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Journal Abstract Search

206 related items for PubMed ID: 8730180

  • 1. Skull base and calvarial deformities: association with intracranial changes in craniofacial syndromes.
    Tokumaru AM, Barkovich AJ, Ciricillo SF, Edwards MS.
    AJNR Am J Neuroradiol; 1996 Apr; 17(4):619-30. PubMed ID: 8730180
    [Abstract] [Full Text] [Related]

  • 2. Prominent basal emissary foramina in syndromic craniosynostosis: correlation with phenotypic and molecular diagnoses.
    Robson CD, Mulliken JB, Robertson RL, Proctor MR, Steinberger D, Barnes PD, McFarren A, Müller U, Zurakowski D.
    AJNR Am J Neuroradiol; 2000 Oct; 21(9):1707-17. PubMed ID: 11039354
    [Abstract] [Full Text] [Related]

  • 3. Does the association between abnormal anatomy of the skull base and cerebellar tonsillar position also exist in syndromic craniosynostosis?
    den Ottelander BK, Dremmen MHG, de Planque CA, van der Oest MJW, Mathijssen IMJ, van Veelen MC.
    J Plast Reconstr Aesthet Surg; 2022 Feb; 75(2):797-805. PubMed ID: 34799294
    [Abstract] [Full Text] [Related]

  • 4. Brain malformation in syndromic craniosynostoses, a primary disorder of white matter: a review.
    Raybaud C, Di Rocco C.
    Childs Nerv Syst; 2007 Dec; 23(12):1379-88. PubMed ID: 17882438
    [Abstract] [Full Text] [Related]

  • 5. Enigma of raised intracranial pressure in patients with complex craniosynostosis: the role of abnormal intracranial venous drainage.
    Taylor WJ, Hayward RD, Lasjaunias P, Britto JA, Thompson DN, Jones BM, Evans RD.
    J Neurosurg; 2001 Mar; 94(3):377-85. PubMed ID: 11235939
    [Abstract] [Full Text] [Related]

  • 6. Studies of malformation syndromes in man XXXVI: the Pfeiffer syndrome, association with Kleeblattschädel and multiple visceral anomalies. Case report and review.
    Hodach RJ, Viseskul C, Gilbert EF, Herrmann JP, Wolfson JJ, Kaveggia EG, Opitz JM.
    Z Kinderheilkd; 1975 Mar; 119(2):87-103. PubMed ID: 1136537
    [Abstract] [Full Text] [Related]

  • 7. Lack of association of cranial lacunae with intracranial hypertension in children with Crouzon syndrome and Apert syndrome: a 3D morphometric quantitative analysis.
    Mondal A, Rodriguez-Florez N, O'Hara J, Ong J, Jeelani NUO, Dunaway DJ, James G.
    Childs Nerv Syst; 2019 Mar; 35(3):501-507. PubMed ID: 30661112
    [Abstract] [Full Text] [Related]

  • 8. Q289P mutation in the FGFR2 gene: first report in a patient with type 1 Pfeiffer syndrome.
    Piccione M, Antona V, Niceta M, Fabiano C, Martines M, Bianchi A, Corsello G.
    Eur J Pediatr; 2009 Sep; 168(9):1135-9. PubMed ID: 19066959
    [Abstract] [Full Text] [Related]

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  • 10. Respective Roles of Craniosynostosis and Syndromic Influences on Cranial Fossa Development.
    Lu X, Forte AJ, Wilson AT, Park KE, Allam O, Alperovich M, Steinbacher DM, Alonso N, Persing JA.
    Plast Reconstr Surg; 2021 Jul 01; 148(1):145-156. PubMed ID: 34181610
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  • 12. Comparative three-dimensional analysis of CT-scans of the calvaria and cranial base in Apert and Crouzon syndromes.
    Kreiborg S, Marsh JL, Cohen MM, Liversage M, Pedersen H, Skovby F, Børgesen SE, Vannier MW.
    J Craniomaxillofac Surg; 1993 Jul 01; 21(5):181-8. PubMed ID: 8360349
    [Abstract] [Full Text] [Related]

  • 13. Reduced Intercarotid Artery Distance in Syndromic and Isolated Brachycephaly.
    Assadsangabi R, Hajmomenian M, Nabavizadeh SA, Schmitt JE, Vossough A.
    Pediatr Neurol; 2018 Feb 01; 79():3-7. PubMed ID: 29290519
    [Abstract] [Full Text] [Related]

  • 14. Palatal anomalies in the syndromes of Apert and Crouzon.
    Peterson SJ, Pruzansky S.
    Cleft Palate J; 1974 Oct 01; 11():394-403. PubMed ID: 4530751
    [No Abstract] [Full Text] [Related]

  • 15. Morphology of the foramen magnum in syndromic and non-syndromic brachycephaly.
    Assadsangabi R, Hajmomenian M, Bilaniuk LT, Vossough A.
    Childs Nerv Syst; 2015 May 01; 31(5):735-41. PubMed ID: 25686894
    [Abstract] [Full Text] [Related]

  • 16. Clinical features of syndromic craniosynostosis.
    Rice DP.
    Front Oral Biol; 2008 May 01; 12():91-106. PubMed ID: 18391497
    [Abstract] [Full Text] [Related]

  • 17. Syndromic Craniosynostosis.
    Wang JC, Nagy L, Demke JC.
    Facial Plast Surg Clin North Am; 2016 Nov 01; 24(4):531-543. PubMed ID: 27712819
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  • 19. Computed tomography assessment of Apert syndrome.
    Albuquerque MA, Cavalcanti MG.
    Braz Oral Res; 2004 Nov 01; 18(1):35-9. PubMed ID: 15273784
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