135 related articles for article (PubMed ID: 10333105)
1. Wagner vitreoretinal degeneration with genetic linkage refinement on chromosome 5q13-q14.
Zech JC; Morlé L; Vincent P; Alloisio N; Bozon M; Gonnet C; Milazzo S; Grange JD; Trepsat C; Godet J; Plauchu H
Graefes Arch Clin Exp Ophthalmol; 1999 May; 237(5):387-93. PubMed ID: 10333105
[TBL] [Abstract][Full Text] [Related]
2. A novel hereditary developmental vitreoretinopathy with multiple ocular abnormalities localizing to a 5-cM region of chromosome 5q13-q14.
Black GC; Perveen R; Wiszniewski W; Dodd CL; Donnai D; McLeod D
Ophthalmology; 1999 Nov; 106(11):2074-81. PubMed ID: 10571340
[TBL] [Abstract][Full Text] [Related]
3. Snowflake vitreoretinal degeneration: follow-up of the original family.
Lee MM; Ritter R; Hirose T; Vu CD; Edwards AO
Ophthalmology; 2003 Dec; 110(12):2418-26. PubMed ID: 14644728
[TBL] [Abstract][Full Text] [Related]
4. Genetic linkage of snowflake vitreoretinal degeneration to chromosome 2q36.
Jiao X; Ritter R; Hejtmancik JF; Edwards AO
Invest Ophthalmol Vis Sci; 2004 Dec; 45(12):4498-503. PubMed ID: 15557460
[TBL] [Abstract][Full Text] [Related]
5. A frame shift mutation in a tissue-specific alternatively spliced exon of collagen 2A1 in Wagner's vitreoretinal degeneration.
Gupta SK; Leonard BC; Damji KF; Bulman DE
Am J Ophthalmol; 2002 Feb; 133(2):203-10. PubMed ID: 11812423
[TBL] [Abstract][Full Text] [Related]
6. Posterior chorioretinal atrophy and vitreous phenotype in a family with Stickler syndrome from a mutation in the COL2A1 gene.
Vu CD; Brown J; Körkkö J; Ritter R; Edwards AO
Ophthalmology; 2003 Jan; 110(1):70-7. PubMed ID: 12511349
[TBL] [Abstract][Full Text] [Related]
7. Wagner vitreoretinal degeneration. Follow-up of the original pedigree.
Graemiger RA; Niemeyer G; Schneeberger SA; Messmer EP
Ophthalmology; 1995 Dec; 102(12):1830-9. PubMed ID: 9098284
[TBL] [Abstract][Full Text] [Related]
8. Identification of a novel splice site mutation of the CSPG2 gene in a Japanese family with Wagner syndrome.
Miyamoto T; Inoue H; Sakamoto Y; Kudo E; Naito T; Mikawa T; Mikawa Y; Isashiki Y; Osabe D; Shinohara S; Shiota H; Itakura M
Invest Ophthalmol Vis Sci; 2005 Aug; 46(8):2726-35. PubMed ID: 16043844
[TBL] [Abstract][Full Text] [Related]
9. WAGNER syndrome: anatomic, functional and genetic characterization of a Portuguese family.
Araújo JR; Tavares-Ferreira J; Estrela-Silva S; Rocha P; Brandão E; Faria PA; Falcão-Reis F; Rocha-Sousa A
Graefes Arch Clin Exp Ophthalmol; 2018 Jan; 256(1):163-171. PubMed ID: 29071374
[TBL] [Abstract][Full Text] [Related]
10. Stickler syndrome and vitreoretinal degeneration: correlation between locus mutation and vitreous phenotype. Apropos of a case.
Parentin F; Sangalli A; Mottes M; Perissutti P
Graefes Arch Clin Exp Ophthalmol; 2001 Apr; 239(4):316-9. PubMed ID: 11450497
[TBL] [Abstract][Full Text] [Related]
11. Radial perivascular retinal degeneration: a key to the clinical diagnosis of an ocular variant of Stickler syndrome with minimal or no systemic manifestations.
Parma ES; Körkkö J; Hagler WS; Ala-Kokko L
Am J Ophthalmol; 2002 Nov; 134(5):728-34. PubMed ID: 12429250
[TBL] [Abstract][Full Text] [Related]
12. Clinical description and exclusion of candidate genes in a novel autosomal recessively inherited vitreoretinal dystrophy.
Sarra GM; Weigell-Weber M; Kotzot D; Niemeyer G; Messmer E; Hergersberg M
Arch Ophthalmol; 2003 Aug; 121(8):1109-16. PubMed ID: 12912687
[TBL] [Abstract][Full Text] [Related]
13. Identification of a stop codon mutation in exon 2 of the collagen 2A1 gene in a large stickler syndrome family.
Donoso LA; Edwards AO; Frost AT; Ritter R; Ahmad NN; Vrabec T; Rogers J; Meyer D
Am J Ophthalmol; 2002 Nov; 134(5):720-7. PubMed ID: 12429249
[TBL] [Abstract][Full Text] [Related]
14. Mutational hot spot potential of a novel base pair mutation of the CSPG2 gene in a family with Wagner syndrome.
Ronan SM; Tran-Viet KN; Burner EL; Metlapally R; Toth CA; Young TL
Arch Ophthalmol; 2009 Nov; 127(11):1511-9. PubMed ID: 19901218
[TBL] [Abstract][Full Text] [Related]
15. Erosive vitreoretinopathy. A new clinical entity.
Brown DM; Kimura AE; Weingeist TA; Stone EM
Ophthalmology; 1994 Apr; 101(4):694-704. PubMed ID: 8152765
[TBL] [Abstract][Full Text] [Related]
16. Wagner's hereditary vitreoretinal degeneration and retinal detachment.
Hirose T; Lee KY; Schepens CL
Arch Ophthalmol; 1973 Mar; 89(3):176-85. PubMed ID: 4691317
[No Abstract] [Full Text] [Related]
17. Clinical features of progressive bifocal chorioretinal atrophy: a retinal dystrophy linked to chromosome 6q.
Godley BF; Tiffin PA; Evans K; Kelsell RE; Hunt DM; Bird AC
Ophthalmology; 1996 Jun; 103(6):893-8. PubMed ID: 8643244
[TBL] [Abstract][Full Text] [Related]
18. Wagner's hereditary vitreoretinal degeneration.
Manning LM
Aust J Ophthalmol; 1980 Feb; 8(1):29-33. PubMed ID: 7387542
[TBL] [Abstract][Full Text] [Related]
19. Genetic linkage of Wagner disease and erosive vitreoretinopathy to chromosome 5q13-14.
Brown DM; Graemiger RA; Hergersberg M; Schinzel A; Messmer EP; Niemeyer G; Schneeberger SA; Streb LM; Taylor CM; Kimura AE
Arch Ophthalmol; 1995 May; 113(5):671-5. PubMed ID: 7748141
[TBL] [Abstract][Full Text] [Related]
20. Dominant late-onset retinal degeneration with regional variation of sub-retinal pigment epithelium deposits, retinal function, and photoreceptor degeneration.
Milam AH; Curcio CA; Cideciyan AV; Saxena S; John SK; Kruth HS; Malek G; Heckenlively JR; Weleber RG; Jacobson SG
Ophthalmology; 2000 Dec; 107(12):2256-66. PubMed ID: 11097607
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
