkestad L. Folkestad L. Dan Med J. 2018 Apr;65(4):B5454. Dan Med J. 2018. PMID: 29619932 Free article. Review.
Ostegenesis imperfecta (OI) is a hereditary disease of the connective tissue caused by mutations to, mainly, the genes that are involved in the biosynthesis of collagen type 1. ...The study included 39 patients with OI type I, and 39 healthy age and gender ma …
Ostegenesis imperfecta (OI) is a hereditary disease of the connective tissue caused by mutations to, mainly, the genes that are invol …
Prevalence and Hospital Admissions in Patients With Osteogenesis Imperfecta in The Netherlands: A Nationwide Registry Study.
Storoni S, Treurniet S, Maugeri A, Pals G, van den Aardweg JG, van der Pas SL, Elting MW, Kloen P, Micha D, Eekhoff EMW. Storoni S, et al. Front Endocrinol (Lausanne). 2022 Apr 25;13:869604. doi: 10.3389/fendo.2022.869604. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 35546999 Free PMC article.
Osteogenesis Imperfecta (OI) is a complex disease caused by genetic alterations in production of collagen type I, and collagen-related proteins. ...The median annual incidence risk of OI between 1992 and 2019 was 6.5 per 100,000 live births. Furthermore, pati …
Osteogenesis Imperfecta (OI) is a complex disease caused by genetic alterations in production of collagen type I, and c …
Genotype and phenotype analysis of Taiwanese patients with osteogenesis imperfecta.
Lin HY, Chuang CK, Su YN, Chen MR, Chiu HC, Niu DM, Lin SP. Lin HY, et al. Orphanet J Rare Dis. 2015 Dec 1;10:152. doi: 10.1186/s13023-015-0370-2. Orphanet J Rare Dis. 2015. PMID: 26627451 Free PMC article.
BACKGROUND: Osteogenesis imperfecta (OI) is a congenital disorder characterized by increased bone fragility and low bone mass. ...RESULTS: Thirty-seven COL1A1 and COL1A2 mutations were identified, including 28 COL1A1 mutations and 9 COL1A2 mutations. Fifteen …
BACKGROUND: Osteogenesis imperfecta (OI) is a congenital disorder characterized by increased bone fragility and low bone mass. …
Deciphering the Relevance of Bone ECM Signaling.
Alcorta-Sevillano N, Macías I, Infante A, Rodríguez CI. Alcorta-Sevillano N, et al. Cells. 2020 Dec 7;9(12):2630. doi: 10.3390/cells9122630. Cells. 2020. PMID: 33297501 Free PMC article. Review.
The main inorganic components of the ECM are calcium-deficient apatite and trace elements, while the organic ECM consists of collagen type I and noncollagenous proteins. Bone ECM dynamically interacts with osteoblasts and osteoclasts to regulate the formation of new bone d …
The main inorganic components of the ECM are calcium-deficient apatite and trace elements, while the organic ECM consists of collagen typ …
Osteogenesis Imperfecta: The Impact of Genotype and Clinical Phenotype on Adiposity and Resting Energy Expenditure.
Ballenger KL, Tugarinov N, Talvacchio SK, Knue MM, Dang Do AN, Ahlman MA, Reynolds JC, Yanovski JA, Marini JC. Ballenger KL, et al. J Clin Endocrinol Metab. 2022 Jan 1;107(1):67-76. doi: 10.1210/clinem/dgab679. J Clin Endocrinol Metab. 2022. PMID: 34519823 Free PMC article.
CONTEXT: Mutations in type I collagen or collagen-related proteins cause osteogenesis imperfecta (OI). ...OBJECTIVE: This study compares adiposity and resting energy expenditure (REE) in OI and healthy controls (HC), for OI genotype- and Type-associate …
CONTEXT: Mutations in type I collagen or collagen-related proteins cause osteogenesis imperfecta (OI). ...OBJECTIVE: Th …
Gait Deviations in Children With Osteogenesis Imperfecta Type I.
Garman CR, Graf A, Krzak J, Caudill A, Smith P, Harris G. Garman CR, et al. J Pediatr Orthop. 2019 Sep;39(8):e641-e646. doi: 10.1097/BPO.0000000000001062. J Pediatr Orthop. 2019. PMID: 31393309
BACKGROUND: Osteogenesis imperfecta (OI) is a congenital connective tissue disorder often characterized by orthopaedic complications that impact normal gait. ...METHODS: Gait analysis was performed on 44 subjects with type I (11.73.08 y old) and 30 typically …
BACKGROUND: Osteogenesis imperfecta (OI) is a congenital connective tissue disorder often characterized by orthopaedic complic …
Dentinogenesis imperfecta type II in Swedish children and adolescents.
Andersson K, Malmgren B, Åström E, Dahllöf G. Andersson K, et al. Orphanet J Rare Dis. 2018 Aug 22;13(1):145. doi: 10.1186/s13023-018-0887-2. Orphanet J Rare Dis. 2018. PMID: 30134932 Free PMC article.
BACKGROUND: Dentinogenesis imperfecta (DGI) is a heritable disorder of dentin. Genetic analyses have found two subgroups in this disorder: DGI type I, a syndromic form associated with osteogenesis imperfecta (OI), and DGI type II, a non-syndromi …
BACKGROUND: Dentinogenesis imperfecta (DGI) is a heritable disorder of dentin. Genetic analyses have found two subgroups in this diso …
Clinical and genetic analysis in 185 Chinese probands of osteogenesis imperfecta.
Xi L, Zhang H, Zhang ZL. Xi L, et al. J Bone Miner Metab. 2021 May;39(3):416-422. doi: 10.1007/s00774-020-01163-5. Epub 2020 Oct 17. J Bone Miner Metab. 2021. PMID: 33070251
INTRODUCTION: Osteogenesis imperfecta (OI) is a well-known heritable disorder of connective tissue characterized by skeletal fragility and low bone mass. ...Patients with OI types III and IV, especially type III, had a higher proportion of dentinogenesis i …
INTRODUCTION: Osteogenesis imperfecta (OI) is a well-known heritable disorder of connective tissue characterized by skeletal f …
Fracture Patterns Differ Between Osteogenesis Imperfecta and Routine Pediatric Fractures.
Peddada KV, Sullivan BT, Margalit A, Sponseller PD. Peddada KV, et al. J Pediatr Orthop. 2018 Apr;38(4):e207-e212. doi: 10.1097/BPO.0000000000001137. J Pediatr Orthop. 2018. PMID: 29356793
BACKGROUND: It is important to estimate the likelihood that a pediatric fracture is caused by osteogenesis imperfecta (OI), especially the least severe type of OI (type 1). ...We included patients with closed fractures not resulting from motor vehicle …
BACKGROUND: It is important to estimate the likelihood that a pediatric fracture is caused by osteogenesis imperfecta (OI), es …
147 results