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Journal Abstract Search

254 related items for PubMed ID: 25633065

  • 1.
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  • 2. Imaging findings in congenital cranial dysinnervation disorders.
    Ferreira RM, Amaral LL, Gonçalves MV, Lin K.
    Top Magn Reson Imaging; 2011 Dec; 22(6):283-94. PubMed ID: 24132067
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  • 5. Congenital cranial dysinnervation disorders and more.
    Traboulsi EI.
    J AAPOS; 2007 Jun; 11(3):215-7. PubMed ID: 17572338
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  • 6. Congenital innervation dysgenesis syndrome (CID)/congenital cranial dysinnervation disorders (CCDDs).
    Assaf AA.
    Eye (Lond); 2011 Oct; 25(10):1251-61. PubMed ID: 21720410
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  • 9. A TUBB6 mutation is associated with autosomal dominant non-progressive congenital facial palsy, bilateral ptosis and velopharyngeal dysfunction.
    Fazeli W, Herkenrath P, Stiller B, Neugebauer A, Fricke J, Lang-Roth R, Nürnberg G, Thoenes M, Becker J, Altmüller J, Volk AE, Kubisch C, Heller R.
    Hum Mol Genet; 2017 Oct 15; 26(20):4055-4066. PubMed ID: 29016863
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  • 10. The ECEL1-related strabismus phenotype is consistent with congenital cranial dysinnervation disorder.
    Khan AO, Shaheen R, Alkuraya FS.
    J AAPOS; 2014 Aug 15; 18(4):362-7. PubMed ID: 25173900
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  • 11. [Advances in clinical and molecular genetics of congenital cranial dysinnervation disorders].
    Zhao J, Zhao KX, Tian YM.
    Zhonghua Yan Ke Za Zhi; 2007 Jan 15; 43(1):82-6. PubMed ID: 17442174
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  • 12. Bilateral incyclotorsion, absent facial nerve, and anotia: fellow travelers in Möbius sequence or oculoauriculovertebral spectrum?
    Pandey PK, Shroff D, Kapoor S, Kaur N, Srivastava N, Jain P, Garg D.
    J AAPOS; 2007 Jun 15; 11(3):310-2. PubMed ID: 17280850
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  • 15. Ocular congenital cranial dysinnervation disorders (CCDDs): insights into axon growth and guidance.
    Whitman MC, Engle EC.
    Hum Mol Genet; 2017 Aug 01; 26(R1):R37-R44. PubMed ID: 28459979
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  • 16. Magnetic resonance imaging of the endophenotype of a novel familial Möbius-like syndrome.
    Dumars S, Andrews C, Chan WM, Engle EC, Demer JL.
    J AAPOS; 2008 Aug 01; 12(4):381-9. PubMed ID: 18455936
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  • 18. Differentiating Moebius syndrome and other congenital facial weakness disorders with electrodiagnostic studies.
    Lehky T, Joseph R, Toro C, Wu T, Van Ryzin C, Gropman A, Facio FM, Webb BD, Jabs EW, Barry BS, Engle EC, Collins FS, Manoli I, Moebius Syndrome Research Consortium.
    Muscle Nerve; 2021 Apr 01; 63(4):516-524. PubMed ID: 33389762
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  • 19. Congenital Cranial Dysinnervation Disorders: A Literature Review.
    Fels R.
    Am Orthopt J; 2017 Jan 01; 67(1):89-92. PubMed ID: 28904220
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  • 20. CCDD Phenotype Associated with a Small Chromosome 2 Deletion.
    Abu-Amero KK, Bosley TM, Kondkar AA, Oystreck DT, Khan AO.
    Semin Ophthalmol; 2015 Jan 01; 30(5-6):435-42. PubMed ID: 24475916
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