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Items: 1 to 20 of 115

1.

Coats-like retinopathy in an infant with preclinical facioscapulohumeral dystrophy.

Ganesh A, Kaliki S, Shields CL.

J AAPOS. 2012 Apr;16(2):204-6. doi: 10.1016/j.jaapos.2011.11.005.

PMID:
22525183
2.

Bilateral Coats' response in a female patient leads to diagnosis of facioscapulohumeral muscular dystrophy.

Bass SJ, Sherman J, Giovinazzo V.

Optometry. 2011 Feb;82(2):72-6. doi: 10.1016/j.optm.2010.07.028. Epub 2010 Dec 4.

PMID:
21130700
3.

Neovascular glaucoma from advanced Coats disease as the initial manifestation of facioscapulohumeral dystrophy in a 2-year-old child.

Shields CL, Zahler J, Falk N, Furuta M, Eagle RC Jr, Espinosa LE, Fischer PR, Shields JA.

Arch Ophthalmol. 2007 Jun;125(6):840-2. No abstract available.

PMID:
17563001
4.

Retinal telangiectasis detected during a vision screening examination in a child with hearing loss led to the diagnosis of facioscapulohumeral muscular dystrophy.

Lee GD, Chen VM, Barnes AC, Goldman DR, Duker JS.

J AAPOS. 2014 Jun;18(3):303-5. doi: 10.1016/j.jaapos.2014.02.009.

PMID:
24924285
5.

Detection of facial hypotonia and diagnosis of facioscapulohumeral dystrophy.

Sheth VS, Shapiro MJ.

Arch Ophthalmol. 2008 May;126(5):745-6; author reply 746. doi: 10.1001/archopht.126.5.745-c. No abstract available.

PMID:
18474804
6.

Subclinical facioscapulohumeral muscular dystrophy masquerading as bilateral Coats disease in a woman.

Vance SK, Wald KJ, Sherman J, Freund KB.

Arch Ophthalmol. 2011 Jun;129(6):807-9. doi: 10.1001/archophthalmol.2011.124. No abstract available.

PMID:
21670353
7.

[Literature review of the importance of retinal examination in two genetic neuromuscular diseases (DM1 and FSHD). Potential clinical applications].

Brignol TN.

J Fr Ophtalmol. 2015 Dec;38(10):e259-60. doi: 10.1016/j.jfo.2015.03.024. Epub 2015 Nov 5. Review. French. No abstract available.

PMID:
26547227
8.

Peripheral retinal nonperfusion in fellow eyes in coats disease.

Blair MP, Ulrich JN, Elizabeth Hartnett M, Shapiro MJ.

Retina. 2013 Sep;33(8):1694-9. doi: 10.1097/IAE.0b013e318285cb86.

PMID:
23974953
9.

Coats syndrome in facioscapulohumeral dystrophy type 1: frequency and D4Z4 contraction size.

Statland JM, Sacconi S, Farmakidis C, Donlin-Smith CM, Chung M, Tawil R.

Neurology. 2013 Mar 26;80(13):1247-50. doi: 10.1212/WNL.0b013e3182897116. Epub 2013 Feb 27.

10.

Reemergence of dormant Coats disease after 30 years.

Pérez-Campagne E, Wolfensberger TJ.

Eur J Ophthalmol. 2012 May-Jun;22(3):509-12. doi: 10.5301/ejo.5000040.

PMID:
21928259
11.

Full-thickness macular hole and macular telangiectasia in a child with Coats' disease.

Kumar V, Goel N, Ghosh B, Raina UK.

Ophthalmic Surg Lasers Imaging. 2010 Dec 30;41 Online:e1-3. doi: 10.3928/15428877-20101223-06.

PMID:
21210570
12.

Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy.

Osborne RJ, Welle S, Venance SL, Thornton CA, Tawil R.

Neurology. 2007 Feb 20;68(8):569-77. Epub 2006 Dec 6.

PMID:
17151338
13.

Vascular tortuosity and Coats'-like retinal changes in facioscapulohumeral muscular dystrophy.

Tekin NF, Saatci AO, Kavukçu S.

Ophthalmic Surg Lasers. 2000 Jan-Feb;31(1):82-3. No abstract available.

PMID:
10976570
14.

Spontaneous resolution of retinal vascular abnormalities and macular oedema in facioscapulohumeral muscular dystrophy.

Lindner M, Holz FG, Charbel Issa P.

Clin Exp Ophthalmol. 2016 Sep;44(7):627-628. doi: 10.1111/ceo.12735. Epub 2016 Apr 27. No abstract available.

PMID:
26933772
15.

Classification and management of Coats disease: the 2000 Proctor Lecture.

Shields JA, Shields CL, Honavar SG, Demirci H, Cater J.

Am J Ophthalmol. 2001 May;131(5):572-83.

PMID:
11336931
16.

Bilateral fluorescein angiographic findings in unilateral Coats' disease.

Shane TS, Berrocal AM, Hess DJ.

Ophthalmic Surg Lasers Imaging. 2011 Feb 10;42 Online:e15-7. doi: 10.3928/15428877-20110203-03.

PMID:
21323189
17.

Ocular findings and treatment of a young boy with Coats’ plus.

Yannuzzi NA, Tzu JH, Ko AC, Hess DJ, Cristian I, Berrocal AM.

Ophthalmic Surg Lasers Imaging Retina. 2014 Sep-Oct;45(5):462-5.

PMID:
25197929
18.

[Facioscapulohumeral muscular dystrophy. Clinical picture, atypical forms, diagnostics, genetics].

Jordan B, Müller-Reible C, Zierz S.

Nervenarzt. 2011 Jun;82(6):712-22. doi: 10.1007/s00115-010-2968-x. German.

PMID:
21567298
19.

Diagnostic challenges in facioscapulohumeral muscular dystrophy.

Sacconi S, Salviati L, Bourget I, Figarella D, Péréon Y, Lemmers R, van der Maarel S, Desnuelle C.

Neurology. 2006 Oct 24;67(8):1464-6.

PMID:
17060574
20.

Retinoschisis in the setting of Coats' disease.

Yannuzzi NA, Tzu JH, Hess DJ, Berrocal AM.

Ophthalmic Surg Lasers Imaging Retina. 2014 Mar-Apr;45(2):172-4. doi: 10.3928/23258160-20140306-13.

PMID:
24635161

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