The evolving role of visual electrodiagnostics.

Por Heckenlively, J. R.
Publicado em 1993

Preserved para-arteriole retinal pigment epithelium (PPRPE) in retinitis pigmentosa.

Por Heckenlively, J R
Publicado em 1982

RP cone-rod degeneration.

Por Heckenlively, J R
Publicado em 1987

New concept: treating nonproliferative diabetic retinopathy with light adaptation of rods during sleep

Por Heckenlively, J R
Publicado em 2011

Retrospective study of hyperabnormal (supranormal) electroretinographic responses in 104 patients.

Por Heckenlively, J R, Tanji, T, Logani, S
Publicado em 1994

Autosomal dominant retinitis pigmentosa: a log quotient analysis of the photopic and scotopic b-wave amplitude.

Por Iijima, H, Martin, D A, Heckenlively, J R
Publicado em 1989

Nerve fibre layer loss in diseases of the outer retinal layer.

Por Newman, N M, Stevens, R A, Heckenlively, J R
Publicado em 1987

Molecular genetics of retinitis pigmentosa.

Por Farber, D. B., Heckenlively, J. R., Sparkes, R. S., Bateman, J. B.
Publicado em 1991

Investigations of antiretinal antibodies in pigmentary retinopathy and other retinal degenerations.

Por Heckenlively, J R, Aptsiauri, N, Nusinowitz, S, Peng, C, Hargrave, P A
Publicado em 1996

HLA typing in retinitis pigmentosa.

Por Heckenlively, J R, Bastek, J V, Pearlman, J T, Gladden, J, Terasaki, P
Publicado em 1981

Autoimmunity in hereditary retinal degenerations. II. Clinical studies: antiretinal antibodies and fluorescein angiogram findings.

Por Heckenlively, J R, Solish, A M, Chant, S M, Meyers-Elliott, R H
Publicado em 1985

X-linked dominant cone-rod degeneration: linkage mapping of a new locus for retinitis pigmentosa (RP 15) to Xp22.13-p22.11.

Por McGuire, R E, Sullivan, L S, Blanton, S H, Church, M W, Heckenlively, J R, Daiger, S P
Publicado em 1995

Mouse model for Usher syndrome: linkage mapping suggests homology to Usher type I reported at human chromosome 11p15.

Por Heckenlively, J R, Chang, B, Erway, L C, Peng, C, Hawes, N L, Hageman, G S, Roderick, T H
Publicado em 1995

Probable genetic linkage between autosomal dominant retinitis pigmentosa (RP) and amylase (AMY2): evidence of an RP locus on chromosome 1.

Por Spence, M A, Sparkes, R S, Heckenlively, J R, Pearlman, J T, Zedalis, D, Sparkes, M, Crist, M, Tideman, S
Publicado em 1977

A tight linkage cluster, with two new RFLPs (D8S96 and D8S108), in the interval 8cen-q13.

Por Cottingham, A W, Sadler, L A, Blanton, S H, Wagner, M J, Wells, D E, Heckenlively, J R, Daiger, S P
Publicado em 1992

Retrospective, longitudinal, and cross sectional study of visual acuity impairment in choroideraemia

Por Roberts, M Flynn, Fishman, G A, Roberts, D K, Heckenlively, J R, Weleber, R G, Anderson, R J, Grover, S
Publicado em 2002

Map refinement of locus RP13 to human chromosome 17p13.3 in a second family with autosomal dominant retinitis pigmentosa.

Por Kojis, T. L., Heinzmann, C., Flodman, P., Ngo, J. T., Sparkes, R. S., Spence, M. A., Bateman, J. B., Heckenlively, J. R.
Publicado em 1996

A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor gene.

Por Sohocki, M M, Sullivan, L S, Mintz-Hittner, H A, Birch, D, Heckenlively, J R, Freund, C L, McInnes, R R, Daiger, S P
Publicado em 1998

Linkage analysis of five pedigrees affected with typical autosomal dominant retinitis pigmentosa.

Por Field, L L, Heckenlively, J R, Sparkes, R S, Garcia, C A, Farson, C, Zedalis, D, Sparkes, M C, Crist, M, Tideman, S, Spence, M A
Publicado em 1982

Rhodopsin mutations in autosomal dominant retinitis pigmentosa.

Por Sung, C H, Davenport, C M, Hennessey, J C, Maumenee, I H, Jacobson, S G, Heckenlively, J R, Nowakowski, R, Fishman, G, Gouras, P, Nathans, J
Publicado em 1991