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Showing results (41-50 of 52) with videos related to

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Eye (London, England)|March 27, 2002
Symptomatic abnormalities of dark adaptation in patients with EFEMP1 retinal dystrophy (Malattia Leventinese/Doyne honeycomb retinal dystrophy)R Haimovici, J Wroblewski, B Piguet, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|May 1, 1997
Age-related macular disease in rural southern ItalyS Pagliarini, A Moramarco, R P Wormald, et al.
Ophthalmic Genetics|November 12, 1998
Rhodopsin C110Y mutation causes a type 2 autosomal dominant retinitis pigmentosaE Millá, E Héon, P A Grounauer, et al.
Ophthalmology|September 1, 1994
Bilateral macular drusen in age-related macular degeneration. Prognosis and risk factorsF G Holz, T J Wolfensberger, B Piguet, et al.
Ophthalmic Genetics|December 1, 1996
Full characterization of the maculopathy associated with an Arg-172-Trp mutation in the RDS/peripherin geneB Piguet, E Héon, F L Munier, et al.
Gynecologic Oncology Reports|September 14, 2019
Sixteen year-old with leiomyosarcoma in a prior benign myomectomy siteJennifer A Vaz, Payam Katebi Kashi, Saeid Movahedi-Lankarani, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 29, 1998
Photodynamic therapy of subfoveal choroidal neovascularization: clinical and angiographic examplesU Schmidt-Erfurth, J Miller, M Sickenberg, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 1, 1996
Linkage of autosomal dominant radial drusen (malattia leventinese) to chromosome 2p16-21E Héon, B Piguet, F Munier, et al.
Nature Genetics|June 16, 1999
A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophyE M Stone, A J Lotery, F L Munier, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|September 25, 1999
Photodynamic therapy with verteporfin for choroidal neovascularization caused by age-related macular degeneration: results of a single treatment in a phase 1 and 2 studyJ W Miller, U Schmidt-Erfurth, M Sickenberg, et al.
Pageof 6

Showing results (41-50 of 52) with videos related to

Sort By:
Pageof 6
Eye (London, England)|March 27, 2002
Symptomatic abnormalities of dark adaptation in patients with EFEMP1 retinal dystrophy (Malattia Leventinese/Doyne honeycomb retinal dystrophy)R Haimovici, J Wroblewski, B Piguet, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|May 1, 1997
Age-related macular disease in rural southern ItalyS Pagliarini, A Moramarco, R P Wormald, et al.
Ophthalmic Genetics|November 12, 1998
Rhodopsin C110Y mutation causes a type 2 autosomal dominant retinitis pigmentosaE Millá, E Héon, P A Grounauer, et al.
Ophthalmology|September 1, 1994
Bilateral macular drusen in age-related macular degeneration. Prognosis and risk factorsF G Holz, T J Wolfensberger, B Piguet, et al.
Ophthalmic Genetics|December 1, 1996
Full characterization of the maculopathy associated with an Arg-172-Trp mutation in the RDS/peripherin geneB Piguet, E Héon, F L Munier, et al.
Gynecologic Oncology Reports|September 14, 2019
Sixteen year-old with leiomyosarcoma in a prior benign myomectomy siteJennifer A Vaz, Payam Katebi Kashi, Saeid Movahedi-Lankarani, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 29, 1998
Photodynamic therapy of subfoveal choroidal neovascularization: clinical and angiographic examplesU Schmidt-Erfurth, J Miller, M Sickenberg, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 1, 1996
Linkage of autosomal dominant radial drusen (malattia leventinese) to chromosome 2p16-21E Héon, B Piguet, F Munier, et al.
Nature Genetics|June 16, 1999
A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophyE M Stone, A J Lotery, F L Munier, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|September 25, 1999
Photodynamic therapy with verteporfin for choroidal neovascularization caused by age-related macular degeneration: results of a single treatment in a phase 1 and 2 studyJ W Miller, U Schmidt-Erfurth, M Sickenberg, et al.
Pageof 6