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1

Advances in Night Vision Technology

Berson, Eliot L.

Journal:

Archives of Ophthalmology

Year:

1973

Language:

english

File:

PDF, 777 KB

english, 1973

2

Dominant Leber congenital amaurosis, cone-rod degeneration, and retinitis pigmentosa caused by mutant versions of the transcription factor CRX

Carlo Rivolta, Eliot L. Berson, Thaddeus P. Dryja

Journal:

Year:

2001

Language:

english

File:

PDF, 254 KB

english, 2001

3

Reduction of hyperornithinemia with a low protein, low arginine diet and pyridoxine in patients with a deficiency of ornithine-ketoacid transaminase (OKT) activity and gyrate atrophy of the choroid and retina

Vivian E. Shih, Eliot L. Berson, Marita Gargiulo

Journal:

Clinica Chimica Acta

Year:

1981

Language:

english

File:

PDF, 615 KB

english, 1981

4

Comprehensive screening of the USH2A gene in Usher syndrome type II and non-syndromic recessive retinitis pigmentosa

Babak Jian Seyedahmadi, Carlo Rivolta, Julia A. Keene, Eliot L. Berson, Thaddeus P. Dryja

Journal:

Experimental Eye Research

Year:

2004

Language:

english

File:

PDF, 125 KB

english, 2004

5

Retinitis pigmentosa

Dyonne T Hartong, Eliot L Berson, Thaddeus P Dryja

Journal:

Year:

2006

Language:

english

File:

PDF, 359 KB

english, 2006

6

Transgenic mice with a rhodopsin mutation (Pro23His): A mouse model of autosomal dominant retinitis pigmentosa

Olsson, Jane E., Gordon, Jon W., Pawlyk, Basil S., Roof, Dorothy, Hayes, Annmarie, Molday, Robert S., Mukai, Shizuo, Cowley, Glenn S., Berson, Eliot L., Dryja, Thaddeus P.

Journal:

Year:

1992

Language:

english

File:

PDF, 26.27 MB

english, 1992

7

Mutations in the RPE65 Gene in Patients with Autosomal Recessive Retinitis Pigmentosa or Leber Congenital Amaurosis

Hiroyuki Morimura, Gerald A. Fishman, Sandeep A. Grover, Anne B. Fulton, Eliot L. Berson and Thaddeus P. Dryja

Journal:

Proceedings of the National Academy of Sciences

Year:

1998

Language:

english

File:

PDF, 1.29 MB

english, 1998

8

A Homozygous Missense Mutation in the IRBP Gene ( RBP3 ) Associated with Autosomal Recessive Retinitis Pigmentosa

den Hollander, Anneke I., McGee, Terri L., Ziviello, Carmela, Banfi, Sandro, Dryja, Thaddeus P., Gonzalez-Fernandez, Federico, Ghosh, Debashis, Berson, Eliot L.

Journal:

Investigative Ophthalmology & Visual Science

Year:

2009

Language:

english

File:

PDF, 958 KB

english, 2009

9

Novel frameshift mutations in CRX associated with Leber congenital amaurosis

Carlo Rivolta, Naomi E. Peck, Anne B. Fulton, Gerald A. Fishman, Eliot L. Berson, Thaddeus P. Dryja

Journal:

Year:

2001

Language:

english

File:

PDF, 31 KB

english, 2001

10

Cone cGMP-gated channel mutations and clinical findings in patients with achromatopsia, macular degeneration, and other hereditary cone diseases

Koji M. Nishiguchi, Michael A. Sandberg, Nasim Gorji, Eliot L. Berson, Thaddeus P. Dryja

Journal:

Year:

2005

Language:

english

File:

PDF, 326 KB

english, 2005

11

Variation in retinitis pigmentosa-11 (PRPF31 or RP11) gene expression between symptomatic and asymptomatic patients with dominant RP11 mutations

Carlo Rivolta, Terri L. McGee, Thomas Rio Frio, Roderick V. Jensen, Eliot L. Berson, Thaddeus P. Dryja

Journal:

Year:

2006

Language:

english

File:

PDF, 271 KB

english, 2006

12

A single-base substitution within an intronic repetitive element causes dominant retinitis pigmentosa with reduced penetrance

Thomas Rio Frio, Terri L. McGee, Nicholas M. Wade, Christian Iseli, Jacques S. Beckmann, Eliot L. Berson, Carlo Rivolta

Journal:

Year:

2009

Language:

english

File:

PDF, 321 KB

english, 2009

13

Next generation sequencing of pooled samples reveals new SNRNP200 mutations associated with retinitis pigmentosa

Paola Benaglio, Terri L. McGee, Leonardo P. Capelli, Shyana Harper, Eliot L. Berson, Carlo Rivolta

Journal:

Year:

2011

Language:

english

File:

PDF, 258 KB

english, 2011

14

Retinitis pigmentosa and allied diseases: applications of electroretinographic testing

Eliot L. Berson

Journal:

International Ophthalmology

Year:

1981

Language:

english

File:

PDF, 2.27 MB

english, 1981

15

Extended wearing trial of Trifield lens device for ‘tunnel vision’

Russell L. Woods, Robert G. Giorgi, Eliot L. Berson, Eli Peli

Journal:

Ophthalmic and Physiological Optics

Year:

2010

Language:

english

File:

PDF, 452 KB

english, 2010

16

10.1038/10305

Pierce, Eric A., Quinn, Tracey, Meehan, Terrence, McGee, Terri L., Berson, Eliot L., Dryja, Thaddeus P.

Journal:

Nature Genetics

Year:

1999

Language:

english

File:

PDF, 632 KB

english, 1999

17

Cone Dominance of the Human Early Receptor Potential

GOLDSTEIN, E. BRUCE, BERSON, ELIOT L.

Journal:

Year:

1969

File:

PDF, 248 KB

1969

18

A point mutation of the rhodopsin gene in one form of retinitis pigmentosa

Dryja, Thaddeus P., McGee, Terri L., Reichel, Elias, Hahn, Lauri B., Cowley, Glenn S., Yandell, David W., Sandberg, Michael A., Berson, Eliot L.

Journal:

Year:

1990

File:

PDF, 384 KB

1990

19

Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa

Kajiwara, Kazuto, Hahn, Lauri B., Mukai, Shizuo, Travis, Gabriel H., Berson, Eliot L., Dryja, Thaddeus P.

Journal:

Year:

1991

File:

PDF, 561 KB

1991

20

10.1038/70499

Morimura, Hiroyuki, Saindelle-Ribeaudeau, Florence, Berson, Eliot L, Dryja, Thaddeus P

Journal:

Nature Genetics

Year:

1999

Language:

english

File:

PDF, 135 KB

english, 1999

21

10.1038/70496

Morimura, Hiroyuki, Saindelle-Ribeaudeau, Florence, Berson, Eliot L, Dryja, Thaddeus P

Journal:

Nature Genetics

Year:

1999

Language:

english

File:

PDF, 291 KB

english, 1999

22

10.1038/9707

Dryja, Thaddeus P., Yamamoto, Hiroyuki, Simon, András, Eriksson, Ulf, Harris, Eddie, Berson, Eliot L.

Journal:

Nature Genetics

Year:

1999

Language:

english

File:

PDF, 280 KB

english, 1999

23

Defects in RGS9 or its anchor protein R9AP in patients with slow photoreceptor deactivation

Nishiguchi, Koji M., Sandberg, Michael A., Kooijman, Aart C., Martemyanov, Kirill A., Pott, Jan W. R., Hagstrom, Stephanie A., Arshavsky, Vadim Y., Berson, Eliot L., Dryja, Thaddeus P.

Journal:

Year:

2004

Language:

english

File:

PDF, 277 KB

english, 2004

24

Insights from retinitis pigmentosa into the roles of isocitrate dehydrogenases in the Krebs cycle

Hartong, Dyonne T, Dange, Mayura, McGee, Terri L, Berson, Eliot L, Dryja, Thaddeus P, Colman, Roberta F

Journal:

Nature Genetics

Year:

2008

Language:

english

File:

PDF, 308 KB

english, 2008

25

Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness

Yamamoto, Shuji, Sippel, Kimberly C., Berson, Eliot L., Dryja, Thaddeus P.

Journal:

Nature Genetics

Year:

1997

File:

PDF, 593 KB

1997

26

Recessive mutations in the gene encoding the tubby-like protein TULP1 in patients with Retinitis pigmentosa

North, Michael A., Nishina, Patsy M., Berson, Eliot L., Dryja, Thaddeus P., Hagstrom, Stephanie A.

Journal:

Nature Genetics

Year:

1998

File:

PDF, 369 KB

1998

27

A null mutation in the human peripherin/RDS gene in a family with autosomal dominant retinitis punctata albescens

Kajiwara, Kazuto, Sandberg, Michael A., Berson, Eliot L., Dryja, Thaddeus P.

Journal:

Nature Genetics

Year:

1993

File:

PDF, 590 KB

1993

28

A Null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa

Rosenfeld, Philip J., Cowley, Glenn S., McGee, Terri L., Sandberg, Michael A., Berson, Eliot L., Dryja, Thaddeus P.

Journal:

Nature Genetics

Year:

1992

File:

PDF, 573 KB

1992

29

Recessive mutations in the gene encoding the β–subunit of rod phosphodiesterase in patients with retinitis pigmentosa

McLaughlin, Margaret E., Sandberg, Michael A., Berson, Eliot L., Dryja, Thaddeus P.

Journal:

Nature Genetics

Year:

1993

File:

PDF, 579 KB

1993

30

Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness

Dryja, Thaddeus P., Berson, Eliot L., Rao, Vikram R., Oprian, Daniel D.

Journal:

Nature Genetics

Year:

1993

File:

PDF, 367 KB

1993

31

Autosomal recessive retinitis pigmentosa caused by mutations in the α subunit of rod cGMP phosphodiesterase

Huang, Sherleen H., Pittler, Steven J., Huang, Xizhong, Oliveira, Luanne, Berson, Eliot L., Dryja, Thaddeus P.

Journal:

Nature Genetics

Year:

1995

File:

PDF, 489 KB

1995

32

A Missense Mutation in PRPF6 Causes Impairment of pre-mRNA Splicing and Autosomal-Dominant Retinitis Pigmentosa

Goranka Tanackovic, Adriana Ransijn, Carmen Ayuso, Shyana Harper, Eliot L. Berson, Carlo Rivolta

Journal:

The American Journal of Human Genetics

Year:

2011

Language:

english

File:

PDF, 860 KB

english, 2011

33

ERG Abnormalities in Relation to Histopathologic Findings in Vitiligo Mutant Mice

MAISY TANG, BASIL S PAWLYK, BELA KOSARAS, ELIOT L BERSON, RICHARD L SIDMAN

Journal:

Experimental Eye Research

Year:

1997

Language:

english

File:

PDF, 1.12 MB

english, 1997

34

Evaluation of the Rhodopsin Kinase Gene in Patients with Retinitis Pigmentosa

SHUJI YAMAMOTO, SHAHROKH C KHANI, ELIOT L BERSON, THADDEUS P DRYJA

Journal:

Experimental Eye Research

Year:

1997

Language:

english

File:

PDF, 243 KB

english, 1997

35

Evaluation of the Myosin VIIA Gene and Visual Function in Patients with Usher Syndrome Type I

Amitabh K Bharadwaj, Joseph P Kasztejna, Syed Huq, Eliot L Berson, Thaddeus P Dryja

Journal:

Experimental Eye Research

Year:

2000

Language:

english

File:

PDF, 152 KB

english, 2000

36

Further Screening of the Rhodopsin Gene in Patients with Autosomal Dominant Retinitis Pigmentosa

Rajani Vaithinathan, Eliot L. Berson, Thaddeus P. Dryja

Journal:

Year:

1994

File:

PDF, 158 KB

1994

37

Taurine uptake in isolated retinas of normal rats and rats with hereditary retinal degeneration

Susan Y. Schmidt, Eliot L. Berson

Journal:

Experimental Eye Research

Year:

1978

Language:

english

File:

PDF, 583 KB

english, 1978

38

Analysis of the DNA of patients with retinitis pigmentosa with a cellular retinaldehyde binding protein cDNA

Paul R. Cotran, Peter J. Ringens, John W. Crabb, Eliot L. Berson, Thaddeus P. Dryja

Journal:

Experimental Eye Research

Year:

1990

Language:

english

File:

PDF, 539 KB

english, 1990

39

Genetic analysis of patients with retinitis pigmentosa using a cloned cDNA probe for the human gamma subunit of cyclic GMP phosphodiesterase

Paul R. Cotran, Gail A.P. Bruns, Eliot L. Berson, Thaddeus P. Dryja

Journal:

Experimental Eye Research

Year:

1991

Language:

english

File:

PDF, 1.43 MB

english, 1991

40

Mapping of the human cone transducin α-subunit (GNAT2) gene to 1p13 and negative mutation analysis in patients with Stargardt disease

Ivana Magovcevic, Stanislawa Weremowicz, Cynthia C. Morton, Shao-Ling Fong, Eliot L. Berson, Thaddeus P. Dryja

Journal:

Year:

1995

Language:

english

File:

PDF, 304 KB

english, 1995

41

Histologic study of retinitis pigmentosa due to a mutation in the RP13 gene (PRPC8): comparison with rhodopsin Pro23His, Cys110Arg, and Glu181Lys

King To, Michael Adamian, Eliot L. Berson

Journal:

American Journal of Ophthalmology

Year:

2004

Language:

english

File:

PDF, 494 KB

english, 2004

42

Disease Course of Patients With Pericentral Retinitis Pigmentosa

Michael A. Sandberg, Alexander R. Gaudio, Eliot L. Berson

Journal:

American Journal of Ophthalmology

Year:

2005

Language:

english

File:

PDF, 429 KB

english, 2005

43

Natural Course of Ocular Function in Pigmented Paravenous Retinochoroidal Atrophy

John Y. Choi, Michael A. Sandberg, Eliot L. Berson

Journal:

American Journal of Ophthalmology

Year:

2006

Language:

english

File:

PDF, 1.85 MB

english, 2006

44

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

Michael Adamian, Basil S. Pawlyk, Dong-Hyun Hong, Eliot L. Berson

Journal:

American Journal of Ophthalmology

Year:

2006

Language:

english

File:

PDF, 312 KB

english, 2006

45

Long-term visual prognoses in patients with retinitis pigmentosa: The Ludwig von Sallmann lecture

Eliot L. Berson

Journal:

Experimental Eye Research

Year:

2007

Language:

english

File:

PDF, 1.08 MB

english, 2007

46

Retinal histopathology of an autopsy eye with advanced retinitis pigmentosa in a family with rhodopsin Glu181Lys

King To, Michael Adamian, Thaddeus P Dryja, Eliot L Berson

Journal:

American Journal of Ophthalmology

Year:

2000

Language:

english

File:

PDF, 435 KB

english, 2000

47

Two families from New England with usher syndrome type IC with distinct haplotypes

Margaret M DeAngelis, Terri L McGee, Bronya J.B Keats, Rima Slim, Eliot L Berson, Thaddeus P Dryja

Journal:

American Journal of Ophthalmology

Year:

2001

Language:

english

File:

PDF, 250 KB

english, 2001

48

Melanoma-associated retinopathy and recurrent exudative retinal detachments in a patient with choroidal melanoma

David N Zacks, Michael K Pinnolis, Eliot L Berson, Evangelos S Gragoudas

Journal:

American Journal of Ophthalmology

Year:

2001

Language:

english

File:

PDF, 272 KB

english, 2001

49

Histopathologic study of variation in severity of retinitis pigmentosa due to the dominant rhodopsin mutation Pro23His

King To, Michael Adamian, Thaddeus P Dryja, Eliot L Berson

Journal:

American Journal of Ophthalmology

Year:

2002

Language:

english

File:

PDF, 502 KB

english, 2002

50

Histopathologic and immunohistochemical study of dominant cone degeneration

King To, Michael Adamian, Frederick A. Jakobiec, Eliot L. Berson

Journal:

American Journal of Ophthalmology

Year:

1998

Language:

english

File:

PDF, 975 KB

english, 1998

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