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Items: 20


Training in Compensatory Strategies Enhances Rapport in Interactions Involving People with Möbius Syndrome.

Michael J, Bogart K, Tylén K, Krueger J, Bech M, Østergaard JR, Fusaroli R.

Front Neurol. 2015 Oct 8;6:213. doi: 10.3389/fneur.2015.00213. eCollection 2015.


Congenital Corneal Anesthesia and Neurotrophic Keratitis: Diagnosis and Management.

Mantelli F, Nardella C, Tiberi E, Sacchetti M, Bruscolini A, Lambiase A.

Biomed Res Int. 2015;2015:805876. doi: 10.1155/2015/805876. Epub 2015 Sep 16. Review.


Cranial nerve development requires co-ordinated Shh and canonical Wnt signaling.

Kurosaka H, Trainor PA, Leroux-Berger M, Iulianella A.

PLoS One. 2015 Mar 23;10(3):e0120821. doi: 10.1371/journal.pone.0120821. eCollection 2015.


A novel de novo KIF21A mutation in a patient with congenital fibrosis of the extraocular muscles and Möbius syndrome.

Ali Z, Xing C, Anwar D, Itani K, Weakley D, Gong X, Pascual JM, Mootha VV.

Mol Vis. 2014 Mar 28;20:368-75. eCollection 2014.


Diagnostic distinctions and genetic analysis of patients diagnosed with moebius syndrome.

MacKinnon S, Oystreck DT, Andrews C, Chan WM, Hunter DG, Engle EC.

Ophthalmology. 2014 Jul;121(7):1461-8. doi: 10.1016/j.ophtha.2014.01.006. Epub 2014 Mar 6.


Characterization of ocular motor deficits in congenital facial weakness: Moebius and related syndromes.

Rucker JC, Webb BD, Frempong T, Gaspar H, Naidich TP, Jabs EW.

Brain. 2014 Apr;137(Pt 4):1068-79. doi: 10.1093/brain/awu021. Epub 2014 Feb 21.


First report of generalized face processing difficulties in möbius sequence.

Bate S, Cook SJ, Mole J, Cole J.

PLoS One. 2013 Apr 24;8(4):e62656. doi: 10.1371/journal.pone.0062656. Print 2013.


A boy with homozygous microdeletion of NEUROG1 presents with a congenital cranial dysinnervation disorder [Moebius syndrome variant].

Schröder JC, Läßig AK, Galetzka D, Peters A, Castle JC, Diederich S, Zechner U, Müller-Forell W, Keilmann A, Bartsch O.

Behav Brain Funct. 2013 Feb 18;9:7. doi: 10.1186/1744-9081-9-7.


HOXB1 founder mutation in humans recapitulates the phenotype of Hoxb1-/- mice.

Webb BD, Shaaban S, Gaspar H, Cunha LF, Schubert CR, Hao K, Robson CD, Chan WM, Andrews C, MacKinnon S, Oystreck DT, Hunter DG, Iacovelli AJ, Ye X, Camminady A, Engle EC, Jabs EW.

Am J Hum Genet. 2012 Jul 13;91(1):171-9. doi: 10.1016/j.ajhg.2012.05.018. Epub 2012 Jul 5.


Maternal homocystinuria and Moebius syndrome? Vascular aetiology.

Gupta N, Anthony MY.

BMJ Case Rep. 2011 Feb 14;2011. pii: bcr0920103331. doi: 10.1136/bcr.09.2010.3331.


Poland sequence: Series of two cases and brief review of the literature.

Garg R, Saheer S, Gupta V, Mehra S.

Ann Thorac Med. 2012 Apr;7(2):110-2. doi: 10.4103/1817-1737.94535.


Congenital innervation dysgenesis syndrome (CID)/congenital cranial dysinnervation disorders (CCDDs).

Assaf AA.

Eye (Lond). 2011 Oct;25(10):1251-61. doi: 10.1038/eye.2011.38. Epub 2011 Jul 1. Review.


HOXA1 mutations are not a common cause of Möbius syndrome.

Rankin JK, Andrews C, Chan WM, Engle EC.

J AAPOS. 2010 Feb;14(1):78-80. doi: 10.1016/j.jaapos.2009.11.007.


Occipito-vertebral dissociation in connection with extensive cervical spine malsegmentation in a boy with Möbius syndrome.

Al Kaissi A, Klaushofer K, Grill F.

Clinics (Sao Paulo). 2009;64(10):1034-6. doi: 10.1590/S1807-59322009001000016. No abstract available.


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;12(4):381-9. doi: 10.1016/j.jaapos.2008.01.018. Epub 2008 May 2.


Möbius syndrome in association with the REM sleep behaviour disorder.

Anderson K, Shneerson J, Smith I.

J Neurol Neurosurg Psychiatry. 2007 Jun;78(6):659-60. No abstract available.


Moebius-Poland syndrome and hypogonadotropic hypogonadism.

López de Lara D, Cruz-Rojo J, Sánchez del Pozo J, Gallego Gómez ME, Lledó Valera G.

Eur J Pediatr. 2008 Mar;167(3):353-4. Epub 2007 Mar 31. No abstract available.


HOXA1 mutations are not a common cause of Duane anomaly.

Tischfield MA, Chan WM, Grunert JF, Andrews C, Engle EC.

Am J Med Genet A. 2006 Apr 15;140(8):900-2. Review. No abstract available.

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