Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 106

1.

Rare bone diseases and their dental, oral, and craniofacial manifestations.

Foster BL, Ramnitz MS, Gafni RI, Burke AB, Boyce AM, Lee JS, Wright JT, Akintoye SO, Somerman MJ, Collins MT.

J Dent Res. 2014 Jul;93(7 Suppl):7S-19S. doi: 10.1177/0022034514529150. Epub 2014 Apr 3. Review.

2.

Genetic disorders and bone affecting the craniofacial skeleton.

Chacon GE, Ugalde CM, Jabero MF.

Oral Maxillofac Surg Clin North Am. 2007 Nov;19(4):467-74, v. Review.

PMID:
18088898
3.

Molecular, phenotypic aspects and therapeutic horizons of rare genetic bone disorders.

Faruqi T, Dhawan N, Bahl J, Gupta V, Vohra S, Tu K, Abdelmagid SM.

Biomed Res Int. 2014;2014:670842. doi: 10.1155/2014/670842. Epub 2014 Oct 22. Review.

4.

Mild hypophosphatasia in utero: bent bones in a family with dental disease.

Comstock C, Bronsteen R, Lee W, Vettraino I.

J Ultrasound Med. 2005 May;24(5):707-9. No abstract available.

5.

Root anomalies and dentin dysplasia in autosomal recessive hyperphosphatemic familial tumoral calcinosis (HFTC).

Vieira AR, Lee M, Vairo F, Loguercio Leite JC, Munerato MC, Visioli F, D'Ávila SR, Wang SK, Choi M, Simmer JP, Hu JC.

Oral Surg Oral Med Oral Pathol Oral Radiol. 2015 Dec;120(6):e235-9. doi: 10.1016/j.oooo.2015.05.006. Epub 2015 May 28.

6.

Osteogenesis imperfecta and other heritable disorders of bone.

Paterson CR.

Baillieres Clin Endocrinol Metab. 1997 Apr;11(1):195-213. Review.

PMID:
9222492
7.

[FGF23 and skeletal metabolism].

Michigami T.

Clin Calcium. 2014 Jun;24(6):879-84. doi: CliCa1406879884. Review. Japanese.

PMID:
24870839
8.

Familial hypophosphatemic rickets.

Sattur A, Naikmasur VG, Shrivastava R, Babshet M.

J Indian Soc Pedod Prev Dent. 2010 Oct-Dec;28(4):302-6. doi: 10.4103/0970-4388.76163.

10.

[Vascular Calcification - Pathological Mechanism and Clinical Application - . Regulation of mineral metabolism and mineralization by FGF23].

Fukumoto S.

Clin Calcium. 2015 May;25(5):687-91. doi: CliCa1505687691. Review. Japanese.

PMID:
25926572
11.

GALNT3 gene mutation-associated chronic recurrent multifocal osteomyelitis and familial hyperphosphatemic familial tumoral calcinosis.

Demellawy DE, Chang N, de Nanassy J, Nasr A.

Scand J Rheumatol. 2015;44(2):170-2. doi: 10.3109/03009742.2014.958100. Epub 2014 Oct 29. No abstract available.

PMID:
25351881
12.

Hyperphosphatemic familial tumoral calcinosis: genetic models of deficient FGF23 action.

Folsom LJ, Imel EA.

Curr Osteoporos Rep. 2015 Apr;13(2):78-87. doi: 10.1007/s11914-015-0254-3. Review.

PMID:
25656441
13.

Inherited craniofacial fibrous dysplasia.

Pierce AM, Wilson DF, Goss AN.

Oral Surg Oral Med Oral Pathol. 1985 Oct;60(4):403-9.

PMID:
3864099
14.

Mineralization defects in cementum and craniofacial bone from loss of bone sialoprotein.

Foster BL, Ao M, Willoughby C, Soenjaya Y, Holm E, Lukashova L, Tran AB, Wimer HF, Zerfas PM, Nociti FH Jr, Kantovitz KR, Quan BD, Sone ED, Goldberg HA, Somerman MJ.

Bone. 2015 Sep;78:150-64. doi: 10.1016/j.bone.2015.05.007. Epub 2015 May 9.

15.

Familial craniofacial fibrous dysplasia: absence of linkage to GNAS1 and the gene for cherubism.

Mangion J, Edkins S, Goss AN, Stratton MR, Flanagan AM.

J Med Genet. 2000 Nov;37(11):E37. No abstract available.

16.

Clinical variability of familial tumoral calcinosis caused by novel GALNT3 mutations.

Ichikawa S, Baujat G, Seyahi A, Garoufali AG, Imel EA, Padgett LR, Austin AM, Sorenson AH, Pejin Z, Topouchian V, Quartier P, Cormier-Daire V, Dechaux M, Malandrinou FCh, Singhellakis PN, Le Merrer M, Econs MJ.

Am J Med Genet A. 2010 Apr;152A(4):896-903. doi: 10.1002/ajmg.a.33337.

17.

Development and Validation of a Simple Diagnostic Method to Detect Gain and Loss of Function Defects in Fibroblast Growth Factor-23.

Ramadan AR, Shawar SM, Alghamdi MA.

Horm Res Paediatr. 2016;86(1):45-52. doi: 10.1159/000447113. Epub 2016 Jun 30.

PMID:
27355663
18.

[Genetic basis for skeletal disease. Dental management of patients with bone diseases].

Shintani S, Ooshima T.

Clin Calcium. 2010 Aug;20(8):1259-65. doi: CliCa100812591265. Review. Japanese.

PMID:
20675938
19.

Gorham-Stout syndrome of the facial bones: a review of pathogenesis and treatment modalities and report of a case with a rare cutaneous manifestations.

Al-Jamali J, Glaum R, Kassem A, Voss PJ, Schmelzeisen R, Schön R.

Oral Surg Oral Med Oral Pathol Oral Radiol. 2012 Dec;114(6):e23-9. doi: 10.1016/j.oooo.2011.08.016. Epub 2012 May 12. Review.

PMID:
23159123
20.

Massive osteolysis (Gorham-Stout syndrome) in the maxillofacial region: an unusual manifestation.

Klein M, Metelmann HR, Gross U.

Int J Oral Maxillofac Surg. 1996 Oct;25(5):376-8.

PMID:
8961021

Supplemental Content

Support Center