These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
170 related items for PubMed ID: 36936765
21. Cleidocranial dysplasia: importance of radiographic images in diagnosis of the condition. Tanaka JL, Ono E, Filho EM, Castilho JC, Moraes LC, Moraes ME. J Oral Sci; 2006 Sep; 48(3):161-6. PubMed ID: 17023750 [Abstract] [Full Text] [Related]
22. [Analysis of root resorption and dental structure in patients with cleidocranial dysplasia]. Yang X, Zhang Cy, Zheng Sg. Beijing Da Xue Xue Bao Yi Xue Ban; 2011 Feb 18; 43(1):98-101. PubMed ID: 21321630 [Abstract] [Full Text] [Related]
23. RUNX2 Nonsense Mutation Associated with Cleidocranial Dysplasia with Unusual Dental Features. Barbosa Lima R, de Souza Furtado TC, Nelson-Filho P, Assed Bezerra da Silva R, Wanderley Garcia Paula-Silva F, Kitazono de Carvalho F, Mussolino de Queiroz A. J Dent Child (Chic); 2022 May 15; 89(2):126-129. PubMed ID: 35986479 [Abstract] [Full Text] [Related]
24. A Case of Cleidocranial Dysplasia with a Novel Mutation and Growth Velocity Gain with Growth Hormone Treatment. Çamtosun E, Akıncı A, Demiral E, Tekedereli İ, Sığırcı A. J Clin Res Pediatr Endocrinol; 2019 Sep 03; 11(3):301-305. PubMed ID: 30468148 [Abstract] [Full Text] [Related]
25. [Orthodontic and oral surgery therapy in cleidocranial dysplasia]. Balaton G, Tarján I, Balaton P, Barabási Z, Gyulai Gál S, Nagy K, Vajó Z. Fogorv Sz; 2007 Feb 03; 100(1):17-21. PubMed ID: 17444132 [Abstract] [Full Text] [Related]
26. RUNX2 mutations in cleidocranial dysplasia patients. Ryoo HM, Kang HY, Lee SK, Lee KE, Kim JW. Oral Dis; 2010 Jan 03; 16(1):55-60. PubMed ID: 19744171 [Abstract] [Full Text] [Related]
27. Detection and diagnosis of cleidocranial dysplasia by panoramic radiography: a retrospective study. Shi Y, Ye Z, Liu Y, Wang H, You M. BMC Oral Health; 2022 Dec 01; 22(1):558. PubMed ID: 36456973 [Abstract] [Full Text] [Related]
28. Cleidocranial dysplasia with hearing loss. Candamourty R, Venkatachalam S, Yuvaraj V, Kumar GS. J Nat Sci Biol Med; 2013 Jan 01; 4(1):245-9. PubMed ID: 23633875 [Abstract] [Full Text] [Related]
29. Cementum analysis in cleidocranial dysostosis. Manjunath K, Kavitha B, Saraswathi TR, Sivapathasundharam B, Manikandhan R. Indian J Dent Res; 2008 Jan 01; 19(3):253-6. PubMed ID: 18797104 [Abstract] [Full Text] [Related]
30. Cleidocranial dysplasia: maxillary alterations on the transverse plane. Presence of crown-radicular anomalies and multidisciplinary approach of a clinical case. Romeo U, Galluccio G, Palaia G, Tenore G, Carpenteri F, Barbato E, Polimeni A. Oral Health Dent Manag; 2014 Jun 01; 13(2):529-35. PubMed ID: 24984677 [Abstract] [Full Text] [Related]
31. Cleidocranial dysplasia: a family report. Chelvan HT, Malathi N, Kailasam V, Ponnudurai A. J Indian Soc Pedod Prev Dent; 2009 Jun 01; 27(4):249-52. PubMed ID: 19915277 [Abstract] [Full Text] [Related]
32. Molecular Genetics of Cleidocranial Dysplasia. Motaei J, Salmaninejad A, Jamali E, Khorsand I, Ahmadvand M, Shabani S, Karimi F, Nazari MS, Ketabchi G, Naqipour F. Fetal Pediatr Pathol; 2021 Oct 01; 40(5):442-454. PubMed ID: 31984822 [Abstract] [Full Text] [Related]
33. A case of Japanese cleidocranial dysplasia with a CBFA1 frameshift mutation. Yokozeki M, Ohyama K, Tsuji M, Goseki-Sone M, Oida S, Orimo H, Moriyama K, Kuroda T. J Craniofac Genet Dev Biol; 2000 Oct 01; 20(3):121-6. PubMed ID: 11321596 [Abstract] [Full Text] [Related]
34. Cleidocranial dysplasia. Zabeen B, Mohsin F, Taher A, Khan M, Azad K, Nahar N. Mymensingh Med J; 2008 Jan 01; 17(1):82-4. PubMed ID: 18285740 [Abstract] [Full Text] [Related]
35. A rare case of cleidocranial dysplasia presenting with failure to thrive. Mahajan PS, Mahajan AP, Mahajan PS. J Nat Sci Biol Med; 2015 Jan 01; 6(1):232-5. PubMed ID: 25810671 [Abstract] [Full Text] [Related]
36. Effect of cleidocranial dysplasia-related novel mutation of RUNX2 on characteristics of dental pulp cells and tooth development. Xuan D, Sun X, Yan Y, Xie B, Xu P, Zhang J. J Cell Biochem; 2010 Dec 15; 111(6):1473-81. PubMed ID: 20872798 [Abstract] [Full Text] [Related]
37. Functional analysis of RUNX2 mutations in Japanese patients with cleidocranial dysplasia demonstrates novel genotype-phenotype correlations. Yoshida T, Kanegane H, Osato M, Yanagida M, Miyawaki T, Ito Y, Shigesada K. Am J Hum Genet; 2002 Oct 15; 71(4):724-38. PubMed ID: 12196916 [Abstract] [Full Text] [Related]
38. RUNX2 gene status in a cleidocranial dysplasia patient without supernumerary teeth. Anthonappa RP, King NM, Mahmoud Rabie AB. J Investig Clin Dent; 2013 May 15; 4(2):124-7. PubMed ID: 23188595 [Abstract] [Full Text] [Related]
39. Comparison of mesenchymal-like stem/progenitor cells derived from supernumerary teeth with stem cells from human exfoliated deciduous teeth. Lee S, An S, Kang TH, Kim KH, Chang NH, Kang S, Kwak CK, Park HS. Regen Med; 2011 Nov 15; 6(6):689-99. PubMed ID: 22050521 [Abstract] [Full Text] [Related]
40. Titanium screw anchorage for traction of many impacted teeth in a patient with cleidocranial dysplasia. Kuroda S, Yanagita T, Kyung HM, Takano-Yamamoto T. Am J Orthod Dentofacial Orthop; 2007 May 15; 131(5):666-9. PubMed ID: 17482089 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]