Results 51 to 60 of about 4,451 (219)

Isolated olecranon fractures in children affected by osteogenesis imperfecta type I treated with single screw or tension band wiring system: outcomes and pitfalls in relation to bone mineral density [PDF]

, 2017
The purpose of this study is to compare the results of 2 techniques, tension band wiring (TBW) and fixation with screws, in olecranon fractures in children affected with osteogenesis imperfecta (OI) type I.
D'Eufemia, Patrizia, De Cristo, Claudia, Graci, Jole, Martini, Lorena, Persiani, Pietro, Ranaldi, Filippo M., Villani, Ciro, Zambrano, Anna   +7 more
core   +1 more source

Genetic aspects of dental disorders [PDF]

, 1998
The document attached has been archived with permission from the Australian Dental Association. An external link to the publisher’s copy is included.This paper reviews past and present applications of quantitative and molecular genetics to dental ...
Aldred MJ, Arte S., Barnett ML., Bartold PM., Baum BJ, Beaty TH, Blackwell CC, Boraas JC, Boughman JA, Boughman JA, Boughman JA, Brown T., Byers PH, Cawson RA., Cheverud JM, Chung C., Chung CS, Chung CS, Chung CS, Conneally PM, Crall MG, Crosby AH, Crowley CA, Delgado WA, Dempsey PJ, Deutsch D., DeVries RR, Elston RC., Finn SB., Fisher RA., Gedda L., George A., Goodman HO, Gorlin RJ, Hart TC., Hassell TM, Hattab FN, Houwink B., Hunt HR, Hunt HR, Hunter WS., Kaslick RS, Katz J., King L., Kirstilia V., Lagerstrom M., Laine T., Lauweryns I., Lauweryns I., Leknes KN, Lundstrom A., MacDougall M., Marazita ML, Marazita ML, Markovic MD., Michalewicz BS., Michalowicz BS, Moller E., Moss ML., Peltomaki T., Potter RH., Potter RH., Proffit WR., Reinholdt J., Roulsten D., Shapira L., Slavkin HC., Smith RJ, Takashiba S., Townsend GC, Townsend GC, Townsend GC, Townsend GC, Towsend G., Varrela J., White R., Whitney C., Willett NP, Wynne SE, Zambon JJ, Zambon JJ   +80 more
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Stomatološko liječenje kod osteogenesis imperfecta [PDF]

, 2017
Osteogenesis imperfecta is a very rare heterogeneous genetic disorder associated with the development of connective tissue resulting in fragile bones and frequent fractures.
Hrvoje Brkić, Ivana Savić Pavičin
core   +2 more sources

Variability of systemic and oro-dental phenotype in two families with non-lethal Raine syndrome with FAM20C mutations [PDF]

, 2015
Background: Raine syndrome (RS) is a rare autosomal recessive bone dysplasia typified by osteosclerosis and dysmorphic facies due to FAM20C mutations. Initially reported as lethal in infancy, survival is possible into adulthood. We describe the molecular
A Linde, A Rejjal, AE Kan, Alan J Mighell, Ana Carolina Acevedo, AX Acosta, C Chaussain-Miller, C Gaucher, Caroline Lourenço de Lima, Chris F Inglehearn, Claire E L Smith, Clare V Logan, CM Giachelli, Colin A Johnson, D Chitayat, D Nalbant, David A Parry, E Katchburian, FK Ababneh, G Hulskamp, G Jaureguiberry, GS Kochar, HM Kingston, HO Ishikawa, J Dong, J Hao, J Raine, James A Poulter, K Al-Mane, KA Al Mane, L Ye, LI Al-Gazali, Lilian M Paula, Luiz Claudio Castro, LW Fisher, M Dure-Molla de la, M Fradin, M Koob, MA DePristo, MA Simpson, MA Simpson, P Vogel, Paulo Marcio Yamaguti, PJ Patel, Priscila Gomes Alves, PS Hart, S Takeyari, SA Shalev, SH Rafaelsen, SK Wang, SK Wang, SM Hebsgaard, T Gunes, T Mahafza, T Sreenath, V Faundes, VS Tagliabracci, X Wang, X Wang, X Wang, X Wang, Y Kinoshita   +61 more
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Sequentially Functional And Asthetic Restoration Of Severe Dentin Dysplasia

International Dental Journal
Introduction: This case report introduced sequentially functional and aesthetic restoration on a patient with dentin dysplasia type II (DD-II) accompanied by severe tooth wear. Case description: An eight-year-old girl with severe tooth wear presented for
Xuemei Liu, Xu Chen
doaj   +1 more source

A Case of Dentinogenesis Imperfecta Treated with Submerged Root Technique [PDF]

Journal of Clinical and Diagnostic Research, 2015
Dentinogenesis imperfecta (DGI), an autosomal dominant trait, is one of the most common hereditary disorders affecting both the formation and mineralization of dentin. Either or both primary and permanent dentition is affected by it.
Ginjupally Uday, Bhanu Chandar, J. Srilakshmi, Tanya Khaitan, B. Balaji Babu   +4 more
doaj   +1 more source

Recessive osteogenesis imperfecta caused by LEPRE1 mutations: clinical documentation and identification of the splice form responsible for prolyl 3-hydroxylation [PDF]

, 2009
: Background: Recessive forms of osteogenesis imperfecta (OI) may be caused by mutations in LEPRE1, encoding prolyl 3-hydroxylase-1 (P3H1) or in CRTAP, encoding cartilage associated protein.
Coucke, Paul, De Paepe, Anne, Gevaert, Kris, Kayserili, H., Leroy, J. G., Malfait, Fransiska, Megarbane, A., Mortier, Geert, Symoens, Sofie, Willaert, Andy   +9 more
core   +2 more sources

Serum creatine kinase isoenzymes in children with osteogenesis imperfecta [PDF]

, 2017
This study evaluates serum creatine kinase isoenzyme activity in children with osteogenesis imperfecta to determine its usefulness as a biochemical marker during treatment with bisphosphonate.
Celli, L, Celli, M., D'Eufemia, Patrizia, Finocchiaro, R, Finocchiaro, S, Lodato, V, Persiani, Pietro, Turchetti, A, Zambrano, A   +8 more
core   +1 more source

Hypoplastic amelogenesis imperfecta with multiple impacted teeth: report of two cases [PDF]

, 2010
Amelogenesis Imperfecta (AI) represents a group of developmental conditions, genomic in origin, which affect the structure and clinical appearance of enamel of all or nearly all the teeth in a more or less equal manner.
Aarthi Nisha, Aarthi, Harish, B.N., Reddy, Sujatha S.   +2 more
core   +1 more source

Conditional Knockout of Raptor/mTORC1 Results in Dentin Malformation

Frontiers in Physiology, 2019
mTORC1 signaling plays an important role in extracellular and intracellular signals, including growth factors, nutrients, energy metabolism, and stress. However, the functional role of mTORC1 in dentinogenesis is unknown.
Furong Xie, Furong Xie, Furong Xie, Qinggang Dai, Qinggang Dai, Qinggang Dai, Xiao Liu, Xiao Liu, Xiao Liu, Jun Wang, Jun Wang, Jun Wang   +11 more
doaj   +1 more source