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Results: 1 to 20 of 21

1.

Long term follow-up of four patients with Keutel syndrome.

Khosroshahi HE, Sahin SC, Akyuz Y, Ede H.

Am J Med Genet A. 2014 Nov;164A(11):2849-56. doi: 10.1002/ajmg.a.36699. Epub 2014 Aug 13.

2.

Keutel syndrome: report of two novel MGP mutations and discussion of clinical overlap with arylsulfatase E deficiency and relapsing polychondritis.

Weaver KN, El Hallek M, Hopkin RJ, Sund KL, Henrickson M, Del Gaudio D, Yuksel A, Acar GO, Bober MB, Kim J, Boyadjiev SA.

Am J Med Genet A. 2014 Apr;164A(4):1062-8. doi: 10.1002/ajmg.a.36390. Epub 2014 Jan 23.

PMID:
24458983
3.

[Keutel syndrome with tracheal stenosis as the major symptom: case report and literature review].

Sun LF, Ju YF, Fu GJ, Wang JR, Feng YZ, Chen X.

Zhonghua Er Ke Za Zhi. 2013 Jul;51(7):527-30. Review. Chinese.

PMID:
24267135
4.

Neuroimaging findings in children with Keutel syndrome.

Bosemani T, Felling RJ, Wyse E, Pearl MS, Tekes A, Ahn E, Poretti A, Huisman TA.

Pediatr Radiol. 2014 Jan;44(1):73-8. doi: 10.1007/s00247-013-2768-0. Epub 2013 Aug 7.

PMID:
23917590
5.

Elastin haploinsufficiency impedes the progression of arterial calcification in MGP-deficient mice.

Khavandgar Z, Roman H, Li J, Lee S, Vali H, Brinckmann J, Davis EC, Murshed M.

J Bone Miner Res. 2014 Feb;29(2):327-37. doi: 10.1002/jbmr.2039.

PMID:
23857752
6.

[A case of Keutel syndrome in child (review the literature)].

Xu L, Xia Z, Liu X, Huang S.

Lin Chung Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2012 Sep;26(18):793-4. Review. Chinese.

PMID:
23259292
7.

Mechanisms of arterial remodeling: lessons from genetic diseases.

van Varik BJ, Rennenberg RJ, Reutelingsperger CP, Kroon AA, de Leeuw PW, Schurgers LJ.

Front Genet. 2012 Dec 13;3:290. doi: 10.3389/fgene.2012.00290. eCollection 2012.

8.

Circulating matrix γ-carboxyglutamate protein (MGP) species are refractory to vitamin K treatment in a new case of Keutel syndrome.

Cranenburg EC, VAN Spaendonck-Zwarts KY, Bonafe L, Mittaz Crettol L, Rödiger LA, Dikkers FG, VAN Essen AJ, Superti-Furga A, Alexandrakis E, Vermeer C, Schurgers LJ, Laverman GD.

J Thromb Haemost. 2011 Jun;9(6):1225-35. doi: 10.1111/j.1538-7836.2011.04263.x.

PMID:
21435166
9.

Keutel syndrome in a patient presenting with hearing loss.

Acar GO, Yilmaz M, Sekercioğlu N, Yüksel A.

B-ENT. 2010;6(3):201-4.

PMID:
21090163
10.

Idiopathic isolated laryngotracheobronchial cartilage calcification in a child.

Ceyhan M, Nural MS, Elmali M, Bayrak IK.

Clin Imaging. 2008 Jan-Feb;32(1):51-3. doi: 10.1016/j.clinimag.2007.04.026.

PMID:
18164396
11.

Tracheobronchial calcification associated with Keutel syndrome.

Ozdemir N, Ersu R, Akalin F, Karadag B, Kut A, Karakoç F, Elçioglu N, Dagli E.

Turk J Pediatr. 2006 Oct-Dec;48(4):357-61.

12.

Petrified ears in a patient with Keutel syndrome: temporal bone CT findings.

Parmar H, Blaser S, Unger S, Yoo SJ, Papsin B.

Pediatr Radiol. 2006 Mar;36(3):241-3. Epub 2005 Nov 18.

PMID:
16328322
13.

A novel MGP mutation in a consanguineous family: review of the clinical and molecular characteristics of Keutel syndrome.

Hur DJ, Raymond GV, Kahler SG, Riegert-Johnson DL, Cohen BA, Boyadjiev SA.

Am J Med Genet A. 2005 May 15;135(1):36-40. Review.

PMID:
15810001
14.

Brachytelephalangy with sparing of the fifth distal phalanx: a feature highly suggestive of Keutel syndrome.

Miller SF.

Pediatr Radiol. 2003 Mar;33(3):186-9. Epub 2002 Dec 19. Review.

PMID:
12612818
15.

Tracheobronchial stenosis in Keutel syndrome.

Meier M, Weng LP, Alexandrakis E, Rüschoff J, Goeckenjan G.

Eur Respir J. 2001 Mar;17(3):566-9.

16.

Mutations in the gene encoding the human matrix Gla protein cause Keutel syndrome.

Munroe PB, Olgunturk RO, Fryns JP, Van Maldergem L, Ziereisen F, Yuksel B, Gardiner RM, Chung E.

Nat Genet. 1999 Jan;21(1):142-4.

PMID:
9916809
17.

Keutel syndrome: further characterization and review.

Teebi AS, Lambert DM, Kaye GM, Al-Fifi S, Tewfik TL, Azouz EM.

Am J Med Genet. 1998 Jun 30;78(2):182-7. Review.

PMID:
9674914
18.

Premature tracheobronchial, laryngeal and costochondral cartilage calcification in children.

Haddad MC, Sharif HS, Jared MS, Sammak BM, al Shahed MS.

Clin Radiol. 1993 Jan;47(1):52-5.

PMID:
8428419
19.

The Keutel syndrome. Report of a case and review of the literature.

Ziereisen F, De Munter C, Perlmutter N.

Pediatr Radiol. 1993;23(4):314-5. Review.

PMID:
8414764
20.

Keutel syndrome: clinical report and literature review.

Cormode EJ, Dawson M, Lowry RB.

Am J Med Genet. 1986 Jun;24(2):289-94.

PMID:
3717211
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