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Results: 1 to 20 of 119

1.

Best vitelliform macular dystrophy in a Swedish family: genetic analysis and a seven-year follow-up of photodynamic treatment of a young boy with choroidal neovascularization.

Frennesson CI, Wadelius C, Nilsson SE.

Acta Ophthalmol. 2014 May;92(3):238-42. doi: 10.1111/aos.12142. Epub 2013 Apr 26.

PMID:
23617333
[PubMed - indexed for MEDLINE]
2.

Autosomal recessive best vitelliform macular dystrophy: report of a family and management of early-onset neovascular complications.

Iannaccone A, Kerr NC, Kinnick TR, Calzada JI, Stone EM.

Arch Ophthalmol. 2011 Feb;129(2):211-7. doi: 10.1001/archophthalmol.2010.367.

PMID:
21320969
[PubMed - indexed for MEDLINE]
3.

Functional and clinical data of Best vitelliform macular dystrophy patients with mutations in the BEST1 gene.

Querques G, Zerbib J, Santacroce R, Margaglione M, Delphin N, Rozet JM, Kaplan J, Martinelli D, Delle Noci N, Soubrane G, Souied EH.

Mol Vis. 2009 Dec 31;15:2960-72.

PMID:
20057903
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Phenotypic variability in a French family with a novel mutation in the BEST1 gene causing multifocal best vitelliform macular dystrophy.

Lacassagne E, Dhuez A, Rigaudière F, Dansault A, Vêtu C, Bigot K, Vieira V, Puech B, Defoort-Dhellemmes S, Abitbol M.

Mol Vis. 2011 Jan 29;17:309-22.

PMID:
21293734
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Photodynamic therapy for best disease complicated by choroidal neovascularization in children.

Ozdek S, Ozmen MC, Tufan HA, Gurelik G, Hasanreisoglu B.

J Pediatr Ophthalmol Strabismus. 2012 Jul-Aug;49(4):216-21. doi: 10.3928/01913913-20111004-01. Epub 2011 Oct 11.

PMID:
21985152
[PubMed - indexed for MEDLINE]
6.

Intravitreal bevacizumab for choroidal neovascularization secondary to Best vitelliform macular dystrophy in a 6-year-old child.

Chhablani J, Jalali S.

Eur J Ophthalmol. 2012 Jul-Aug;22(4):677-9. doi: 10.5301/ejo.5000095.

PMID:
22139615
[PubMed - indexed for MEDLINE]
7.

Best's vitelliform macular dystrophy caused by a new mutation (Val89Ala) in the VMD2 gene.

Eksandh L, Bakall B, Bauer B, Wadelius C, Andréasson S.

Ophthalmic Genet. 2001 Jun;22(2):107-15.

PMID:
11449320
[PubMed - indexed for MEDLINE]
9.

Frequency, genotype, and clinical spectrum of best vitelliform macular dystrophy: data from a national center in Denmark.

Bitner H, Schatz P, Mizrahi-Meissonnier L, Sharon D, Rosenberg T.

Am J Ophthalmol. 2012 Aug;154(2):403-412.e4. doi: 10.1016/j.ajo.2012.02.036. Epub 2012 May 24.

PMID:
22633354
[PubMed - indexed for MEDLINE]
11.

The spectrum of subclinical Best vitelliform macular dystrophy in subjects with mutations in BEST1 gene.

Querques G, Zerbib J, Santacroce R, Margaglione M, Delphin N, Querques L, Rozet JM, Kaplan J, Souied EH.

Invest Ophthalmol Vis Sci. 2011 Jun 28;52(7):4678-84. doi: 10.1167/iovs.10-6500.

PMID:
21436265
[PubMed - indexed for MEDLINE]
Free Article
12.

Ranibizumab for choroidal neovascularization associated with adult-onset foveomacular vitelliform dystrophy: one-year results.

Mimoun G, Caillaux V, Querques G, Rothschild PR, Puche N, Souied EH.

Retina. 2013 Mar;33(3):513-21. doi: 10.1097/IAE.0b013e3182753adb.

PMID:
23400081
[PubMed - indexed for MEDLINE]
13.

Preferential hyperacuity perimeter in best vitelliform macular dystrophy.

Querques G, Atmani K, Bouzitou-Mfoumou R, Leveziel N, Massamba N, Souied EH.

Retina. 2011 May;31(5):959-66. doi: 10.1097/IAE.0b013e3181f441c1.

PMID:
21242858
[PubMed - indexed for MEDLINE]
14.

A homozygous frameshift mutation in BEST1 causes the classical form of Best disease in an autosomal recessive mode.

Bitner H, Mizrahi-Meissonnier L, Griefner G, Erdinest I, Sharon D, Banin E.

Invest Ophthalmol Vis Sci. 2011 Jul 18;52(8):5332-8. doi: 10.1167/iovs.11-7174.

PMID:
21467170
[PubMed - indexed for MEDLINE]
Free Article
15.

Autosomal dominant Best disease with an unusual electrooculographic light rise and risk of angle-closure glaucoma: a clinical and molecular genetic study.

Low S, Davidson AE, Holder GE, Hogg CR, Bhattacharya SS, Black GC, Foster PJ, Webster AR.

Mol Vis. 2011;17:2272-82. Epub 2011 Aug 23.

PMID:
21921978
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Evaluation of macular structure and function by OCT and electrophysiology in patients with vitelliform macular dystrophy due to mutations in BEST1.

Schatz P, Bitner H, Sander B, Holfort S, Andreasson S, Larsen M, Sharon D.

Invest Ophthalmol Vis Sci. 2010 Sep;51(9):4754-65. doi: 10.1167/iovs.10-5152. Epub 2010 Apr 7.

PMID:
20375334
[PubMed - indexed for MEDLINE]
Free Article
17.

Anterior segment abnormalities and angle-closure glaucoma in a family with a mutation in the BEST1 gene and Best vitelliform macular dystrophy.

Wittström E, Ponjavic V, Bondeson ML, Andréasson S.

Ophthalmic Genet. 2011 Nov;32(4):217-27. doi: 10.3109/13816810.2011.567884. Epub 2011 Apr 7.

PMID:
21473666
[PubMed - indexed for MEDLINE]
18.

Identification of a novel VMD2 mutation in Japanese patients with Best disease.

Yanagi Y, Sekine H, Mori M.

Ophthalmic Genet. 2002 Jun;23(2):129-33.

PMID:
12187431
[PubMed - indexed for MEDLINE]
19.

[Intravitreal bevacizumab treatment for choroidal neovascularization in Best's disease].

Perol J, Wolff B, Sahel JA, Le Mer Y.

J Fr Ophtalmol. 2011 May;34(5):281-6. doi: 10.1016/j.jfo.2010.11.021. Epub 2011 Apr 20. French.

PMID:
21507509
[PubMed - indexed for MEDLINE]
Free Article
20.

Photodynamic therapy with verteporfin for subfoveal choroidal neovascularization in best disease.

Andrade RE, Farah ME, Costa RA.

Am J Ophthalmol. 2003 Dec;136(6):1179-81.

PMID:
14644242
[PubMed - indexed for MEDLINE]

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