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Journal Abstract Search
189 related items for PubMed ID: 18930669
1. A novel form of aberrant innervation in congenital cranial dysinnervation disorder. Khan AO. J AAPOS; 2009 Feb; 13(1):105-6. PubMed ID: 18930669 [Abstract] [Full Text] [Related]
12. Evidence of an asymmetrical endophenotype in congenital fibrosis of extraocular muscles type 3 resulting from TUBB3 mutations. Demer JL, Clark RA, Tischfield MA, Engle EC. Invest Ophthalmol Vis Sci; 2010 Sep; 51(9):4600-11. PubMed ID: 20393110 [Abstract] [Full Text] [Related]
16. 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 [Abstract] [Full Text] [Related]
17. Splitting of the extraocular horizontal rectus muscle in congenital cranial dysinnervation disorders. Okanobu H, Kono R, Miyake K, Ohtsuki H. Am J Ophthalmol; 2009 Mar; 147(3):550-556.e1. PubMed ID: 19038376 [Abstract] [Full Text] [Related]
18. Alternating Hypotropia with Pseudoptosis: A New Phenotype of Congenital Cranial Dysinnervation Disorder. Sedarous F, Chan TYB, Makar I. Case Rep Ophthalmol; 2018 Mar; 9(1):96-101. PubMed ID: 29643789 [Abstract] [Full Text] [Related]
19. Large-angle congenital exotropia due to 'absent' medial recti: a case of congenital cranial dysinnervation disorder. Houtman AC, Hocking G, Lloyd C, Biswas S. Eye (Lond); 2009 Jun; 23(6):1489-90. PubMed ID: 18600250 [No Abstract] [Full Text] [Related]
20. Magnetic resonance imaging evidence for widespread orbital dysinnervation in congenital fibrosis of extraocular muscles due to mutations in KIF21A. Demer JL, Clark RA, Engle EC. Invest Ophthalmol Vis Sci; 2005 Feb; 46(2):530-9. PubMed ID: 15671279 [Abstract] [Full Text] [Related] Page: [Next] [New Search]