BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

152 related articles for article (PubMed ID: 35354337)

  • 1. Postnatal Progressive Craniosynostosis in Syndromic Conditions: Two Patients With Saethre-Chotzen Due to
    Alawneh RJ; Johnson AL; Hoover-Fong JE; Jackson EM; Steinberg JP; MacCarrick G
    Cleft Palate Craniofac J; 2023 Aug; 60(8):1021-1028. PubMed ID: 35354337
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Reoperation for intracranial hypertension in TWIST1-confirmed Saethre-Chotzen syndrome: a 15-year review.
    Woods RH; Ul-Haq E; Wilkie AOM; Jayamohan J; Richards PG; Johnson D; Lester T; Wall SA
    Plast Reconstr Surg; 2009 Jun; 123(6):1801-1810. PubMed ID: 19483581
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Postnatal onset of craniosynostosis in a case of Saethre-Chotzen syndrome.
    de Heer IM; Hoogeboom J; Vermeij-Keers C; de Klein A; Vaandrager JM
    J Craniofac Surg; 2004 Nov; 15(6):1048-52. PubMed ID: 15547403
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatal diagnosis of a 7p15-p21 deletion encompassing the TWIST1 gene involved in Saethre-Chotzen syndrome.
    Spaggiari E; Aboura A; Sinico M; Mabboux P; Dupont C; Delezoide AL; Guimiot F
    Eur J Med Genet; 2012; 55(8-9):498-501. PubMed ID: 22569119
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical and genetic characteristics of craniosynostosis in Hungary.
    Bessenyei B; Nagy A; Szakszon K; Mokánszki A; Balogh E; Ujfalusi A; Tihanyi M; Novák L; Bognár L; Oláh É
    Am J Med Genet A; 2015 Dec; 167A(12):2985-91. PubMed ID: 26289989
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical and genetic analysis of patients with Saethre-Chotzen syndrome.
    de Heer IM; de Klein A; van den Ouweland AM; Vermeij-Keers C; Wouters CH; Vaandrager JM; Hovius SE; Hoogeboom JM
    Plast Reconstr Surg; 2005 Jun; 115(7):1894-902; discussion 1903-5. PubMed ID: 15923834
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Pharmacological targeting of KDM6A and KDM6B, as a novel therapeutic strategy for treating craniosynostosis in Saethre-Chotzen syndrome.
    Pribadi C; Camp E; Cakouros D; Anderson P; Glackin C; Gronthos S
    Stem Cell Res Ther; 2020 Dec; 11(1):529. PubMed ID: 33298158
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The natural history of patients treated for TWIST1-confirmed Saethre-Chotzen syndrome.
    Foo R; Guo Y; McDonald-McGinn DM; Zackai EH; Whitaker LA; Bartlett SP
    Plast Reconstr Surg; 2009 Dec; 124(6):2085-2095. PubMed ID: 19952666
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Saethre–Chotzen syndrome with an atypical phenotype: identification of TWIST microdeletion by array CGH.
    Cho E; Yang TH; Shin ES; Byeon JH; Kim GH; Eun BL
    Childs Nerv Syst; 2013 Nov; 29(11):2101-4. PubMed ID: 23958897
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Microdeletions of 5.5 Mb (4q13.2-q13.3) and 4.1 Mb (7p15.3-p21.1) associated with a saethre-chotzen-like phenotype, severe intellectual disability, and autism.
    Shimada S; Okamoto N; Nomura S; Fukui M; Shimakawa S; Sangu N; Shimojima K; Osawa M; Yamamoto T
    Am J Med Genet A; 2013 Aug; 161A(8):2078-83. PubMed ID: 23825006
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Contiguous gene deletion neighboring TWIST1 identified in a patient with Saethre-Chotzen syndrome associated with neurodevelopmental delay: Possible contribution of HDAC9.
    Shimbo H; Oyoshi T; Kurosawa K
    Congenit Anom (Kyoto); 2018 Jan; 58(1):33-35. PubMed ID: 28220539
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal diagnosis of craniosynostosis (compound Saethre-Chotzen syndrome phenotype) caused by a de novo complex chromosomal rearrangement (1; 4; 7) with a microdeletion of 7p21.3-7p15.3, including TWIST1 gene--a case report.
    Massalska D; Bijok J; Kucińska-Chahwan A; Jamsheer A; Bogdanowicz J; Jakiel G; Roszkowski T
    Ginekol Pol; 2014 Jul; 85(7):541-4. PubMed ID: 25118508
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Y-craniosynostosis by premature fusion of the metopic and coronal sutures: a new nosological entity or a variety of Saethre-Chotzen syndrome?
    di Rocco F; Benoit A; Vigneron J; Segura PB; Klein O; Collet C; Arnaud E
    Birth Defects Res A Clin Mol Teratol; 2015 Apr; 103(4):306-10. PubMed ID: 25808521
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Saethre-Chotzen syndrome: a case report].
    Díez de Los Ríos Quintanero B; Gracia Rojas E; Ortiz Movilla R; Cabrejas Núñez MJ; Marín Gabriel MÁ
    Arch Argent Pediatr; 2021 Apr; 119(2):e129-e132. PubMed ID: 33749202
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Disruption of TWIST1 translation by 5' UTR variants in Saethre-Chotzen syndrome.
    Zhou Y; Koelling N; Fenwick AL; McGowan SJ; Calpena E; Wall SA; Smithson SF; Wilkie AOM; Twigg SRF
    Hum Mutat; 2018 Oct; 39(10):1360-1365. PubMed ID: 30040876
    [TBL] [Abstract][Full Text] [Related]  

  • 16. New Pattern of Sutural Synostosis Associated With TWIST Gene Mutation and Saethre-Chotzen Syndrome: Peace Sign Synostosis.
    Tahiri Y; Bastidas N; McDonald-McGinn DM; Birgfeld C; Zackai EH; Taylor J; Bartlett SP
    J Craniofac Surg; 2015 Jul; 26(5):1564-7. PubMed ID: 26114524
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ablepharon and craniosynostosis in a patient with a localized TWIST1 basic domain substitution.
    Takenouchi T; Sakamoto Y; Sato H; Suzuki H; Uehara T; Ohsone Y; Kosaki K
    Am J Med Genet A; 2018 Dec; 176(12):2777-2780. PubMed ID: 30450715
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutations in snail family genes enhance craniosynostosis of Twist1 haplo-insufficient mice: implications for Saethre-Chotzen Syndrome.
    Oram KF; Gridley T
    Genetics; 2005 Jun; 170(2):971-4. PubMed ID: 15802514
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Saethre-Chotzen syndrome: a case report.
    Peña WA; Slavotinek A; Oberoi S
    Cleft Palate Craniofac J; 2010 May; 47(3):318-21. PubMed ID: 19860490
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic analysis of patients with the Saethre-Chotzen phenotype.
    Chun K; Teebi AS; Jung JH; Kennedy S; Laframboise R; Meschino WS; Nakabayashi K; Scherer SW; Ray PN; Teshima I
    Am J Med Genet; 2002 Jun; 110(2):136-43. PubMed ID: 12116251
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.