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Results: 1 to 20 of 241

1.

Late onset lattice corneal dystrophy with systemic familial amyloidosis, amyloidosis V, in an English family.

Stewart HS, Parveen R, Ridgway AE, Bonshek R, Black GC.

Br J Ophthalmol. 2000 Apr;84(4):390-4.

PMID:
10729296
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Survey of patients with granular, lattice, avellino, and Reis-Bücklers corneal dystrophies for mutations in the BIGH3 and gelsolin genes.

Afshari NA, Mullally JE, Afshari MA, Steinert RF, Adamis AP, Azar DT, Talamo JH, Dohlman CH, Dryja TP.

Arch Ophthalmol. 2001 Jan;119(1):16-22.

PMID:
11146721
[PubMed - indexed for MEDLINE]
3.

Lattice corneal dystrophy type II: clinical, pathologic, and molecular study in a Spanish family.

Huerva V, Velasco A, Sánchez MC, Mateo AJ, Matías-Guiu X.

Eur J Ophthalmol. 2007 May-Jun;17(3):424-9.

PMID:
17534828
[PubMed - indexed for MEDLINE]
4.

Danish type gelsolin related amyloidosis: 654G-T mutation is associated with a disease pathogenetically and clinically similar to that caused by the 654G-A mutation (familial amyloidosis of the Finnish type).

Maury CP, Liljeström M, Boysen G, Törnroth T, de la Chapelle A, Nurmiaho-Lassila EL.

J Clin Pathol. 2000 Feb;53(2):95-9.

PMID:
10767822
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Exclusion of the gelsolin gene on 9q32-34 as the cause of familial lattice corneal dystrophy type I.

Wiens A, Marles S, Safneck J, Kwiatkowski DJ, Maury CP, Zelinski T, Philipps S, Ekins MB, Greenberg CR.

Am J Hum Genet. 1992 Jul;51(1):156-60.

PMID:
1319113
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Two mutations in the TGFBI (BIGH3) gene associated with lattice corneal dystrophy in an extensively studied family.

Klintworth GK, Bao W, Afshari NA.

Invest Ophthalmol Vis Sci. 2004 May;45(5):1382-8.

PMID:
15111592
[PubMed - indexed for MEDLINE]
Free Article
7.

Heavy-chain amyloidosis in TGFBI-negative and gelsolin-negative atypical lattice corneal dystrophy.

Pradhan MA, Henderson RA, Patel D, McGhee CN, Vincent AL.

Cornea. 2011 Oct;30(10):1163-6. doi: 10.1097/ICO.0b013e31821142b5.

PMID:
21743312
[PubMed - indexed for MEDLINE]
8.

TGFBI (BIGH3) gene mutations in Hungary--report of the novel F547S mutation associated with polymorphic corneal amyloidosis.

Takács L, Losonczy G, Matesz K, Balogh I, Sohajda Z, Tóth K, Fazakas F, Vereb G, Berta A.

Mol Vis. 2007 Oct 18;13:1976-83.

PMID:
17982422
[PubMed - indexed for MEDLINE]
Free Article
9.

Lattice corneal dystrophy type IIIA. Clinical and histopathologic correlations.

Stock EL, Feder RS, O'Grady RB, Sugar J, Roth SI.

Arch Ophthalmol. 1991 Mar;109(3):354-8.

PMID:
2003794
[PubMed - indexed for MEDLINE]
10.

Meretoja syndrome. Lattice dystrophy of the cornea with hereditary generalized amyloidosis.

Donders PC, Blanksma LJ.

Ophthalmologica. 1979;178(3):173-80.

PMID:
314081
[PubMed - indexed for MEDLINE]
11.

Late-onset form of lattice corneal dystrophy caused by leu527Arg mutation of the TGFBI gene.

Hirano K, Hotta Y, Nakamura M, Fujiki K, Kanai A, Yamamoto N.

Cornea. 2001 Jul;20(5):525-9.

PMID:
11413411
[PubMed - indexed for MEDLINE]
12.

Danish type gelsolin-related amyloidosis in a Brazilian family: case reports.

Solari HP, Ventura MP, Antecka E, Belfort Junior R, Burnier MN Jr.

Arq Bras Oftalmol. 2011 Jul-Aug;74(4):286-8.

PMID:
22068858
[PubMed - indexed for MEDLINE]
Free Article
13.

Corneal morphology and sensitivity in lattice dystrophy type II (familial amyloidosis, Finnish type).

Rosenberg ME, Tervo TM, Gallar J, Acosta MC, Müller LJ, Moilanen JA, Tarkkanen AH, Vesaluoma MH.

Invest Ophthalmol Vis Sci. 2001 Mar;42(3):634-41.

PMID:
11222521
[PubMed - indexed for MEDLINE]
Free Article
14.

Anticipation in familial lattice corneal dystrophy type I with R124C mutation in the TGFBI (BIGH3) gene.

Romero P, Vogel M, Diaz JM, Romero MP, Herrera L.

Mol Vis. 2008 May 7;14:829-35.

PMID:
18470323
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

[Molecular genetic analysis of the BIGH3 gene in lattice type I (Biber-Haab-Dimmer) and granular type II (Avellino) corneal dystrophy: is indirect mutation analysis for hot spots recommended?].

Grünauer-Kloevekorn C, Bräutigam S, Wolter-Roessler M, Tost F, Weidle E, Froster U, Duncker GI.

Klin Monbl Augenheilkd. 2005 Dec;222(12):1017-23. German.

PMID:
16380889
[PubMed - indexed for MEDLINE]
16.

[Hereditary gelsolin amyloidosis--40 years of Meretoja disease].

Kiuru-Enari S, Haltia M.

Duodecim. 2010;126(10):1162-71. Review. Finnish.

PMID:
20597346
[PubMed - indexed for MEDLINE]
17.

[Familial amyloidosis, Finnish type with marked anhidrosis].

Ishiguchi H, Shimoya K, Ohnishi A, Murai Y, Nakazato M, Hoshii Y.

Rinsho Shinkeigaku. 1996 Mar;36(3):436-41. Japanese.

PMID:
8741346
[PubMed - indexed for MEDLINE]
18.

Lattice corneal dystrophy type II associated with familial amyloid polyneuropathy type IV.

Akiya S, Nishio Y, Ibi K, Uozumi H, Takahashi H, Hamada T, Onishi A, Ishiguchi H, Hoshii Y, Nakazato M.

Ophthalmology. 1996 Jul;103(7):1106-10.

PMID:
8684801
[PubMed - indexed for MEDLINE]
19.

Clinical and histopathologic studies of two families with lattice corneal dystrophy and familial systemic amyloidosis (Meretoja syndrome).

Starck T, Kenyon KR, Hanninen LA, Beyer-Machule C, Fabian R, Gorn RA, McMullan FD, Baum J, McAdam KP.

Ophthalmology. 1991 Aug;98(8):1197-206.

PMID:
1923356
[PubMed - indexed for MEDLINE]
20.

A clinical, histopathological, and genetic study of Avellino corneal dystrophy in British families.

El-Ashry MF, Abd El-Aziz MM, Larkin DF, Clarke B, Cree IA, Hardcastle AJ, Bhattacharya SS, Ebenezer ND.

Br J Ophthalmol. 2003 Jul;87(7):839-42.

PMID:
12812879
[PubMed - indexed for MEDLINE]
Free PMC Article

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