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Eliot Berson

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Laura C Horton; Eliot L Berson; Matthew P Frosch; Mark G Vangel; Carol Weigel-DiFranco; Jeremy D Schmahmann
Spinocerebellar ataxia type 7: clinical course, phenotype-genotype correlations, and neuropathology.
Eliot L Berson; Bernard Rosner; Michael A Sandberg; Carol Weigel-DiFranco; Walter C Willett
ω-3 Intake in patients with retinitis pigmentosa receiving vitamin A-Reply.
Anthony B Daniels; J Fielding Hejtmancic; Michael A Sandberg; Carol Weigel-DiFranco; Jianjun Chen; Eliot L Berson
Genotype-phenotype correlations in Bardet-Biedl syndrome.

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2013: Laura C Horton; Eliot L Berson; Matthew P Frosch; Mark G Vangel; Carol Weigel-DiFranco; Jeremy D Schmahmann
Spinocerebellar ataxia type 7: clinical course, phenotype-genotype correlations, and neuropathology.
Cerebellum (London, England) 2013;12(2):176-93.
2013: Eliot L Berson; Bernard Rosner; Michael A Sandberg; Carol Weigel-DiFranco; Walter C Willett
ω-3 Intake in patients with retinitis pigmentosa receiving vitamin A-Reply.
JAMA ophthalmology 2013;131(2):267-8.
2012: Anthony B Daniels; J Fielding Hejtmancic; Michael A Sandberg; Carol Weigel-DiFranco; Jianjun Chen; Eliot L Berson
Genotype-phenotype correlations in Bardet-Biedl syndrome.
Archives of ophthalmology 2012;130(7):901-7.
2012: Eliot L Berson; Bernard Rosner; Michael A Sandberg; Carol Weigel-DiFranco; Walter C Willett
ω-3 intake and visual acuity in patients with retinitis pigmentosa receiving vitamin A.
Archives of ophthalmology 2012;130(6):707-11.
2011: Emorfily Potsidis; Eliot L Berson; Michael A Sandberg
Disease course of patients with unilateral pigmentary retinopathy.
Investigative ophthalmology & visual science 2011;52(12):9244-9.
2011: Paola Benaglio; Terri L McGee; Leonardo P Capelli; Shyana Harper; Eliot L Berson; C Rivolta
Next generation sequencing of pooled samples reveals new SNRNP200 mutations associated with retinitis pigmentosa.
Human mutation 2011;32(6):E2246-58.
2011: Goranka Tanackovic; Adriana Ransijn; Philippe Thibault; Sherif Abou Elela; Roscoe Klinck; Eliot L Berson; Benoit Chabot; Carlo Rivolta
PRPF mutations are associated with generalized defects in spliceosome formation and pre-mRNA splicing in patients with retinitis pigmentosa.
Human molecular genetics 2011;20(11):2116-30.
2011: Goranka Tanackovic; Adriana Ransijn; Carmen Ayuso; Shyana Harper; Eliot L Berson; C Rivolta
A missense mutation in PRPF6 causes impairment of pre-mRNA splicing and autosomal-dominant retinitis pigmentosa.
American journal of human genetics 2011;88(5):643-9.
2011: Michael A Sandberg; Bernard Rosner; Carol Weigel-DiFranco; Eliot L Berson
Lack of scientific rationale for use of valproic acid for retinitis pigmentosa.
The British journal of ophthalmology 2011;95(5):744.
2010: Basil Pawlyk; Oleg V Bulgakov; Xiaoqing Liu; Xiaoyun Xu; Michael Adamian; Xun Sun; Shahrokh C Khani; Eliot L Berson; Michael A Sandberg; Tiansen Li
Replacement gene therapy with a human RPGRIP1 sequence slows photoreceptor degeneration in a murine model of Leber congenital amaurosis.
Human gene therapy 2010;21(8):993-1004.
2010: Terri L McGee; Babak Jian Seyedahmadi; Meredith O Sweeney; Thaddeus P Dryja; Eliot L Berson
Novel mutations in the long isoform of the USH2A gene in patients with Usher syndrome type II or non-syndromic retinitis pigmentosa.
Journal of medical genetics 2010;47(7):499-506.
2010: Russell L Woods; Robert G Giorgi; Eliot L Berson; Eli Peli
Extended wearing trial of Trifield lens device for 'tunnel vision'.
Ophthalmic & physiological optics : the journal of the British College of Ophthalmic Opticians (Optometrists) 2010;30(3):240-52.
2010: Eliot L Berson; Bernard Rosner; Michael A Sandberg; Carol Weigel-DiFranco; Robert J Brockhurst; KC Hayes; Elizabeth J Johnson; Ellen J Anderson; Chris A Johnson; Alexander R Gaudio; Walter C Willett; Ernst J Schaefer
Clinical trial of lutein in patients with retinitis pigmentosa receiving vitamin A.
Archives of ophthalmology 2010;128(4):403-11.
2010: Michael A Sandberg; Elizabeth J Johnson; Eliot L Berson
The relationship of macular pigment optical density to serum lutein in retinitis pigmentosa.
Investigative ophthalmology & visual science 2010;51(2):1086-91.
2010: Demetrios Vavvas; Nancy Huynh; Louis Pasquale; Eliot L Berson
Progressive hydroxychloroquine toxicity mimicking low-tension glaucoma after discontinuation of the drug.
Acta ophthalmologica 2010;88(1):156-7.
2009: Thomas Rio Frio; Terri L McGee; Nicholas M Wade; Christian Iseli; Jacques Beckmann; Eliot L Berson; C Rivolta
A single-base substitution within an intronic repetitive element causes dominant retinitis pigmentosa with reduced penetrance.
Human mutation 2009;30(9):1340-7.
2009: Anneke I den Hollander; Terri L McGee; Carmela Ziviello; Sandro Banfi; Thaddeus P Dryja; Federico Gonzalez-Fernandez; Debashis Ghosh; Eliot L Berson
A homozygous missense mutation in the IRBP gene (RBP3) associated with autosomal recessive retinitis pigmentosa.
Investigative ophthalmology & visual science 2009;50(4):1864-72.
2009: Dyonne T Hartong; Terri L McGee; Michael A Sandberg; Eliot L Berson; Folkert W Asselbergs; Pim van der Harst; Immaculata DeVivo; Thaddeus P Dryja
Search for a correlation between telomere length and severity of retinitis pigmentosa due to the dominant rhodopsin Pro23His mutation.
Molecular vision 2009;15():592-7.
2008: Michael A Sandberg; Bernard Rosner; Carol Weigel-DiFranco; Terri L McGee; Thaddeus P Dryja; Eliot L Berson
Disease course in patients with autosomal recessive retinitis pigmentosa due to the USH2A gene.
Investigative ophthalmology & visual science 2008;49(12):5532-9.
2008: Dyonne T Hartong; Mayura Dange; Terri L McGee; Eliot L Berson; Thaddeus P Dryja; Roberta F Colman
Insights from retinitis pigmentosa into the roles of isocitrate dehydrogenases in the Krebs cycle.
Nature genetics 2008;40(10):1230-4.
2008: Michael A Sandberg; Robert J Brockhurst; Alexander R Gaudio; Eliot L Berson
Visual acuity is related to parafoveal retinal thickness in patients with retinitis pigmentosa and macular cysts.
Investigative ophthalmology & visual science 2008;49(10):4568-72.
2008: Thomas Rio Frio; Nicholas M Wade; Adriana Ransijn; Eliot L Berson; Jacques Beckmann; C Rivolta
Premature termination codons in PRPF31 cause retinitis pigmentosa via haploinsufficiency due to nonsense-mediated mRNA decay.
The Journal of clinical investigation 2008;118(4):1519-31.
2008: Eliot L Berson
Retinal degenerations: planning for the future.
Advances in experimental medicine and biology 2008;613():21-35.
2007: Sureka Thiagalingam; Terri L McGee; Richard G Weleber; Michael A Sandberg; Karmen M Trzupek; Eliot L Berson; Thaddeus P Dryja
Novel mutations in the KCNV2 gene in patients with cone dystrophy and a supernormal rod electroretinogram.
Ophthalmic genetics 2007;28(3):135-42.
2007: Eliot L Berson
Long-term visual prognoses in patients with retinitis pigmentosa: the Ludwig von Sallmann lecture.
Experimental eye research 2007;85(1):7-14.
2007: Michael A Sandberg; Bernard Rosner; Carol Weigel-DiFranco; Thaddeus P Dryja; Eliot L Berson
Disease course of patients with X-linked retinitis pigmentosa due to RPGR gene mutations.
Investigative ophthalmology & visual science 2007;48(3):1298-304.
2007: Meredith O Sweeney; Terri L McGee; Eliot L Berson; Thaddeus P Dryja
Low prevalence of lecithin retinol acyltransferase mutations in patients with Leber congenital amaurosis and autosomal recessive retinitis pigmentosa.
Molecular vision 2007;13():588-93.
2006: Dyonne T Hartong; Eliot L Berson; Thaddeus P Dryja
Retinitis pigmentosa.
Lancet 2006;368(9549):1795-809.
2006: Michael Adamian; Basil Pawlyk; Dong-Hyun Hong; Eliot L Berson
Rod and cone opsin mislocalization in an autopsy eye from a carrier of X-linked retinitis pigmentosa with a Gly436Asp mutation in the RPGR gene.
American journal of ophthalmology 2006;142(3):515-8.
2006: Carlo Rivolta; Terri L McGee; Thomas Rio Frio; Roderick V Jensen; Eliot L Berson; Thaddeus P Dryja
Variation in retinitis pigmentosa-11 (PRPF31 or RP11) gene expression between symptomatic and asymptomatic patients with dominant RP11 mutations.
Human mutation 2006;27(7):644-53.
2006: John Y Choi; Michael A Sandberg; Eliot L Berson
Natural course of ocular function in pigmented paravenous retinochoroidal atrophy.
American journal of ophthalmology 2006;141(4):763-5.
2006: Carlo Rivolta; Eliot L Berson; Thaddeus P Dryja
Mutation screening of the peropsin gene, a retinal pigment epithelium specific rhodopsin homolog, in patients with retinitis pigmentosa and allied diseases.
Molecular vision 2006;12():1511-5.
2006: Geetha H Mylvaganam; Terri L McGee; Eliot L Berson; Thaddeus P Dryja
A screen for mutations in the transducin gene GNB1 in patients with autosomal dominant retinitis pigmentosa.
Molecular vision 2006;12():1496-8.
2005: Michael A Sandberg; Robert J Brockhurst; Alexander R Gaudio; Eliot L Berson
The association between visual acuity and central retinal thickness in retinitis pigmentosa.
Investigative ophthalmology & visual science 2005;46(9):3349-54.
2005: Michael A Sandberg; Alexander R Gaudio; Eliot L Berson
Disease course of patients with pericentral retinitis pigmentosa.
American journal of ophthalmology 2005;140(1):100-6.
2005: Yael Ben-Arie-Weintrob; Eliot L Berson; Thaddeus P Dryja
Histopathologic-genotypic correlations in retinitis pigmentosa and allied diseases.
Ophthalmic genetics 2005;26(2):91-100.
2005: Yuko Wada; Michael A Sandberg; Terri L McGee; Melissa A Stillberger; Eliot L Berson; Thaddeus P Dryja
Screen of the IMPDH1 gene among patients with dominant retinitis pigmentosa and clinical features associated with the most common mutation, Asp226Asn.
Investigative ophthalmology & visual science 2005;46(5):1735-41.
2005: Thaddeus P Dryja; Terri L McGee; Eliot L Berson; Gerald A Fishman; Michael A Sandberg; Kenneth R Alexander; Deborah J Derlacki; Aruna S Rajagopalan
Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6.
Proceedings of the National Academy of Sciences of the United States of America 2005;102(13):4884-9.
2005: Koji M Nishiguchi; Michael A Sandberg; Nasim Gorji; Eliot L Berson; Thaddeus P Dryja
Cone cGMP-gated channel mutations and clinical findings in patients with achromatopsia, macular degeneration, and other hereditary cone diseases.
Human mutation 2005;25(3):248-58.
2004: Koji M Nishiguchi; James S Friedman; Michael A Sandberg; Anand Swaroop; Eliot L Berson; Thaddeus P Dryja
Recessive NRL mutations in patients with clumped pigmentary retinal degeneration and relative preservation of blue cone function.
Proceedings of the National Academy of Sciences of the United States of America 2004;101(51):17819-24.
2004: Koji M Nishiguchi; Izabela Sokal; Lili Yang; Nirmalya Roychowdhury; Krzysztof Palczewski; Eliot L Berson; Thaddeus P Dryja; Wolfgang Baehr
A novel mutation (I143NT) in guanylate cyclase-activating protein 1 (GCAP1) associated with autosomal dominant cone degeneration.
Investigative ophthalmology & visual science 2004;45(11):3863-70.
2004: Eliot L Berson; Bernard Rosner; Michael A Sandberg; Carol Weigel-DiFranco; Ann B Moser; Robert J Brockhurst; KC Hayes; Chris A Johnson; Ellen J Anderson; Alexander R Gaudio; Walter C Willett; Ernst Schaefer
Further evaluation of docosahexaenoic acid in patients with retinitis pigmentosa receiving vitamin A treatment: subgroup analyses.
Archives of ophthalmology 2004;122(9):1306-14.
2004: Eliot L Berson; Bernard Rosner; Michael A Sandberg; Carol Weigel-DiFranco; Ann B Moser; Robert J Brockhurst; KC Hayes; Chris A Johnson; Ellen J Anderson; Alexander R Gaudio; Walter C Willett; Ernst Schaefer
Clinical trial of docosahexaenoic acid in patients with retinitis pigmentosa receiving vitamin A treatment.
Archives of ophthalmology 2004;122(9):1297-305.
2004: Babak Jian Seyedahmadi; Carlo Rivolta; Julia A Keene; Eliot L Berson; Thaddeus P Dryja
Comprehensive screening of the USH2A gene in Usher syndrome type II and non-syndromic recessive retinitis pigmentosa.
Experimental eye research 2004;79(2):167-73.
2004: King To; Michael Adamian; Eliot L Berson
Histologic study of retinitis pigmentosa due to a mutation in the RP13 gene (PRPC8): comparison with rhodopsin Pro23His, Cys110Arg, and Glu181Lys.
American journal of ophthalmology 2004;137(5):946-8.
2004: Koji M Nishiguchi; Eliot L Berson; Thaddeus P Dryja
Mutation screening of the phosducin gene PDC in patients with retinitis pigmentosa and allied diseases.
Molecular vision 2004;10():62-4.
2004: Koji M Nishiguchi; Michael A Sandberg; Aart Kooijman; Kirill Martemyanov; Jan Willem R Pott; Stephanie A Hagstrom; Vadim Y Arshavsky; Eliot L Berson; Thaddeus P Dryja
Defects in RGS9 or its anchor protein R9AP in patients with slow photoreceptor deactivation.
Nature 2004;427(6969):75-8.
2003: Dror Sharon; Michael A Sandberg; Vivian W Rabe; Melissa Stillberger; Thaddeus P Dryja; Eliot L Berson
RP2 and RPGR mutations and clinical correlations in patients with X-linked retinitis pigmentosa.
American journal of human genetics 2003;73(5):1131-46.
2003: Dror Sharon; Michael A Sandberg; Rafael C Caruso; Eliot L Berson; Thaddeus P Dryja
Shared mutations in NR2E3 in enhanced S-cone syndrome, Goldmann-Favre syndrome, and many cases of clumped pigmentary retinal degeneration.
Archives of ophthalmology 2003;121(9):1316-23.
2003: Carlo Rivolta; Radha Ayyagari; Paul Sieving; Eliot L Berson; Thaddeus P Dryja
Evaluation of the ELOVL4 gene in patients with autosomal recessive retinitis pigmentosa and Leber congenital amaurosis.
Molecular vision 2003;9():49-51.
2002: Xuejiao Wang; Siqun Xu; Carlo Rivolta; Lili Y Li; Guang-Hua Peng; Prabodh K Swain; Ching-Hwa Sung; Anand Swaroop; Eliot L Berson; Thaddeus P Dryja; Shiming Chen
Barrier to autointegration factor interacts with the cone-rod homeobox and represses its transactivation function.
The Journal of biological chemistry 2002;277(45):43288-300.
2002: Carlo Rivolta; Eliot L Berson; Thaddeus P Dryja
Paternal uniparental heterodisomy with partial isodisomy of chromosome 1 in a patient with retinitis pigmentosa without hearing loss and a missense mutation in the Usher syndrome type II gene USH2A.
Archives of ophthalmology 2002;120(11):1566-71.
2002: King W To; Charles Thirkill; Frederick A Jakobiec; Simmons Lessell; Eliot L Berson
Lymphoma-associated retinopathy.
Ophthalmology 2002;109(11):2149-53.
2002: Eliot L Berson; Bernard Rosner; Carol Weigel-DiFranco; Thaddeus P Dryja; Michael A Sandberg
Disease progression in patients with dominant retinitis pigmentosa and rhodopsin mutations.
Investigative ophthalmology & visual science 2002;43(9):3027-36.
2002: King To; Michael Adamian; Thaddeus P Dryja; Eliot L Berson
Histopathologic study of variation in severity of retinitis pigmentosa due to the dominant rhodopsin mutation Pro23His.
American journal of ophthalmology 2002;134(2):290-3.
2002: Dror Sharon; Hiroyuki Yamamoto; Terri L McGee; Vivian Rabe; Robert T Szerencsei; Robert J Winkfein; Clemens F M Prinsen; Claire S Barnes; sten andreasson; Gerald A Fishman; Paul P M Schnetkamp; Eliot L Berson; Thaddeus P Dryja
Mutated alleles of the rod and cone Na-Ca+K-exchanger genes in patients with retinal diseases.
Investigative ophthalmology & visual science 2002;43(6):1971-9.
2002: Basil Pawlyk; Tiansen Li; Michael S Scimeca; Michael A Sandberg; Eliot L Berson
Absence of photoreceptor rescue with D-cis-diltiazem in the rd mouse.
Investigative ophthalmology & visual science 2002;43(6):1912-5.
2002: Margaret DeAngelis; Jonna L Grimsby; Michael A Sandberg; Eliot L Berson; Thaddeus P Dryja
Novel mutations in the NRL gene and associated clinical findings in patients with dominant retinitis pigmentosa.
Archives of ophthalmology 2002;120(3):369-75.
2001: Carlo Rivolta; N E Peck; A B Fulton; Gerald A Fishman; Eliot L Berson; Thaddeus P Dryja
Novel frameshift mutations in CRX associated with Leber congenital amaurosis.
Human mutation 2001;18(6):550-1.
2001: Carlo Rivolta; Eliot L Berson; Thaddeus P Dryja
Dominant Leber congenital amaurosis, cone-rod degeneration, and retinitis pigmentosa caused by mutant versions of the transcription factor CRX.
Human mutation 2001;18(6):488-98.
2001: David N Zacks; M K Pinnolis; Eliot L Berson; Evangelos S Gragoudas
Melanoma-associated retinopathy and recurrent exudative retinal detachments in a patient with choroidal melanoma.
American journal of ophthalmology 2001;132(4):578-81.
2001: C E Briggs; D Rucinski; Philip J Rosenfeld; Tatsuo Hirose; Eliot L Berson; Thaddeus P Dryja
Mutations in ABCR (ABCA4) in patients with Stargardt macular degeneration or cone-rod degeneration.
Investigative ophthalmology & visual science 2001;42(10):2229-36.
2001: Eliot L Berson; Jonna L Grimsby; S M Adams; Terri L McGee; E Sweklo; Eric A Pierce; Michael A Sandberg; Thaddeus P Dryja
Clinical features and mutations in patients with dominant retinitis pigmentosa-1 (RP1).
Investigative ophthalmology & visual science 2001;42(10):2217-24.
2001: Thaddeus P Dryja; S M Adams; Jonna L Grimsby; Terri L McGee; Dong-Hyun Hong; T Li; Sten Andréasson; Eliot L Berson
Null RPGRIP1 alleles in patients with Leber congenital amaurosis.
American journal of human genetics 2001;68(5):1295-8.
2001: Margaret DeAngelis; Terri L McGee; Bronya J B Keats; R Slim; Eliot L Berson; Thaddeus P Dryja
Two families from New England with usher syndrome type IC with distinct haplotypes.
American journal of ophthalmology 2001;131(3):355-8.
2001: CA Grant; Eliot L Berson
Treatable forms of retinitis pigmentosa associated with systemic neurological disorders.
International ophthalmology clinics 2001;41(1):103-10.
2000: King To; Michael Adamian; Thaddeus P Dryja; Eliot L Berson
Retinal histopathology of an autopsy eye with advanced retinitis pigmentosa in a family with rhodopsin Glu181Lys.
American journal of ophthalmology 2000;130(6):790-2.
2000: Thaddeus P Dryja; J A McEvoy; Terri L McGee; Eliot L Berson
Novel rhodopsin mutations Gly114Val and Gln184Pro in dominant retinitis pigmentosa.
Investigative ophthalmology & visual science 2000;41(10):3124-7.
2000: Dror Sharon; G A Bruns; Terri L McGee; Michael A Sandberg; Eliot L Berson; Thaddeus P Dryja
X-linked retinitis pigmentosa: mutation spectrum of the RPGR and RP2 genes and correlation with visual function.
Investigative ophthalmology & visual science 2000;41(9):2712-21.
2000: A K Bharadwaj; J P Kasztejna; Syed O Huq; Eliot L Berson; Thaddeus P Dryja
Evaluation of the myosin VIIA gene and visual function in patients with Usher syndrome type I.
Experimental eye research 2000;71(2):173-81.
2000: Carlo Rivolta; E A Sweklo; Eliot L Berson; Thaddeus P Dryja
Missense mutation in the USH2A gene: association with recessive retinitis pigmentosa without hearing loss.
American journal of human genetics 2000;66(6):1975-8.
2000: Dong-Hyun Hong; Basil Pawlyk; J Shang; Michael A Sandberg; Eliot L Berson; Tiansen Li
A retinitis pigmentosa GTPase regulator (RPGR)-deficient mouse model for X-linked retinitis pigmentosa (RP3).
Proceedings of the National Academy of Sciences of the United States of America 2000;97(7):3649-54.
2000: Eliot L Berson
Nutrition and retinal degenerations.
International ophthalmology clinics 2000;40(4):93-111.
1999: H Morimura; F Saindelle-Ribeaudeau; Eliot L Berson; Thaddeus P Dryja
Mutations in RGR, encoding a light-sensitive opsin homologue, in patients with retinitis pigmentosa.
Nature genetics 1999;23(4):393-4.
1999: Michael A Sandberg; Basil Pawlyk; Eliot L Berson
Acuity recovery and cone pigment regeneration after a bleach in patients with retinitis pigmentosa and rhodopsin mutations.
Investigative ophthalmology & visual science 1999;40(10):2457-61.
1999: Thaddeus P Dryja; J McEvoy; Terri L McGee; Eliot L Berson
No mutations in the coding region of the PRKCG gene in three families with retinitis pigmentosa linked to the RP11 locus on chromosome 19q.
American journal of human genetics 1999;65(3):926-8.
1999: Thaddeus P Dryja; D E Rucinski; S H Chen; Eliot L Berson
Frequency of mutations in the gene encoding the alpha subunit of rod cGMP-phosphodiesterase in autosomal recessive retinitis pigmentosa.
Investigative ophthalmology & visual science 1999;40(8):1859-65.
1999: Eric A Pierce; T Quinn; T Meehan; Terri L McGee; Eliot L Berson; Thaddeus P Dryja
Mutations in a gene encoding a new oxygen-regulated photoreceptor protein cause dominant retinitis pigmentosa.
Nature genetics 1999;22(3):248-54.
1999: H Yamamoto; A Simon; U Eriksson; E Harris; Eliot L Berson; Thaddeus P Dryja
Mutations in the gene encoding 11-cis retinol dehydrogenase cause delayed dark adaptation and fundus albipunctatus.
Nature genetics 1999;22(2):188-91.
1999: L Sibulesky; KC Hayes; Andrzej Pronczuk; Carol Weigel-DiFranco; Bernard Rosner; Eliot L Berson
Safety of <7500 RE (<25000 IU) vitamin A daily in adults with retinitis pigmentosa.
The American journal of clinical nutrition 1999;69(4):656-63.
1999: H Morimura; Eliot L Berson; Thaddeus P Dryja
Recessive mutations in the RLBP1 gene encoding cellular retinaldehyde-binding protein in a form of retinitis punctata albescens.
Investigative ophthalmology & visual science 1999;40(5):1000-4.
1999: W Tulvatana; Michael Adamian; Eliot L Berson; Thaddeus P Dryja
Photoreceptor rosettes in autosomal dominant retinitis pigmentosa with reduced penetrance.
Archives of ophthalmology 1999;117(3):399-402.
1999: Eliot L Berson; Frederick A Jakobiec
Neural retinal cell transplantation: ideal versus reality.
Ophthalmology 1999;106(3):445-6.
1998: Tiansen Li; Michael A Sandberg; Basil Pawlyk; Bernard Rosner; KC Hayes; Thaddeus P Dryja; Eliot L Berson
Effect of vitamin A supplementation on rhodopsin mutants threonine-17 --> methionine and proline-347 --> serine in transgenic mice and in cell cultures.
Proceedings of the National Academy of Sciences of the United States of America 1998;95(20):11933-8.
1998: King To; Michael Adamian; Frederick A Jakobiec; Eliot L Berson
Histopathologic and immunohistochemical study of dominant cone degeneration.
American journal of ophthalmology 1998;126(1):140-2.
1998: Michael A Sandberg; Basil Pawlyk; J Dan; B Arnaud; Thaddeus P Dryja; Eliot L Berson
Rod and cone function in the Nougaret form of stationary night blindness.
Archives of ophthalmology 1998;116(7):867-72.
1998: H Morimura; Gerald A Fishman; S A Grover; A B Fulton; Eliot L Berson; Thaddeus P Dryja
Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis.
Proceedings of the National Academy of Sciences of the United States of America 1998;95(6):3088-93.
1998: Kimberly C Sippel; J D DeStefano; Eliot L Berson; Thaddeus P Dryja
Evaluation of the human arrestin gene in patients with retinitis pigmentosa and stationary night blindness.
Investigative ophthalmology & visual science 1998;39(3):665-70.
1998: Stephanie A Hagstrom; M A North; P L Nishina; Eliot L Berson; Thaddeus P Dryja
Recessive mutations in the gene encoding the tubby-like protein TULP1 in patients with retinitis pigmentosa.
Nature genetics 1998;18(2):174-6.
1998: K W To; Michael Adamian; Frederick A Jakobiec; Eliot L Berson
Histopathologic and immunohistochemical study of an autopsy eye with X-linked cone degeneration.
Archives of ophthalmology 1998;116(1):100-3.
1997: Terri L McGee; M Devoto; J Ott; Eliot L Berson; Thaddeus P Dryja
Evidence that the penetrance of mutations at the RP11 locus causing dominant retinitis pigmentosa is influenced by a gene linked to the homologous RP11 allele.
American journal of human genetics 1997;61(5):1059-66.
1997: Thaddeus P Dryja; L B Hahn; K Kajiwara; Eliot L Berson
Dominant and digenic mutations in the peripherin/RDS and ROM1 genes in retinitis pigmentosa.
Investigative ophthalmology & visual science 1997;38(10):1972-82.
1997: S Yamamoto; S C Khani; Eliot L Berson; Thaddeus P Dryja
Evaluation of the rhodopsin kinase gene in patients with retinitis pigmentosa.
Experimental eye research 1997;65(2):249-53.
1997: M Tang; Basil Pawlyk; Bela Kosaras; Eliot L Berson; Richard L Sidman
ERG abnormalities in relation to histopathologic findings in vitiligo mutant mice.
Experimental eye research 1997;65(2):215-22.
1997: A H Parminder; A Murakami; George Inana; Eliot L Berson; Thaddeus P Dryja
Evaluation of the human gene encoding recoverin in patients with retinitis pigmentosa or an allied disease.
Investigative ophthalmology & visual science 1997;38(3):704-9.
1997: S Yamamoto; Kimberly C Sippel; Eliot L Berson; Thaddeus P Dryja
Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness.
Nature genetics 1997;15(2):175-8.
1996: I Magovcevic; Eliot L Berson; Cynthia C Morton
Detection of cone alpha transducin mRNA in human fetal cochlea: negative mutation analysis in Usher syndrome.
Hearing research 1996;99(1-2):7-12.
1996: K W To; Michael Adamian; Frederick A Jakobiec; Eliot L Berson
Clinical and histopathologic findings in clumped pigmentary retinal degeneration.
Archives of ophthalmology 1996;114(8):950-5.
1996: Michael A Sandberg; C Weigel-DiFranco; B Rosner; Eliot L Berson
The relationship between visual field size and electroretinogram amplitude in retinitis pigmentosa.
Investigative ophthalmology & visual science 1996;37(8):1693-8.
1996: Eliot L Berson
Retinitis pigmentosa: unfolding its mystery.
Proceedings of the National Academy of Sciences of the United States of America 1996;93(10):4526-8.
1996: Eliot L Berson; J F Remulla; B Rosner; Michael A Sandberg; C Weigel-DiFranco
Evaluation of patients with retinitis pigmentosa receiving electric stimulation, ozonated blood, and ocular surgery in Cuba.
Archives of ophthalmology 1996;114(5):560-3.
1996: Michael A Sandberg; Basil Pawlyk; Eliot L Berson
Isolation of focal rod electroretinograms from the dark-adapted human eye.
Investigative ophthalmology & visual science 1996;37(5):930-4.
1995: S H Huang; Steven J Pittler; X Huang; L Oliveira; Eliot L Berson; Thaddeus P Dryja
Autosomal recessive retinitis pigmentosa caused by mutations in the alpha subunit of rod cGMP phosphodiesterase.
Nature genetics 1995;11(4):468-71.
1995: Thaddeus P Dryja; J T Finn; Y W Peng; T L McGee; Eliot L Berson; King-Wai Yau
Mutations in the gene encoding the alpha subunit of the rod cGMP-gated channel in autosomal recessive retinitis pigmentosa.
Proceedings of the National Academy of Sciences of the United States of America 1995;92(22):10177-81.
1995: Philip J Rosenfeld; L B Hahn; Michael A Sandberg; Thaddeus P Dryja; Eliot L Berson
Low incidence of retinitis pigmentosa among heterozygous carriers of a specific rhodopsin splice site mutation.
Investigative ophthalmology & visual science 1995;36(11):2186-92.
1995: Michael A Sandberg; C Weigel-DiFranco; Thaddeus P Dryja; Eliot L Berson
Clinical expression correlates with location of rhodopsin mutation in dominant retinitis pigmentosa.
Investigative ophthalmology & visual science 1995;36(9):1934-42.
1995: Ernst Schaefer; S J Robins; George M Patton; M A Sandberg; C A Weigel-DiFranco; B Rosner; Eliot L Berson
Red blood cell membrane phosphatidylethanolamine fatty acid content in various forms of retinitis pigmentosa.
Journal of lipid research 1995;36(7):1427-33.
1995: Thaddeus P Dryja; Eliot L Berson
Retinitis pigmentosa and allied diseases. Implications of genetic heterogeneity.
Investigative ophthalmology & visual science 1995;36(7):1197-200.
1995: Tiansen Li; W K Franson; J W Gordon; Eliot L Berson; Thaddeus P Dryja
Constitutive activation of phototransduction by K296E opsin is not a cause of photoreceptor degeneration.
Proceedings of the National Academy of Sciences of the United States of America 1995;92(8):3551-5.
1995: M E McLaughlin; T L Ehrhart; Eliot L Berson; Thaddeus P Dryja
Mutation spectrum of the gene encoding the beta subunit of rod phosphodiesterase among patients with autosomal recessive retinitis pigmentosa.
Proceedings of the National Academy of Sciences of the United States of America 1995;92(8):3249-53.
1995: I Magovcevic; Stanislawa Weremowicz; Cynthia C Morton; S L Fong; Eliot L Berson; T P Dryja
Mapping of the human cone transducin alpha-subunit (GNAT2) gene to 1p13 and negative mutation analysis in patients with Stargardt disease.
Genomics 1995;25(1):288-90.
1994: Eliot L Berson
Visual function testing: clinical correlations.
Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society 1994;11(5):472-81.
1994: S K Kim; Jonathan L Haines; Eliot L Berson; Thaddeus P Dryja
Nonallelic heterogeneity in autosomal dominant retinitis pigmentosa with incomplete penetrance.
Genomics 1994;22(3):659-660.
1994: K Kajiwara; Eliot L Berson; Thaddeus P Dryja
Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci.
Science (New York, N.Y.) 1994;264(5165):1604-8.
1994: R Vaithinathan; Eliot L Berson; Thaddeus P Dryja
Further screening of the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa.
Genomics 1994;21(2):461-3.
1994: Tiansen Li; Michael Adamian; D J Roof; Eliot L Berson; Thaddeus P Dryja; Blake J Roessler; B L Davidson
In vivo transfer of a reporter gene to the retina mediated by an adenoviral vector.
Investigative ophthalmology & visual science 1994;35(5):2543-9.
1994: L B Hahn; Eliot L Berson; Thaddeus P Dryja
Evaluation of the gene encoding the gamma subunit of rod phosphodiesterase in retinitis pigmentosa.
Investigative ophthalmology & visual science 1994;35(3):1077-82.
1993: Thaddeus P Dryja; Eliot L Berson; V R Rao; Daniel D Oprian
Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness.
Nature genetics 1993;4(3):280-3.
1993: Michael A Sandberg; Michael J Tolentino; S Miller; Eliot L Berson; Alexander R Gaudio
Hyperopia and neovascularization in age-related macular degeneration.
Ophthalmology 1993;100(7):1009-13.
1993: Eliot L Berson; B Rosner; Michael A Sandberg; K C Hayes; B W Nicholson; C Weigel-DiFranco; W Willett
A randomized trial of vitamin A and vitamin E supplementation for retinitis pigmentosa.
Archives of ophthalmology 1993;111(6):761-72.
1993: M E McLaughlin; Michael A Sandberg; Eliot L Berson; Thaddeus P Dryja
Recessive mutations in the gene encoding the beta-subunit of rod phosphodiesterase in patients with retinitis pigmentosa.
Nature genetics 1993;4(2):130-4.
1993: Eliot L Berson
Retinitis pigmentosa. The Friedenwald Lecture.
Investigative ophthalmology & visual science 1993;34(5):1659-76.
1993: K Kajiwara; Michael A Sandberg; Eliot L Berson; Thaddeus P Dryja
A null mutation in the human peripherin/RDS gene in a family with autosomal dominant retinitis punctata albescens.
Nature genetics 1993;3(3):208-12.
1993: K W To; Michael Adamian; Frederick A Jakobiec; Eliot L Berson
Olivopontocerebellar atrophy with retinal degeneration. An electroretinographic and histopathologic investigation.
Ophthalmology 1993;100(1):15-23.
1992: Eliot L Berson; Michael Adamian
Ultrastructural findings in an autopsy eye from a patient with Usher's syndrome type II.
American journal of ophthalmology 1992;114(6):748-57.
1992: G P Matthews; Michael A Sandberg; Eliot L Berson
Foveal cone electroretinograms in patients with central visual loss of unexplained etiology.
Archives of ophthalmology 1992;110(11):1568-70.
1992: jane elizabeth olsson; J W Gordon; Basil Pawlyk; D Roof; A Hayes; R S Molday; Shizuo Mukai; G S Cowley; Eliot L Berson; Thaddeus P Dryja
Transgenic mice with a rhodopsin mutation (Pro23His): a mouse model of autosomal dominant retinitis pigmentosa.
Neuron 1992;9(5):815-30.
1992: Philip J Rosenfeld; G S Cowley; T L McGee; Michael A Sandberg; Eliot L Berson; Thaddeus P Dryja
A null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa.
Nature genetics 1992;1(3):209-13.
1991: K Kajiwara; L B Hahn; Shizuo Mukai; Gabriel H Travis; Eliot L Berson; Thaddeus P Dryja
Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa.
Nature 1991;354(6353):480-3.
1991: A Weiner; Michael A Sandberg; Alexander R Gaudio; M M Kini; Eliot L Berson
Hydroxychloroquine retinopathy.
American journal of ophthalmology 1991;112(5):528-34.
1991: P R Cotran; G A Bruns; Eliot L Berson; Thaddeus P Dryja
Genetic analysis of patients with retinitis pigmentosa using a cloned cDNA probe for the human gamma subunit of cyclic GMP phosphodiesterase.
Experimental eye research 1991;53(5):557-64.
1991: Thaddeus P Dryja; L B Hahn; G S Cowley; T L McGee; Eliot L Berson
Mutation spectrum of the rhodopsin gene among patients with autosomal dominant retinitis pigmentosa.
Proceedings of the National Academy of Sciences of the United States of America 1991;88(20):9370-4.
1991: Eliot L Berson; B Rosner; Michael A Sandberg; C Weigel-DiFranco; Thaddeus P Dryja
Ocular findings in patients with autosomal dominant retinitis pigmentosa and rhodopsin, proline-347-leucine.
American journal of ophthalmology 1991;111(5):614-23.
1991: Eliot L Berson; B Rosner; Michael A Sandberg; Thaddeus P Dryja
Ocular findings in patients with autosomal dominant retinitis pigmentosa and a rhodopsin gene defect (Pro-23-His).
Archives of ophthalmology 1991;109(1):92-101.
1991: Eliot L Berson; Michael A Sandberg; Thaddeus P Dryja
Autosomal dominant retinitis pigmentosa with rhodopsin, valine-345-methionine.
Transactions of the American Ophthalmological Society 1991;89():117-28; discussion 128-30.
1991: Basil Pawlyk; Michael A Sandberg; Eliot L Berson
Effects of IBMX on the rod ERG of the isolated perfused cat eye: antagonism with light, calcium or L-cis-diltiazem.
Vision research 1991;31(7-8):1093-7.
1990: Thaddeus P Dryja; T L McGee; L B Hahn; G S Cowley; jane elizabeth olsson; E Reichel; Michael A Sandberg; Eliot L Berson
Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa.
The New England journal of medicine 1990;323(19):1302-7.
1990: Michael A Sandberg; S Miller; Eliot L Berson
Rod electroretinograms in an elevated cyclic guanosine monophosphate-type human retinal degeneration. Comparison with retinitis pigmentosa.
Investigative ophthalmology & visual science 1990;31(11):2283-7.
1990: P J Ringens; M Fang; T Shinohara; C D Bridges; C L Lerea; Eliot L Berson; Thaddeus P Dryja
Analysis of genes coding for S-antigen, interstitial retinol binding protein, and the alpha-subunit of cone transducin in patients with retinitis pigmentosa.
Investigative ophthalmology & visual science 1990;31(8):1421-6.
1990: P R Cotran; P J Ringens; J W Crabb; Eliot L Berson; Thaddeus P Dryja
Analysis of the DNA of patients with retinitis pigmentosa with a cellular retinaldehyde binding protein cDNA.
Experimental eye research 1990;51(1):15-9.
1990: S Y Schmidt; Eliot L Berson
Opsin phosphorylation in retinas from autopsy eyes with retinitis pigmentosa.
Investigative ophthalmology & visual science 1990;31(6):1023-8.
1990: F J Manning; A M Bruce; Eliot L Berson
Electroretinograms in microcephaly with chorioretinal degeneration.
American journal of ophthalmology 1990;109(4):457-63.
1990: Thaddeus P Dryja; T L McGee; E Reichel; L B Hahn; G S Cowley; D W Yandell; Michael A Sandberg; Eliot L Berson
A point mutation of the rhodopsin gene in one form of retinitis pigmentosa.
Nature 1990;343(6256):364-6.
1990: Eliot L Berson
Ocular findings in a form of retinitis pigmentosa with a rhodopsin gene defect.
Transactions of the American Ophthalmological Society 1990;88():355-88.
1989: E Reichel; A M Bruce; Michael A Sandberg; Eliot L Berson
An electroretinographic and molecular genetic study of X-linked cone degeneration.
American journal of ophthalmology 1989;108(5):540-7.
1988: S Y Schmidt; C A Heth; R B Edwards; J T Brandt; AJ Adler; A Spiegel; Hitoshi Shichi; Eliot L Berson
Identification of proteins in retinas and IPM from eyes with retinitis pigmentosa.
Investigative ophthalmology & visual science 1988;29(11):1585-93.
1988: Eliot L Berson; Simmons Lessell
Paraneoplastic night blindness with malignant melanoma.
American journal of ophthalmology 1988;106(3):307-11.
1988: S O'Gorman; W A Flaherty; Gerald A Fishman; Eliot L Berson
Histopathologic findings in Best's vitelliform macular dystrophy.
Archives of ophthalmology 1988;106(9):1261-8.
1988: Michael A Sandberg; Basil Pawlyk; W G Crane; Eliot L Berson
Diurnal rhythm in the electroretinogram of the Royal College of Surgeons (RCS) pigmented rat.
Experimental eye research 1988;46(6):929-36.
1988: S O Andréasson; Michael A Sandberg; Eliot L Berson
Narrow-band filtering for monitoring low-amplitude cone electroretinograms in retinitis pigmentosa.
American journal of ophthalmology 1988;105(5):500-3.
1988: Michael A Sandberg; C M Baruzzi; A H Hanson; Eliot L Berson
Rod ERG diurnal rhythm in some patients with dominant retinitis pigmentosa.
Investigative ophthalmology & visual science 1988;29(3):494-8.
1987: Michael A Sandberg; Basil Pawlyk; W G Crane; S Y Schmidt; Eliot L Berson
Effects of IBMX on the ERG of the isolated perfused cat eye.
Vision research 1987;27(9):1421-30.
1987: Eliot L Berson
Electroretinographic findings in retinitis pigmentosa.
Japanese journal of ophthalmology 1987;31(3):327-48.
1986: Michael A Sandberg; Basil Pawlyk; Eliot L Berson
Electroretinogram (ERG) sensitivity and phagosome frequency in the normal pigmented rat.
Experimental eye research 1986;43(5):781-9.
1986: Michael A Sandberg; Basil Pawlyk; Eliot L Berson
Full-field electroretinograms in miniature poodles with progressive rod-cone degeneration.
Investigative ophthalmology & visual science 1986;27(7):1179-84.
1985: Eliot L Berson; Michael A Sandberg; B Rosner; David G Birch; A H Hanson
Natural course of retinitis pigmentosa over a three-year interval.
American journal of ophthalmology 1985;99(3):240-51.
1982: Eliot L Berson; A H Hanson; B Rosner; V E Shih
A two year trial of low protein, low arginine diets or vitamin B6 for patients with gyrate atrophy.
Birth defects original article series 1982;18(6):209-18.
1982: Eliot L Berson
Nutrition and retinal degenerations. Vitamin A, taurine, ornithine, and phytanic acid.
Retina (Philadelphia, Pa.) 1982;2(4):236-55.