Piguet B - Search Results

1

Linkage of autosomal dominant radial drusen (malattia leventinese) to chromosome 2p16-21.

Héon E, Piguet B, Munier F, Sneed SR, Morgan CM, Forni S, Pescia G, Schorderet D, Taylor CM, Streb LM, Wiles CD, Nishimura DY, Sheffield VC, Stone EM. Héon E, et al. Among authors: piguet b. Arch Ophthalmol. 1996 Feb;114(2):193-8. doi: 10.1001/archopht.1996.01100130187014. Arch Ophthalmol. 1996. PMID: 8573024

2

Full characterization of the maculopathy associated with an Arg-172-Trp mutation in the RDS/peripherin gene.

Piguet B, Héon E, Munier FL, Grounauer PA, Niemeyer G, Butler N, Schorderet DF, Sheffield VC, Stone EM. Piguet B, et al. Ophthalmic Genet. 1996 Dec;17(4):175-86. doi: 10.3109/13816819609057891. Ophthalmic Genet. 1996. PMID: 9010868

3

A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy.

Stone EM, Lotery AJ, Munier FL, Héon E, Piguet B, Guymer RH, Vandenburgh K, Cousin P, Nishimura D, Swiderski RE, Silvestri G, Mackey DA, Hageman GS, Bird AC, Sheffield VC, Schorderet DF. Stone EM, et al. Among authors: piguet b. Nat Genet. 1999 Jun;22(2):199-202. doi: 10.1038/9722. Nat Genet. 1999. PMID: 10369267

4

[Mutational screening of peripherin/RDS genes, rhodopsin and ROM-1 in 69 index cases with retinitis pigmentosa and other retinal dystrophies].

Millá E, Héon E, Piguet B, Ducrey N, Butler N, Stone E, Schorderet DF, Munier F. Millá E, et al. Among authors: piguet b. Klin Monbl Augenheilkd. 1998 May;212(5):305-8. Klin Monbl Augenheilkd. 1998. PMID: 9677563 French.

5

Rhodopsin C110Y mutation causes a type 2 autosomal dominant retinitis pigmentosa.

Millá E, Héon E, Grounauer PA, Piguet B, Ducrey N, Stone EM, Schorderet DF, Munier FL. Millá E, et al. Among authors: piguet b. Ophthalmic Genet. 1998 Sep;19(3):131-9. doi: 10.1076/opge.19.3.131.2183. Ophthalmic Genet. 1998. PMID: 9810568

6

A preliminary study of photodynamic therapy using verteporfin for choroidal neovascularization in pathologic myopia, ocular histoplasmosis syndrome, angioid streaks, and idiopathic causes.

Sickenberg M, Schmidt-Erfurth U, Miller JW, Pournaras CJ, Zografos L, Piguet B, Donati G, Laqua H, Barbazetto I, Gragoudas ES, Lane AM, Birngruber R, van den Bergh H, Strong HA, Manjuris U, Gray T, Fsadni M, Bressler NM. Sickenberg M, et al. Among authors: piguet b. Arch Ophthalmol. 2000 Mar;118(3):327-36. doi: 10.1001/archopht.118.3.327. Arch Ophthalmol. 2000. PMID: 10721954 Clinical Trial.

7

Chorioretinal vascular abnormalities associated with angioid streaks and pseudoxanthoma elasticum.

Secrétan M, Zografos L, Guggisberg D, Piguet B. Secrétan M, et al. Among authors: piguet b. Arch Ophthalmol. 1998 Oct;116(10):1333-6. doi: 10.1001/archopht.116.10.1333. Arch Ophthalmol. 1998. PMID: 9790632

8

Age-related macular disease in rural southern Italy.

Pagliarini S, Moramarco A, Wormald RP, Piguet B, Carresi C, Balacco-Gabrieli C, Sehmi KS, Bird AC. Pagliarini S, et al. Among authors: piguet b. Arch Ophthalmol. 1997 May;115(5):616-22. doi: 10.1001/archopht.1997.01100150618007. Arch Ophthalmol. 1997. PMID: 9152129

9

[Pattern dystrophies and intrafamilial phenotypic variation].

Bernasconi OR, Piguet B. Bernasconi OR, et al. Among authors: piguet b. Klin Monbl Augenheilkd. 1996 May;208(5):291-3. doi: 10.1055/s-2008-1035218. Klin Monbl Augenheilkd. 1996. PMID: 8766030 French.

10

Indocyanine green angiographic features in tuberculous chorioretinitis.

Wolfensberger TJ, Piguet B, Herbort CP. Wolfensberger TJ, et al. Among authors: piguet b. Am J Ophthalmol. 1999 Mar;127(3):350-3. doi: 10.1016/s0002-9394(98)00325-0. Am J Ophthalmol. 1999. PMID: 10088753

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