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22篇 您的检索式：作者名="Weleber RG"

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	题名	作者	年代	出处	被引量
1	Randomized trial of ciliary neurotrophic factor delivered by encapsulated cell intraocular implants for retinitis pigmentosa 显示文摘	Birch DG Weleber RG Duncan JL	2013	Am J Ophthalmol2013，156，2：	1
2	Multifocal electroretinographic evaluation of long-term hydroxychloroquine users显示文摘	Maturi RK Yu M Weleber RG	2004	Arch Ophthalmol2004，122，7：	1
3	Ring-G chromosome, a new G-deletion syndrome? 显示文摘	Weleber RG Hecht F Giblett ER	1968	AmJ Dis Child1968，115，4：	1
4	Treatment of retinal and choroidal degenerations and dystrophies: current status and pros pects for gene based therapy 显示文摘	Weleber RG Kurz DE Trzupek KM	2003	Ophthalmol Clin North Am2003，16，4：	1
5	Muhifocal electroretinographic evaluation of long- term hydroxychloroquine users显示文摘	Maturi RK Yu M Weleber RG	2004	Arch Ophthalmol2004，122，7：	1
6	The effect of age on human cone and rod ganxfeld electroretinograms显示文摘	Weleber RG	1981	Invest Ophthalmol1981，20，：	1
7	An eye for an eye:New modls of genetic ocular disease显示文摘	Evans KG Weleber RG	1997	Nature Biotechnology1997，15，10：	1
8	The effect of age on human cone and rod ganzfeld electroretinograms显示文摘	Weleber RG	1981	Invest Ophthalmol Vis Sci1981，20，：	1
9	Stargardt' s macular dystrophy 显示文摘	Weleber RG	1994	Arch Ophthalmol1994，112，6：	1
10	Randomized trial of ciliary neurotrophic factor delivered by encapsulated cell intraocular implants for retinitis pigmentosa 显示文摘	Birch DG Weleber RG Duncan JL	2013	Am J Ophthalmol2013，156，2：	1
11	Autosomal-dominant congenital cataract associated with a deletion mutation in the human beaded filament protein gene BFSP2 显示文摘	Jakobs PM Hess JF FitzGerald PG Kramer P Weleber RG Litt M	2000	Am J Hum Genet2000，66，4：	1
12	Sperm abnormalities in retinitis pigmentosa显示文摘	Connor WE Weleber RG Defrancesco C	1997	Invest Ophthalmol Vis Sci1997，38，12：	1
13	Molecular biomarkers for auto- immune retinopathies: significance of and-transducin-alpha auto- antibodies显示文摘	Adamus G Brown L Weleber RG	2009	Exp Mol Pathol2009，87，3：	1
14	Autoantibodies against retinal proteins in paraneoplastic and autoimmune retinopathy显示文摘	Adamus G Ren G Weleber RG	2004	BMC Ophthalmol2004，4，：	1
15	A new locus for autosomal dominant congenital cataracts maps to chromosome 3 显示文摘	Kramer PL LaMorticella D Schilling K Billingslea AM Weleber RG Litt M	2000	Invest Ophthalmol Vis Sci2000，41，1：	1
16	Polymorphisms in C2, CFB and C3 are associated with progression to advanced age related macular degeneration associated with visual loss显示文摘	Francis PJ Hamon SC Ott J Weleber RG Klein ML	2009	J Med Genet2009，46，5：	1
17	Mutations in NYX, encoding the leucine-rich proteoglycan nyctalop i n, cause X-linked complete congenital stationary night blindness 显示文摘	Bech-Hansen NT Naylor MJ Maybaum TA Sparkes RL Koop B Birch DG Bergen A A Prinsen CF Polomeno RC Gal A Drack AV Musarella MA Jacobson SG Young RS Weleber RG	2000	Nat G enet2000，26，3：	1
18	Clinical and electrophysiologic characterization of paraneoplastic and autoimmune retinopathies associated with antienolase antibodies 显示文摘	Weleber RG Watzke RC Shults WT	2005	AM J Ophthalmol2005，139，5：	1
19	Stargardt's macular dystrophy (Editorial)显示文摘	Weleber RG	1994	Arch Ophthalmol1994，112，：	1
20	Autosomal-dominant congenital cataract associated with a deletion mutation in the httman beaded filament protein gene BFSP2 显示文摘	Jakobs PM Hess JF FitzGerald PG Kramer P Weleber RG Litt M	2000	Am J Hum Genet2000，66，4：	1

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