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Results: 1 to 20 of 97

Similar articles for PubMed (Select 24663682)

1.

Dental Anomalies Associated with Craniometaphyseal Dysplasia.

Chen IP, Tadinada A, Dutra EH, Utreja A, Uribe F, Reichenberger EJ.

J Dent Res. 2014 Mar 24;93(6):553-558. [Epub ahead of print]

2.

Introduction of a Phe377del mutation in ANK creates a mouse model for craniometaphyseal dysplasia.

Chen IP, Wang CJ, Strecker S, Koczon-Jaremko B, Boskey A, Reichenberger EJ.

J Bone Miner Res. 2009 Jul;24(7):1206-15. doi: 10.1359/jbmr.090218.

3.

A Phe377del mutation in ANK leads to impaired osteoblastogenesis and osteoclastogenesis in a mouse model for craniometaphyseal dysplasia (CMD).

Chen IP, Wang L, Jiang X, Aguila HL, Reichenberger EJ.

Hum Mol Genet. 2011 Mar 1;20(5):948-61. doi: 10.1093/hmg/ddq541. Epub 2010 Dec 13.

4.

Dental abnormalities in a mouse model for craniometaphyseal dysplasia.

Dutra EH, Chen IP, Reichenberger EJ.

J Dent Res. 2013 Feb;92(2):173-9. doi: 10.1177/0022034512468157. Epub 2012 Nov 15.

5.

Craniometaphyseal Dysplasia, Autosomal Dominant.

Reichenberger E, Chen IP.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Dolan CR, Fong CT, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2015.
2007 Aug 27 [updated 2015 Jan 15].

6.

Dental anomalies in a child with craniometaphysial dysplasia.

Zhang H, Somerman MJ, Berg J, Cunningham ML, Williams B.

Pediatr Dent. 2007 Sep-Oct;29(5):415-9.

PMID:
18027777
7.

Tooth eruption in a patient with craniometaphyseal dysplasia: case report.

Hayashibara T, Komura T, Sobue S, Ooshima T.

J Oral Pathol Med. 2000 Oct;29(9):460-2.

PMID:
11016689
8.

Heterozygous mutations in ANKH, the human ortholog of the mouse progressive ankylosis gene, result in craniometaphyseal dysplasia.

Nürnberg P, Thiele H, Chandler D, Höhne W, Cunningham ML, Ritter H, Leschik G, Uhlmann K, Mischung C, Harrop K, Goldblatt J, Borochowitz ZU, Kotzot D, Westermann F, Mundlos S, Braun HS, Laing N, Tinschert S.

Nat Genet. 2001 May;28(1):37-41.

PMID:
11326272
9.

Variability of the cranial and dental phenotype in Williams syndrome.

Axelsson S.

Swed Dent J Suppl. 2005;(170):3-67.

PMID:
15762376
10.

A novel autosomal recessive GJA1 missense mutation linked to Craniometaphyseal dysplasia.

Hu Y, Chen IP, de Almeida S, Tiziani V, Do Amaral CM, Gowrishankar K, Passos-Bueno MR, Reichenberger EJ.

PLoS One. 2013 Aug 12;8(8):e73576. doi: 10.1371/journal.pone.0073576. eCollection 2013.

11.

Craniometaphyseal dysplasia associated with obstructive sleep apnoea syndrome.

Mintz S, Velez I.

Dentomaxillofac Radiol. 2004 Jul;33(4):262-6. Review.

PMID:
15533982
12.

Induced pluripotent stem cell reprogramming by integration-free Sendai virus vectors from peripheral blood of patients with craniometaphyseal dysplasia.

Chen IP, Fukuda K, Fusaki N, Iida A, Hasegawa M, Lichtler A, Reichenberger EJ.

Cell Reprogram. 2013 Dec;15(6):503-13. doi: 10.1089/cell.2013.0037. Epub 2013 Nov 12.

13.

Autosomal dominant craniometaphyseal dysplasia with atypical features.

McKay DR, Fialkov JA.

Br J Plast Surg. 2002 Mar;55(2):144-8.

PMID:
11987949
14.

Biochemical and genetic analysis of ANK in arthritis and bone disease.

Gurley KA, Reimer RJ, Kingsley DM.

Am J Hum Genet. 2006 Dec;79(6):1017-29. Epub 2006 Oct 16.

15.

Craniofacial surgery for craniometaphyseal dysplasia.

Ahmad FU, Mahapatra AK, Mahajan H.

Neurol India. 2006 Mar;54(1):97-9.

16.

Intracranial hypertension in two cases of craniometaphyseal dysplasia: differing surgical options.

Rivero-Garvía M, Márquez-Rivas FJ, García-Iglesias A, Gutiérrez-González R.

Neurosurg Focus. 2011 Aug;31(2):E6. doi: 10.3171/2011.4.FOCUS1126.

PMID:
21806345
17.

Craniometaphyseal dysplasia: a case report.

Lamazza L, Messina A, D'Ambrosio F, Spink M, De Biase A.

Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2009 May;107(5):e23-7. doi: 10.1016/j.tripleo.2009.01.049.

PMID:
19426903
18.

Three novel mutations in the ANK membrane protein cause craniometaphyseal dysplasia with variable conductive hearing loss.

Kornak U, Brancati F, Le Merrer M, Lichtenbelt K, Höhne W, Tinschert S, Garaci FG, Dallapiccola B, Nürnberg P.

Am J Med Genet A. 2010 Apr;152A(4):870-4. doi: 10.1002/ajmg.a.33301.

PMID:
20358596
19.

Cerebellomedullary compression in recessive craniometaphyseal dysplasia.

Boltshauser E, Schmitt B, Wichmann W, Valavanis A, Sailer H, Yonekawa Y.

Neuroradiology. 1996 May;38 Suppl 1:S193-5.

PMID:
8811714
20.

Foramen magnum decompression and expansile duroplasty for acquired Chiari type I malformation in craniometaphyseal dysplasia.

Sewell MD, Akram H, Wadley J.

Br J Neurosurg. 2008 Feb;22(1):83-5. doi: 10.1080/02688690701658737.

PMID:
18224526
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