202 related articles for article (PubMed ID: 25803556)
21. The molecular basis of the congenital fibrosis syndromes.
Engle EC
Strabismus; 2002 Jun; 10(2):125-8. PubMed ID: 12221491
[TBL] [Abstract][Full Text] [Related]
22. Congenital fibrosis of extraocular muscle type 1A due to KIF21A mutation: first case report from Hong Kong.
Luk HM; Lo IF; Lai CW; Ma LC; Tong TM; Chan DH; Lam ST
Hong Kong Med J; 2013 Apr; 19(2):182-5. PubMed ID: 23535681
[TBL] [Abstract][Full Text] [Related]
23. [Advances in clinical and molecular genetics of congenital cranial dysinnervation disorders].
Zhao J; Zhao KX; Tian YM
Zhonghua Yan Ke Za Zhi; 2007 Jan; 43(1):82-6. PubMed ID: 17442174
[TBL] [Abstract][Full Text] [Related]
24. [Inherited ophthalmological disorders. Part 2: Diagnostics and therapeutic concepts].
Preising MN; Stieger K; Lorenz B
Klin Monbl Augenheilkd; 2014 Feb; 231(2):e1-15; quiz e16-7. PubMed ID: 24532408
[No Abstract] [Full Text] [Related]
25. Imaging of Cranial Nerves III, IV, VI in Congenital Cranial Dysinnervation Disorders.
Kim JH; Hwang JM
Korean J Ophthalmol; 2017 Jun; 31(3):183-193. PubMed ID: 28534340
[TBL] [Abstract][Full Text] [Related]
26. Congenital fibrosis of the extraocular muscles.
Heidary G; Engle EC; Hunter DG
Semin Ophthalmol; 2008; 23(1):3-8. PubMed ID: 18214786
[TBL] [Abstract][Full Text] [Related]
27. Imaging of congenital cranial dysinnervation disorders: What radiologist wants to know?
Razek AAKA; Maher H; Kasem MA; Helmy E
Clin Imaging; 2021 Mar; 71():106-116. PubMed ID: 33189029
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. Absence of the trochlear nerve in patients with superior oblique hypoplasia.
Kim JH; Hwang JM
Ophthalmology; 2010 Nov; 117(11):2208-13.e1-2. PubMed ID: 20570358
[TBL] [Abstract][Full Text] [Related]
30. Hereditary external ophthalmoplegia synergistic divergence, jaw winking, and oculocutaneous hypopigmentation: a congenital fibrosis syndrome caused by deficient innervation to extraocular muscles.
Brodsky MC
Ophthalmology; 1998 Apr; 105(4):717-25. PubMed ID: 9544647
[TBL] [Abstract][Full Text] [Related]
31. Retinal Dysfunction in Patients with Congenital Fibrosis of the Extraocular Muscles Type 2.
Khan AO; Almutlaq M; Oystreck DT; Engle EC; Abu-Amero K; Bosley T
Ophthalmic Genet; 2016 Jun; 37(2):130-6. PubMed ID: 24940936
[TBL] [Abstract][Full Text] [Related]
32. [A family of congenital fibrosis of extraocular muscles associated with juvenile canities].
Zhao J; Zhao KX; Li ND; Jiao YH; Yang YJ; Tian YM
Zhonghua Yan Ke Za Zhi; 2007 Apr; 43(4):319-23. PubMed ID: 17605927
[TBL] [Abstract][Full Text] [Related]
33. [A family of congenital fibrosis of extraocular muscles associated with naso-sinusitis].
Zhou LH; Wu L; Zhu Y; Wang J; Xing YQ
Zhonghua Yan Ke Za Zhi; 2012 Mar; 48(3):262-6. PubMed ID: 22800426
[TBL] [Abstract][Full Text] [Related]
34. KIF21A pathogenic variants cause congenital fibrosis of extraocular muscles type 3.
Al-Haddad C; Boustany RM; Rachid E; Ismail K; Barry B; Chan WM; Engle E
Ophthalmic Genet; 2021 Apr; 42(2):195-199. PubMed ID: 33251926
[No Abstract] [Full Text] [Related]
35. Congenital fibrosis of the extra-ocular muscles (CFEOM) and the cranial dysinnervation disorders.
Vivian AJ
Eye (Lond); 2020 Feb; 34(2):251-255. PubMed ID: 31804624
[TBL] [Abstract][Full Text] [Related]
36. 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; 26(20):4055-4066. PubMed ID: 29016863
[TBL] [Abstract][Full Text] [Related]
37. Synergistic convergence and split pons in horizontal gaze palsy and progressive scoliosis in two sisters.
Jain NR; Jethani J; Narendran K; Kanth L
Indian J Ophthalmol; 2011; 59(2):162-5. PubMed ID: 21350292
[TBL] [Abstract][Full Text] [Related]
38. Congenital fibrosis of the extraocular muscles type 2, an inherited exotropic strabismus fixus, maps to distal 11q13.
Wang SM; Zwaan J; Mullaney PB; Jabak MH; Al-Awad A; Beggs AH; Engle EC
Am J Hum Genet; 1998 Aug; 63(2):517-25. PubMed ID: 9683611
[TBL] [Abstract][Full Text] [Related]
39. 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. PubMed ID: 24612975
[TBL] [Abstract][Full Text] [Related]
40. Congenital fibrosis of the extraocular muscles: review of recent literature.
Price JM; Boparai RS; Wasserman BN
Curr Opin Ophthalmol; 2019 Sep; 30(5):314-318. PubMed ID: 31313749
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
