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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

131 related articles for article (PubMed ID: 24267135)

  • 1. [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. PubMed ID: 24267135
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A case of Keutel syndrome diagnosed in the neonatal period: associated with Binder phenotype.
    Demirel G; Oguz SS; Celik IH; Erdeve O; Uras N; Dilmen U
    Genet Couns; 2012; 23(1):25-30. PubMed ID: 22611639
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 48(4):357-61. PubMed ID: 17290573
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [A case of Keutel syndrome in child (review the literature)].
    Xu L; Xia Z; Liu X; Huang S
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2012 Sep; 26(18):793-4. PubMed ID: 23259292
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Tracheobronchial stenosis in Keutel syndrome.
    Sun LF; Chen X
    Indian Pediatr; 2012 Sep; 49(9):759. PubMed ID: 23024086
    [No Abstract]   [Full Text] [Related]  

  • 6. 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. PubMed ID: 8414764
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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. PubMed ID: 12612818
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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. PubMed ID: 23917590
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A rare cause of dyspnea in emergency medicine: Keutel syndrome.
    Bayramoğlu A; Saritemur M; Tasdemir S; Omeroglu M; Erdem HB; Sahin I
    Am J Emerg Med; 2016 May; 34(5):935.e3-5. PubMed ID: 26462901
    [No Abstract]   [Full Text] [Related]  

  • 10. Keutel syndrome in a patient presenting with hearing loss.
    Acar GO; Yilmaz M; Sekercioğlu N; Yüksel A
    B-ENT; 2010; 6(3):201-4. PubMed ID: 21090163
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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. PubMed ID: 25123378
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Tracheobronchial Tree Ossification in a 5-Year-Old Boy with Keutel Syndrome: A Case Report.
    Shabanian R; Amiri A; Elmi S; Sheykhian T
    J Tehran Heart Cent; 2022 Jul; 17(3):152-155. PubMed ID: 37252084
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Tracheobronchial stenosis in Keutel syndrome.
    Meier M; Weng LP; Alexandrakis E; Rüschoff J; Goeckenjan G
    Eur Respir J; 2001 Mar; 17(3):566-9. PubMed ID: 11405537
    [TBL] [Abstract][Full Text] [Related]  

  • 14. CLINICAL VARIABILITY IN TWO SISTERS WITH KEUTEL SYNDROME DUE TO A HOMOZYGOUS MUTATION IN MGP GENE.
    Tüysüz B; Cinar B; Laçiner S; Onay H; Mittaz-Crettol L
    Genet Couns; 2015; 26(2):187-94. PubMed ID: 26349188
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Keutel syndrome: clinical report and literature review.
    Cormode EJ; Dawson M; Lowry RB
    Am J Med Genet; 1986 Jun; 24(2):289-94. PubMed ID: 3717211
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 78(2):182-7. PubMed ID: 9674914
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Keutel syndrome: a report of four cases.
    Khosroshahi HE; Uluoğlu O; Olguntürk R; Başaklar C
    Eur J Pediatr; 1989 Dec; 149(3):188-91. PubMed ID: 2515061
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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. PubMed ID: 16328322
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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. PubMed ID: 8428419
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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. PubMed ID: 24458983
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.