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Journal Abstract Search

175 related items for PubMed ID: 15131704

  • 1. [Complex craniofacial synostoses].
    Meling TR, Ørstavik KH, Heiberg A.
    Tidsskr Nor Laegeforen; 2004 May 06; 124(9):1230-4. PubMed ID: 15131704
    [Abstract] [Full Text] [Related]

  • 2. [Genetics of craniofacial development].
    van Adrichem LN, Hoogeboom AJ, Wolvius EB.
    Ned Tijdschr Tandheelkd; 2008 Feb 06; 115(2):61-8. PubMed ID: 18326400
    [Abstract] [Full Text] [Related]

  • 3. Preoperative anthropometric dysmorphology in metopic synostosis.
    Kolar JC, Salter EM.
    Am J Phys Anthropol; 1997 Jul 06; 103(3):341-51. PubMed ID: 9261497
    [Abstract] [Full Text] [Related]

  • 4. [Etiological and pathogenetic mechanisms in development of craniosynostoses in children].
    Ovchinnikov SN, Severgina ES, Lopatin AV.
    Arkh Patol; 2003 Jul 06; 65(3):54-8. PubMed ID: 12879617
    [Abstract] [Full Text] [Related]

  • 5. Coronal synostosis syndrome (Muenke syndrome): the value of genetic testing versus clinical diagnosis.
    Ranger A, Chaudhary N, Rau J, Matir D, Goobie S.
    J Craniofac Surg; 2011 Jan 06; 22(1):187-90. PubMed ID: 21233754
    [Abstract] [Full Text] [Related]

  • 6. Fibroblast growth factor receptor mutational screening in newborns affected by metopic synostosis.
    Tartaglia M, Bordoni V, Velardi F, Basile RT, Saulle E, Tenconi R, Di Rocco C, Battaglia PA.
    Childs Nerv Syst; 1999 Aug 06; 15(8):389-93; discussion 393-4. PubMed ID: 10447608
    [Abstract] [Full Text] [Related]

  • 7. Phenotypic diversity in patients with craniosynostoses unrelated to Apert syndrome: the role of fibroblast growth factor receptor gene mutations.
    Ito S, Sekido K, Kanno H, Sato H, Tanaka M, Yamaguchi K, Yamamoto I.
    J Neurosurg; 2005 Jan 06; 102(1 Suppl):23-30. PubMed ID: 16206730
    [Abstract] [Full Text] [Related]

  • 8. [Premature craniosynostosis. Diagnosis and treatment].
    Tange MR, Midholm S, Sindet-Petersen S, Christensen L.
    Ugeskr Laeger; 1994 Mar 07; 156(10):1459-65. PubMed ID: 8016932
    [Abstract] [Full Text] [Related]

  • 9. A Pro253Arg mutation in fibroblast growth factor receptor 2 (Fgfr2) causes skeleton malformation mimicking human Apert syndrome by affecting both chondrogenesis and osteogenesis.
    Yin L, Du X, Li C, Xu X, Chen Z, Su N, Zhao L, Qi H, Li F, Xue J, Yang J, Jin M, Deng C, Chen L.
    Bone; 2008 Apr 07; 42(4):631-43. PubMed ID: 18242159
    [Abstract] [Full Text] [Related]

  • 10. The molecular pathology of syndromic craniosynostosis.
    Reardon W, Winter RM.
    Mol Med Today; 1995 Dec 07; 1(9):432-7. PubMed ID: 9415192
    [Abstract] [Full Text] [Related]

  • 11. Role of the extracellular matrix and growth factors in skull morphogenesis and in the pathogenesis of craniosynostosis.
    Carinci P, Becchetti E, Bodo M.
    Int J Dev Biol; 2000 Dec 07; 44(6):715-23. PubMed ID: 11061436
    [Abstract] [Full Text] [Related]

  • 12. Facial suture synostosis of newborn Fgfr1(P250R/+) and Fgfr2(S252W/+) mouse models of Pfeiffer and Apert syndromes.
    Purushothaman R, Cox TC, Maga AM, Cunningham ML.
    Birth Defects Res A Clin Mol Teratol; 2011 Jul 07; 91(7):603-9. PubMed ID: 21538817
    [Abstract] [Full Text] [Related]

  • 13. Genetics of craniosynostosis.
    Kimonis V, Gold JA, Hoffman TL, Panchal J, Boyadjiev SA.
    Semin Pediatr Neurol; 2007 Sep 07; 14(3):150-61. PubMed ID: 17980312
    [Abstract] [Full Text] [Related]

  • 14. Quantitative evaluation of facial hypoplasia and airway obstruction in infants with syndromic craniosynostosis: relationship with skull base and splanchnocranium sutural pattern.
    Calandrelli R, Pilato F, Massimi L, Panfili M, D'Apolito G, Gaudino S, Colosimo C.
    Neuroradiology; 2018 May 07; 60(5):517-528. PubMed ID: 29520643
    [Abstract] [Full Text] [Related]

  • 15. [Clinical and genetic characteristics of craniosynostosis].
    Bessenyei B, Oláh E.
    Orv Hetil; 2014 Mar 02; 155(9):341-7. PubMed ID: 24566698
    [Abstract] [Full Text] [Related]

  • 16. Are the acrocephalosyndactyly syndromes variable expressions of a single gene defect?
    Escobar V, Bixler D.
    Birth Defects Orig Artic Ser; 1977 Mar 02; 13(3C):139-54. PubMed ID: 890108
    [Abstract] [Full Text] [Related]

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  • 18. Mutation screening in patients with syndromic craniosynostoses indicates that a limited number of recurrent FGFR2 mutations accounts for severe forms of Pfeiffer syndrome.
    Lajeunie E, Heuertz S, El Ghouzzi V, Martinovic J, Renier D, Le Merrer M, Bonaventure J.
    Eur J Hum Genet; 2006 Mar 02; 14(3):289-98. PubMed ID: 16418739
    [Abstract] [Full Text] [Related]

  • 19. Facial skeleton dysmorphology in syndromic craniosynostosis: differences between FGFR2 and no-FGFR2-related syndromes and relationship with skull base and facial sutural patterns.
    Calandrelli R, Pilato F, Massimi L, D'Apolito G, Colosimo C.
    Childs Nerv Syst; 2023 Nov 02; 39(11):3235-3247. PubMed ID: 37195419
    [Abstract] [Full Text] [Related]

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