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Items: 1 to 20 of 106

1.

Retinal arterial but not venous tortuosity correlates with facioscapulohumeral muscular dystrophy severity.

Longmuir SQ, Mathews KD, Longmuir RA, Joshi V, Olson RJ, Abràmoff MD.

J AAPOS. 2010 Jun;14(3):240-3. doi: 10.1016/j.jaapos.2010.03.006.

PMID:
20603058
2.

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
3.
4.

Muscle pathology grade for facioscapulohumeral muscular dystrophy biopsies.

Statland JM, Shah B, Henderson D, Van Der Maarel S, Tapscott SJ, Tawil R.

Muscle Nerve. 2015 Oct;52(4):521-6. doi: 10.1002/mus.24621. Epub 2015 Jun 18.

5.

Plus disease diagnosis in retinopathy of prematurity: vascular tortuosity as a function of distance from optic disk.

Keck KM, Kalpathy-Cramer J, Ataer-Cansizoglu E, You S, Erdogmus D, Chiang MF.

Retina. 2013 Sep;33(8):1700-7. doi: 10.1097/IAE.0b013e3182845c39.

6.

Expression of DUX4 in zebrafish development recapitulates facioscapulohumeral muscular dystrophy.

Mitsuhashi H, Mitsuhashi S, Lynn-Jones T, Kawahara G, Kunkel LM.

Hum Mol Genet. 2013 Feb 1;22(3):568-77. doi: 10.1093/hmg/dds467. Epub 2012 Oct 29.

7.

Retinal vessel tortuosity associated with central retinal vein occlusion: an optical coherence tomography study.

Muraoka Y, Tsujikawa A, Kumagai K, Akagi-Kurashige Y, Ogino K, Murakami T, Miyamoto K, Yoshimura N.

Invest Ophthalmol Vis Sci. 2014 Jan 7;55(1):134-41. doi: 10.1167/iovs.13-13201.

PMID:
24327610
8.

Low D4Z4 copy number and gender difference in Korean patients with facioscapulohumeral muscular dystrophy type 1.

Park HJ, Hong JM, Lee JH, Lee HS, Shin HY, Kim SM, Ki CS, Lee JH, Choi YC.

Neuromuscul Disord. 2015 Nov;25(11):859-64. doi: 10.1016/j.nmd.2015.08.004. Epub 2015 Aug 11.

PMID:
26319123
9.

FSHD-like patients without 4q35 deletion.

Yamanaka G, Goto K, Ishihara T, Oya Y, Miyajima T, Hoshika A, Nishino I, Hayashi YK.

J Neurol Sci. 2004 Apr 15;219(1-2):89-93.

PMID:
15050443
10.

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
11.

Diversity of retinal vascular anomalies in patients with familial exudative vitreoretinopathy.

Kashani AH, Brown KT, Chang E, Drenser KA, Capone A, Trese MT.

Ophthalmology. 2014 Nov;121(11):2220-7. doi: 10.1016/j.ophtha.2014.05.029. Epub 2014 Jul 5.

PMID:
25005911
12.

Oscillation of angiogenesis with vascular dropout in diabetic retinopathy by VESsel GENeration analysis (VESGEN).

Parsons-Wingerter P, Radhakrishnan K, Vickerman MB, Kaiser PK.

Invest Ophthalmol Vis Sci. 2010 Jan;51(1):498-507. doi: 10.1167/iovs.09-3968. Epub 2009 Sep 24.

13.

Facioscapulohumeral dystrophy with cochlear hearing loss and tortuosity of retinal vessels.

Gieron MA, Korthals JK, Kousseff BG.

Am J Med Genet. 1985 Sep;22(1):143-7.

PMID:
4050849
14.

Plus disease in retinopathy of prematurity: qualitative analysis of diagnostic process by experts.

Hewing NJ, Kaufman DR, Chan RV, Chiang MF.

JAMA Ophthalmol. 2013 Aug;131(8):1026-32. doi: 10.1001/jamaophthalmol.2013.135.

15.

The strength and functional performance in patients with facioscapulohumeral muscular dystrophy.

Lue YJ, Chen SS.

Kaohsiung J Med Sci. 2000 May;16(5):248-54.

PMID:
10969520
16.

Severe phenotype in infantile facioscapulohumeral muscular dystrophy.

Klinge L, Eagle M, Haggerty ID, Roberts CE, Straub V, Bushby KM.

Neuromuscul Disord. 2006 Oct;16(9-10):553-8. Epub 2006 Aug 24.

PMID:
16934468
17.

[Clinical and genetical features of Japanese early-onset facioscapulohumeral muscular dystrophy].

Yamanaka G, Goto K, Hayashi YK, Miyajima T, Hoshika A, Arahata K.

No To Hattatsu. 2002 Jul;34(4):318-24. Japanese.

PMID:
12134683
18.

Facioscapulohumeral muscular dystrophy.

Tawil R, Van Der Maarel SM.

Muscle Nerve. 2006 Jul;34(1):1-15. Review.

PMID:
16508966
19.

Retinal vessel diameters decrease with macular ganglion cell layer thickness in autosomal dominant optic atrophy and in healthy subjects.

Rönnbäck C, Grønskov K, Larsen M.

Acta Ophthalmol. 2014 Nov;92(7):670-4. doi: 10.1111/aos.12378. Epub 2014 Mar 11.

20.

Isolation and characterization of mesoangioblasts from facioscapulohumeral muscular dystrophy muscle biopsies.

Morosetti R, Mirabella M, Gliubizzi C, Broccolini A, Sancricca C, Pescatori M, Gidaro T, Tasca G, Frusciante R, Tonali PA, Cossu G, Ricci E.

Stem Cells. 2007 Dec;25(12):3173-82. Epub 2007 Aug 30.

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