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Quoted phrase not found in phrase index: "Osteogenesis imperfecta type 8"
Page 1
Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia.
Barron MJ, McDonnell ST, Mackie I, Dixon MJ. Barron MJ, et al. Orphanet J Rare Dis. 2008 Nov 20;3:31. doi: 10.1186/1750-1172-3-31. Orphanet J Rare Dis. 2008. PMID: 19021896 Free PMC article. Review.
DGI is reported to have an incidence of 1 in 6,000 to 1 in 8,000, whereas that of DD type 1 is 1 in 100,000. Clinically, the teeth are discoloured and show structural defects such as bulbous crowns and small pulp chambers radiographically. ...Currently, three sub-ty …
DGI is reported to have an incidence of 1 in 6,000 to 1 in 8,000, whereas that of DD type 1 is 1 in 100,000. Clinically, the t …
Missing and unerupted teeth in osteogenesis imperfecta.
Taqi D, Moussa H, Schwinghamer T, Vieira AR, Dagdeviren D, Retrouvey JM, Rauch F, Tamimi F; Members of the BBDC. Taqi D, et al. Bone. 2021 Sep;150:116011. doi: 10.1016/j.bone.2021.116011. Epub 2021 May 18. Bone. 2021. PMID: 34020077
INTRODUCTION: Osteogenesis imperfecta (OI) is a genetic disorder characterized by bone fragility and craniofacial and dental abnormalities such as congenitally missing teeth and teeth that failed to erupt which are believed to be doubled in OI patients than normal p …
INTRODUCTION: Osteogenesis imperfecta (OI) is a genetic disorder characterized by bone fragility and craniofacial and dental a …
Collagen transport and related pathways in Osteogenesis Imperfecta.
Claeys L, Storoni S, Eekhoff M, Elting M, Wisse L, Pals G, Bravenboer N, Maugeri A, Micha D. Claeys L, et al. Hum Genet. 2021 Aug;140(8):1121-1141. doi: 10.1007/s00439-021-02302-2. Epub 2021 Jun 24. Hum Genet. 2021. PMID: 34169326 Free PMC article. Review.
Osteogenesis Imperfecta (OI) comprises a heterogeneous group of patients who share bone fragility and deformities as the main characteristics, albeit with different degrees of severity. Phenotypic variation also exists in other connective tissue aspects of the disea …
Osteogenesis Imperfecta (OI) comprises a heterogeneous group of patients who share bone fragility and deformities as the main …
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 …
Scoliosis in osteogenesis imperfecta: identifying the genetic and non-genetic factors affecting severity and progression from longitudinal data of 290 patients.
Chen P, Zhou Y, Tan Z, Lin Y, Lin DL, Wu J, Li Z, Shek HT, Wu J, Hu Y, Zhu F, Chan D, Cheung KM, To MK. Chen P, et al. Orphanet J Rare Dis. 2023 Sep 20;18(1):295. doi: 10.1186/s13023-023-02906-z. Orphanet J Rare Dis. 2023. PMID: 37730650 Free PMC article.
BACKGROUND: Scoliosis is widely prevalent among osteogenesis imperfecta (OI) patients, and is progressive with age. However, factors affecting scoliosis in OI are not well known. ...CONCLUSION: The severity and progression of scoliosis in osteogenesis impe …
BACKGROUND: Scoliosis is widely prevalent among osteogenesis imperfecta (OI) patients, and is progressive with age. However, f …
Keratoconus tomographic indices in osteogenesis imperfecta.
Correia Barão R, Santos M, Marques RE, Quintas AM, Guerra P. Correia Barão R, et al. Graefes Arch Clin Exp Ophthalmol. 2023 Sep;261(9):2585-2592. doi: 10.1007/s00417-023-06059-4. Epub 2023 Apr 19. Graefes Arch Clin Exp Ophthalmol. 2023. PMID: 37074408 Free PMC article.
PURPOSE: Osteogenesis imperfecta (OI) is a rare inherited disease affecting collagen-rich tissues. ...Patients and controls underwent comprehensive ophthalmological examination including corneal Scheimpflug tomography with a Pentacam HR device (Oculus Optikgerate Gm …
PURPOSE: Osteogenesis imperfecta (OI) is a rare inherited disease affecting collagen-rich tissues. ...Patients and controls un …
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 …
Long-term follow-up in osteogenesis imperfecta type VI.
Trejo P, Palomo T, Montpetit K, Fassier F, Sato A, Glorieux FH, Rauch F. Trejo P, et al. Osteoporos Int. 2017 Oct;28(10):2975-2983. doi: 10.1007/s00198-017-4141-x. Epub 2017 Jul 9. Osteoporos Int. 2017. PMID: 28689307
This retrospective study on long-term outcomes in osteogenesis imperfecta type VI found that patients who received intravenous bisphosphonate treatment had an increase in lumbar spine areal bone mineral density, a higher final height z-score, and some reshapi …
This retrospective study on long-term outcomes in osteogenesis imperfecta type VI found that patients who received intr …
Severe osteogenesis imperfecta Type-III and its challenging treatment in newborn and preschool children. A systematic review.
Sinikumpu JJ, Ojaniemi M, Lehenkari P, Serlo W. Sinikumpu JJ, et al. Injury. 2015 Aug;46(8):1440-6. doi: 10.1016/j.injury.2015.04.021. Epub 2015 Apr 22. Injury. 2015. PMID: 25943292 Review.
Osteogenesis imperfecta (OI) is a group of genetic disorders, of which Type III is the most severe among survivors. ...In this systematic review we describe the present state-of-art in treating the most severe type of OI in newborn and preschool childr …
Osteogenesis imperfecta (OI) is a group of genetic disorders, of which Type III is the most severe among survivors. ... …
Premenopausal osteoporosis: how to treat?
Martínez-Morillo M, Grados D, Holgado S. Martínez-Morillo M, et al. Reumatol Clin. 2012 Mar-Apr;8(2):93-7. doi: 10.1016/j.reuma.2011.05.011. Epub 2011 Aug 6. Reumatol Clin. 2012. PMID: 22089064 Free article. Review.
This article will review the measures to apply depending on the type of premenopausal osteoporosis, based on current scientific evidence....
This article will review the measures to apply depending on the type of premenopausal osteoporosis, based on current scientific evide …
159 results