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Items: 1 to 20 of 144

1.

WHOLE-BODY VIBRATION EXERCISE IMPROVES FUNCTIONAL PARAMETERS IN PATIENTS WITH OSTEOGENESIS IMPERFECTA: A SYSTEMATIC REVIEW WITH A SUITABLE APPROACH.

Sá-Caputo DC, Dionello CDF, Frederico ÉHFF, Paineiras-Domingos LL, Sousa-Gonçalves CR, Morel DS, Moreira-Marconi E, Unger M, Bernardo-Filho M.

Afr J Tradit Complement Altern Med. 2017 Mar 1;14(3):199-208. doi: 10.21010/ajtcam.v14i3.22. eCollection 2017.

2.

Managing the patient with osteogenesis imperfecta: a multidisciplinary approach.

Marr C, Seasman A, Bishop N.

J Multidiscip Healthc. 2017 Apr 4;10:145-155. doi: 10.2147/JMDH.S113483. eCollection 2017. Review.

3.

Fkbp10 Deletion in Osteoblasts Leads to Qualitative Defects in Bone.

Lietman CD, Lim J, Grafe I, Chen Y, Ding H, Bi X, Ambrose CG, Fratzl-Zelman N, Roschger P, Klaushofer K, Wagermaier W, Schmidt I, Fratzl P, Rai J, Weis M, Eyre D, Keene DR, Krakow D, Lee BH.

J Bone Miner Res. 2017 Jun;32(6):1354-1367. doi: 10.1002/jbmr.3108. Epub 2017 Mar 20.

PMID:
28206698
4.

Nanotechnology in the regulation of stem cell behavior.

Wu KC, Tseng CL, Wu CC, Kao FC, Tu YK, C So E, Wang YK.

Sci Technol Adv Mater. 2013 Oct 11;14(5):054401. eCollection 2013 Oct. Review.

5.

β-Aminopropionitrile-Induced Reduction in Enzymatic Crosslinking Causes In Vitro Changes in Collagen Morphology and Molecular Composition.

Canelón SP, Wallace JM.

PLoS One. 2016 Nov 9;11(11):e0166392. doi: 10.1371/journal.pone.0166392. eCollection 2016.

6.

Childhood Osteoporosis and Presentation of Two Cases with Osteogenesis Imperfecta Type V.

Bratanic N, Dzodan B, Trebusak Podkrajsek K, Bertok S, Ostanek B, Marc J, Battelino T, Avbelj Stefanija M.

Zdr Varst. 2015 Mar 13;54(2):119-25. doi: 10.1515/sjph-2015-0018. eCollection 2015 Jun.

7.

Mutation analysis of the COL1A1 and COL1A2 genes in Vietnamese patients with osteogenesis imperfecta.

Ho Duy B, Zhytnik L, Maasalu K, Kändla I, Prans E, Reimann E, Märtson A, Kõks S.

Hum Genomics. 2016 Aug 12;10(1):27. doi: 10.1186/s40246-016-0083-1.

8.

Osteogenesis imperfecta and clubfoot-a rare combination: Case report and review of the literature.

Persiani P, Ranaldi FM, Martini L, Zambrano A, Celli M, D'Eufemia P, Villani C.

Medicine (Baltimore). 2016 Aug;95(31):e4505. doi: 10.1097/MD.0000000000004505. Review.

9.

Next-generation sequencing of common osteogenesis imperfecta-related genes in clinical practice.

Árvai K, Horváth P, Balla B, Tobiás B, Kató K, Kirschner G, Klujber V, Lakatos P, Kósa JP.

Sci Rep. 2016 Jun 23;6:28417. doi: 10.1038/srep28417.

10.

Osteogenesis Imperfecta Diagnosed from Mandibular and Lower Limb Fractures: A Case Report.

Kobayashi Y, Satoh K, Mizutani H.

Craniomaxillofac Trauma Reconstr. 2016 Jun;9(2):141-4. doi: 10.1055/s-0035-1550063. Epub 2015 Apr 28.

11.

Comparative analysis of gene expression profiles in normal hip human cartilage and cartilage from patients with necrosis of the femoral head.

Liu R, Liu Q, Wang K, Dang X, Zhang F.

Arthritis Res Ther. 2016 May 4;18(1):98. doi: 10.1186/s13075-016-0991-4.

12.
13.

Dental panoramic indices and fractal dimension measurements in osteogenesis imperfecta children under pamidronate treatment.

Apolinário AC, Sindeaux R, de Souza Figueiredo PT, Guimarães AT, Acevedo AC, Castro LC, de Paula AP, de Paula LM, de Melo NS, Leite AF.

Dentomaxillofac Radiol. 2016;45(4):20150400. doi: 10.1259/dmfr.20150400. Epub 2016 Mar 24.

14.

Safety and efficacy of denosumab in children with osteogenesis imperfect--a first prospective trial.

Hoyer-Kuhn H, Franklin J, Allo G, Kron M, Netzer C, Eysel P, Hero B, Schoenau E, Semler O.

J Musculoskelet Neuronal Interact. 2016 Mar;16(1):24-32.

15.

Involving Families with Osteogenesis Imperfecta in Health Service Research: Joint Development of the OI/ECE Questionnaire.

Dogba MJ, Dahan-Oliel N, Snider L, Glorieux FH, Durigova M, Palomo T, Cordey M, Bédard MH, Bedos C, Rauch F.

PLoS One. 2016 Jan 22;11(1):e0147654. doi: 10.1371/journal.pone.0147654. eCollection 2016.

16.

Value of rare low bone mass diseases for osteoporosis genetics.

Costantini A, Mäkitie O.

Bonekey Rep. 2016 Jan 6;5:773. doi: 10.1038/bonekey.2015.143. eCollection 2016. Review.

17.

The dentin phosphoprotein repeat region and inherited defects of dentin.

Yang J, Kawasaki K, Lee M, Reid BM, Nunez SM, Choi M, Seymen F, Koruyucu M, Kasimoglu Y, Estrella-Yuson N, Lin BP, Simmer JP, Hu JC.

Mol Genet Genomic Med. 2015 Sep 7;4(1):28-38. doi: 10.1002/mgg3.176. eCollection 2016 Jan.

18.

Sclerostin Antibody Treatment Improves the Bone Phenotype of Crtap(-/-) Mice, a Model of Recessive Osteogenesis Imperfecta.

Grafe I, Alexander S, Yang T, Lietman C, Homan EP, Munivez E, Chen Y, Jiang MM, Bertin T, Dawson B, Asuncion F, Ke HZ, Ominsky MS, Lee B.

J Bone Miner Res. 2016 May;31(5):1030-40. doi: 10.1002/jbmr.2776. Epub 2016 Feb 12.

19.

[Osteogenesis imperfecta: report of a case].

Hsayaoui N, Mbarki C, Melliti S, El Cadhi Y, Douik F, Mezghanni S, Oueslati H.

Pan Afr Med J. 2015 Jun 3;21:83. doi: 10.11604/pamj.2015.21.83.6416. eCollection 2015. French. No abstract available.

20.

Structure-mechanics relationships of collagen fibrils in the osteogenesis imperfecta mouse model.

Andriotis OG, Chang SW, Vanleene M, Howarth PH, Davies DE, Shefelbine SJ, Buehler MJ, Thurner PJ.

J R Soc Interface. 2015 Oct 6;12(111):20150701. doi: 10.1098/rsif.2015.0701.

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