Format
Sort by

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 211

1.

Alendronate for the treatment of pediatric osteogenesis imperfecta: a randomized placebo-controlled study.

Ward LM, Rauch F, Whyte MP, D'Astous J, Gates PE, Grogan D, Lester EL, McCall RE, Pressly TA, Sanders JO, Smith PA, Steiner RD, Sullivan E, Tyerman G, Smith-Wright DL, Verbruggen N, Heyden N, Lombardi A, Glorieux FH.

J Clin Endocrinol Metab. 2011 Feb;96(2):355-64. doi: 10.1210/jc.2010-0636.

PMID:
21106710
2.

Characterising and treating osteogenesis imperfecta.

Bishop N.

Early Hum Dev. 2010 Nov;86(11):743-6. doi: 10.1016/j.earlhumdev.2010.08.002.

PMID:
20846798
3.

Mutations in FKBP10 cause recessive osteogenesis imperfecta and Bruck syndrome.

Kelley BP, Malfait F, Bonafe L, Baldridge D, Homan E, Symoens S, Willaert A, Elcioglu N, Van Maldergem L, Verellen-Dumoulin C, Gillerot Y, Napierala D, Krakow D, Beighton P, Superti-Furga A, De Paepe A, Lee B.

J Bone Miner Res. 2011 Mar;26(3):666-72. doi: 10.1002/jbmr.250.

4.

New drugs: Denosumab, dienogest/estradiol valerate, and polidocanol.

Hussar DA, Stevenson T.

J Am Pharm Assoc (2003). 2010 Sep-Oct;50(5):658-62. doi: 10.1331/JAPhA.2010.10536. No abstract available.

PMID:
20833626
5.

FKBP10 and Bruck syndrome: phenotypic heterogeneity or call for reclassification?

Shaheen R, Al-Owain M, Sakati N, Alzayed ZS, Alkuraya FS.

Am J Hum Genet. 2010 Aug 13;87(2):306-7; author reply 308. doi: 10.1016/j.ajhg.2010.05.020. No abstract available. Erratum in: Am J Hum Genet. 2010 Oct 8;87(4):571.

6.

Nanoscale morphology of Type I collagen is altered in the Brtl mouse model of Osteogenesis Imperfecta.

Wallace JM, Orr BG, Marini JC, Holl MM.

J Struct Biol. 2011 Jan;173(1):146-52. doi: 10.1016/j.jsb.2010.08.003.

7.

Cellular communications in bone homeostasis and repair.

Nakahama K.

Cell Mol Life Sci. 2010 Dec;67(23):4001-9. doi: 10.1007/s00018-010-0479-3. Review.

PMID:
20694737
8.

GH in combination with bisphosphonate treatment in osteogenesis imperfecta.

Antoniazzi F, Monti E, Venturi G, Franceschi R, Doro F, Gatti D, Zamboni G, Tatò L.

Eur J Endocrinol. 2010 Sep;163(3):479-87. doi: 10.1530/EJE-10-0208.

9.

Identification of a frameshift mutation in Osterix in a patient with recessive osteogenesis imperfecta.

Lapunzina P, Aglan M, Temtamy S, Caparrós-Martín JA, Valencia M, Letón R, Martínez-Glez V, Elhossini R, Amr K, Vilaboa N, Ruiz-Perez VL.

Am J Hum Genet. 2010 Jul 9;87(1):110-4. doi: 10.1016/j.ajhg.2010.05.016.

10.

Sclerostin: a gem from the genome leads to bone-building antibodies.

Paszty C, Turner CH, Robinson MK.

J Bone Miner Res. 2010 Sep;25(9):1897-904. doi: 10.1002/jbmr.161. Review. No abstract available.

11.

Generalized connective tissue disease in Crtap-/- mouse.

Baldridge D, Lennington J, Weis M, Homan EP, Jiang MM, Munivez E, Keene DR, Hogue WR, Pyott S, Byers PH, Krakow D, Cohn DH, Eyre DR, Lee B, Morello R.

PLoS One. 2010 May 11;5(5):e10560. doi: 10.1371/journal.pone.0010560.

12.

Osteogenesis imperfecta, normal collagen folding, and lack of cyclophilin B.

van Dijk FS, Cobben JM, Pals G.

N Engl J Med. 2010 May 20;362(20):1940-1; author reply 1941-2. doi: 10.1056/NEJMc1002797. No abstract available.

13.

A structure-activity relationship study elucidating the mechanism of sequence-specific collagen recognition by the chaperone HSP47.

Nishikawa Y, Takahara Y, Asada S, Shigenaga A, Otaka A, Kitagawa K, Koide T.

Bioorg Med Chem. 2010 Jun 1;18(11):3767-75. doi: 10.1016/j.bmc.2010.04.054.

PMID:
20471275
14.

Amelioration of a mouse model of osteogenesis imperfecta with hematopoietic stem cell transplantation: microcomputed tomography studies.

Mehrotra M, Rosol M, Ogawa M, Larue AC.

Exp Hematol. 2010 Jul;38(7):593-602. doi: 10.1016/j.exphem.2010.04.008.

15.

Dentinogenesis imperfecta in children with osteogenesis imperfecta: a clinical and ultrastructural study.

Majorana A, Bardellini E, Brunelli PC, Lacaita M, Cazzolla AP, Favia G.

Int J Paediatr Dent. 2010 Mar;20(2):112-8. doi: 10.1111/j.1365-263X.2010.01033.x.

PMID:
20384825
16.

Prolyl 3-hydroxylase 1 null mice display abnormalities in fibrillar collagen-rich tissues such as tendons, skin, and bones.

Vranka JA, Pokidysheva E, Hayashi L, Zientek K, Mizuno K, Ishikawa Y, Maddox K, Tufa S, Keene DR, Klein R, Bächinger HP.

J Biol Chem. 2010 May 28;285(22):17253-62. doi: 10.1074/jbc.M110.102228. Erratum in: J Biol Chem. 2010 Jun 25;285(26):20421.

17.

Mutations in the gene encoding the RER protein FKBP65 cause autosomal-recessive osteogenesis imperfecta.

Alanay Y, Avaygan H, Camacho N, Utine GE, Boduroglu K, Aktas D, Alikasifoglu M, Tuncbilek E, Orhan D, Bakar FT, Zabel B, Superti-Furga A, Bruckner-Tuderman L, Curry CJ, Pyott S, Byers PH, Eyre DR, Baldridge D, Lee B, Merrill AE, Davis EC, Cohn DH, Akarsu N, Krakow D.

Am J Hum Genet. 2010 Apr 9;86(4):551-9. doi: 10.1016/j.ajhg.2010.02.022. Erratum in: Am J Hum Genet. 2010 Oct 8;87(4):572-3.

18.

Immature osteoblast lineage cells increase osteoclastogenesis in osteogenesis imperfecta murine.

Li H, Jiang X, Delaney J, Franceschetti T, Bilic-Curcic I, Kalinovsky J, Lorenzo JA, Grcevic D, Rowe DW, Kalajzic I.

Am J Pathol. 2010 May;176(5):2405-13. doi: 10.2353/ajpath.2010.090704.

19.

Homozygosity for a missense mutation in SERPINH1, which encodes the collagen chaperone protein HSP47, results in severe recessive osteogenesis imperfecta.

Christiansen HE, Schwarze U, Pyott SM, AlSwaid A, Al Balwi M, Alrasheed S, Pepin MG, Weis MA, Eyre DR, Byers PH.

Am J Hum Genet. 2010 Mar 12;86(3):389-98. doi: 10.1016/j.ajhg.2010.01.034.

20.

Lack of cyclophilin B in osteogenesis imperfecta with normal collagen folding.

Barnes AM, Carter EM, Cabral WA, Weis M, Chang W, Makareeva E, Leikin S, Rotimi CN, Eyre DR, Raggio CL, Marini JC.

N Engl J Med. 2010 Feb 11;362(6):521-8. doi: 10.1056/NEJMoa0907705.

Items per page

Supplemental Content

Support Center