304 related articles for article (PubMed ID: 24700690)
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. PubMed ID: 24700690
[TBL] [Abstract][Full Text] [Related]
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. PubMed ID: 18088898
[TBL] [Abstract][Full Text] [Related]
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. PubMed ID: 25530967
[TBL] [Abstract][Full Text] [Related]
4. Recessive mutation in GALNT3 causes hyperphosphatemic familial tumoral calcinosis associated with chronic recurrent multifocal osteomyelitis.
Albaramki J; Dmour H; Shboul M; Bonnard C; Venkatesh B; Odeh R
Turk J Pediatr; 2019; 61(1):130-133. PubMed ID: 31559735
[TBL] [Abstract][Full Text] [Related]
5. Hyperphosphatemic familial tumoral calcinosis secondary to fibroblast growth factor 23 (FGF23) mutation: a report of two affected families and review of the literature.
Chakhtoura M; Ramnitz MS; Khoury N; Nemer G; Shabb N; Abchee A; Berberi A; Hourani M; Collins M; Ichikawa S; El Hajj Fuleihan G
Osteoporos Int; 2018 Sep; 29(9):1987-2009. PubMed ID: 29923062
[TBL] [Abstract][Full Text] [Related]
6. Dental and craniofacial defects in the Crtap
Xu H; Lenhart SA; Chu EY; Chavez MB; Wimer HF; Dimori M; Somerman MJ; Morello R; Foster BL; Hatch NE
Dev Dyn; 2020 Jul; 249(7):884-897. PubMed ID: 32133710
[TBL] [Abstract][Full Text] [Related]
7. 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. PubMed ID: 15840803
[No Abstract] [Full Text] [Related]
8. 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. PubMed ID: 26337219
[TBL] [Abstract][Full Text] [Related]
9. Dental Manifestations of Pediatric Bone Disorders.
Yepes JF
Curr Osteoporos Rep; 2017 Dec; 15(6):588-592. PubMed ID: 28965204
[TBL] [Abstract][Full Text] [Related]
10. Phenotypic and Genotypic Characterization and Treatment of a Cohort With Familial Tumoral Calcinosis/Hyperostosis-Hyperphosphatemia Syndrome.
Ramnitz MS; Gourh P; Goldbach-Mansky R; Wodajo F; Ichikawa S; Econs MJ; White KE; Molinolo A; Chen MY; Heller T; Del Rivero J; Seo-Mayer P; Arabshahi B; Jackson MB; Hatab S; McCarthy E; Guthrie LC; Brillante BA; Gafni RI; Collins MT
J Bone Miner Res; 2016 Oct; 31(10):1845-1854. PubMed ID: 27164190
[TBL] [Abstract][Full Text] [Related]
11. Osteogenesis imperfecta and other heritable disorders of bone.
Paterson CR
Baillieres Clin Endocrinol Metab; 1997 Apr; 11(1):195-213. PubMed ID: 9222492
[TBL] [Abstract][Full Text] [Related]
12. [FGF23 and skeletal metabolism].
Michigami T
Clin Calcium; 2014 Jun; 24(6):879-84. PubMed ID: 24870839
[TBL] [Abstract][Full Text] [Related]
13. Hyperphosphatemic Familial Tumoral Calcinosis in Two Siblings with a Novel Mutation in
Kışla Ekinci RM; Gürbüz F; Balcı S; Bişgin A; Taştan M; Yüksel B; Yılmaz M
J Clin Res Pediatr Endocrinol; 2019 Feb; 11(1):94-99. PubMed ID: 30015621
[TBL] [Abstract][Full Text] [Related]
14. 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. PubMed ID: 25351881
[No Abstract] [Full Text] [Related]
15. Familial hypophosphatemic rickets.
Sattur A; Naikmasur VG; Shrivastava R; Babshet M
J Indian Soc Pedod Prev Dent; 2010; 28(4):302-6. PubMed ID: 21273721
[TBL] [Abstract][Full Text] [Related]
16. Hereditary dentin defects with systemic diseases.
Su T; Zhu Y; Wang X; Zhu Q; Duan X
Oral Dis; 2023 Sep; 29(6):2376-2393. PubMed ID: 37094075
[TBL] [Abstract][Full Text] [Related]
17. [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. PubMed ID: 25926572
[TBL] [Abstract][Full Text] [Related]
18. A Large Skull Defect Due to Gorham-Stout Disease: Case Report and Literature Review on Pathogenesis, Diagnosis, and Treatment.
de Keyser CE; Saltzherr MS; Bos EM; Zillikens MC
Front Endocrinol (Lausanne); 2020; 11():37. PubMed ID: 32117063
[TBL] [Abstract][Full Text] [Related]
19. Hyperphosphataemic familial tumoral calcinosis: case report of a rare and challenging disease.
Guerra MG; Videira T; de Fonseca D; Vieira R; Dos Santos J; Pinto S
Scand J Rheumatol; 2020 Jan; 49(1):80-81. PubMed ID: 31213107
[No Abstract] [Full Text] [Related]
20. Hyperphosphatemic familial tumoral calcinosis: genetic models of deficient FGF23 action.
Folsom LJ; Imel EA
Curr Osteoporos Rep; 2015 Apr; 13(2):78-87. PubMed ID: 25656441
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]