189 related articles for article (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
[TBL] [Abstract][Full Text] [Related]
2. The ECEL1-related strabismus phenotype is consistent with congenital cranial dysinnervation disorder.
Khan AO; Shaheen R; Alkuraya FS
J AAPOS; 2014 Aug; 18(4):362-7. PubMed ID: 25173900
[TBL] [Abstract][Full Text] [Related]
3. Possible rare congenital dysinnervation disorder: congenital ptosis associated with adduction.
Mendes S; Beselga D; Campos S; Neves A; Campos J; Carvalho S; Silva E; Castro Sousa JP
Strabismus; 2015; 23(1):33-5. PubMed ID: 25581513
[TBL] [Abstract][Full Text] [Related]
4. CCDD Phenotype Associated with a Small Chromosome 2 Deletion.
Abu-Amero KK; Bosley TM; Kondkar AA; Oystreck DT; Khan AO
Semin Ophthalmol; 2015; 30(5-6):435-42. PubMed ID: 24475916
[TBL] [Abstract][Full Text] [Related]
5. Congenital cranial dysinnervation disorder in a boy with congenital mirror movements.
Al Shamrani M; Mahmoudi F; Abu-Amero KK; Khan AO
J AAPOS; 2015 Apr; 19(2):191-2. PubMed ID: 25838174
[TBL] [Abstract][Full Text] [Related]
6. Magnetic resonance imaging evidence for widespread orbital dysinnervation in dominant Duane's retraction syndrome linked to the DURS2 locus.
Demer JL; Clark RA; Lim KH; Engle EC
Invest Ophthalmol Vis Sci; 2007 Jan; 48(1):194-202. PubMed ID: 17197533
[TBL] [Abstract][Full Text] [Related]
7. Gustatory lid retraction: an unusual congenital cranial dysinnervation disorder.
Khan AO; Khan Z
J AAPOS; 2017 Dec; 21(6):511-512. PubMed ID: 29107795
[TBL] [Abstract][Full Text] [Related]
8. Congenital Cranial Dysinnervation Disorders: A Literature Review.
Fels R
Am Orthopt J; 2017 Jan; 67(1):89-92. PubMed ID: 28904220
[TBL] [Abstract][Full Text] [Related]
9. Congenital cranial dysinnervation disorders.
Singh A; Pandey PK; Agrawal A; Mittal SK; Rana KM; Bahuguna C
Int Ophthalmol; 2017 Dec; 37(6):1369-1381. PubMed ID: 27837354
[TBL] [Abstract][Full Text] [Related]
10. Ophthalmoplegia and Congenital Cranial Dysinnervation Disorders.
Oystreck DT
J Binocul Vis Ocul Motil; 2018; 68(1):31-33. PubMed ID: 30196776
[TBL] [Abstract][Full Text] [Related]
11. 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
[TBL] [Abstract][Full Text] [Related]
12. Considerations on the etiology of congenital Brown syndrome.
Coussens T; Ellis FJ
Curr Opin Ophthalmol; 2015 Jul; 26(5):357-61. PubMed ID: 26163776
[TBL] [Abstract][Full Text] [Related]
13. Strabismus surgery in congenital fibrosis of the extraocular muscles: a paradigm.
Sener EC; Taylan Sekeroglu H; Ural O; Oztürk BT; Sanaç AS
Ophthalmic Genet; 2014 Dec; 35(4):208-25. PubMed ID: 25347047
[TBL] [Abstract][Full Text] [Related]
14. Congenital cranial dysinnervation disorders: a concept in evolution.
Bosley TM; Abu-Amero KK; Oystreck DT
Curr Opin Ophthalmol; 2013 Sep; 24(5):398-406. PubMed ID: 23872818
[TBL] [Abstract][Full Text] [Related]
15. 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
[TBL] [Abstract][Full Text] [Related]
16. 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
[TBL] [Abstract][Full Text] [Related]
17. Alternating Hypotropia with Pseudoptosis: A New Phenotype of Congenital Cranial Dysinnervation Disorder.
Sedarous F; Chan TYB; Makar I
Case Rep Ophthalmol; 2018; 9(1):96-101. PubMed ID: 29643789
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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
[TBL] [Abstract][Full Text] [Related]
20. Ocular congenital cranial dysinnervation disorders (CCDDs): insights into axon growth and guidance.
Whitman MC; Engle EC
Hum Mol Genet; 2017 Aug; 26(R1):R37-R44. PubMed ID: 28459979
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]