(Q38532977)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8488920%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

title

Longitudinal study of the early electroretinographic changes in Alström's syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8488920%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

author name string

F Tremblay

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8488920%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

R G LaRoche

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8488920%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

S E Shea

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8488920%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

M D Ludman

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8488920%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

language of work or name

English

0 references

publication date

1 May 1993

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8488920%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Ophthalmology

13 October 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8488920%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

volume

115

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8488920%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8488920%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

page(s)

657-665

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8488920%20AND%20SRC:MED&resulttype=core&format=json

Familial syndrome of primary testicular insufficiency with normal virilization, blindness, deafness and metabolic abnormalities

13 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971466-7

The Alström syndrome: ophthalmic histopathology and retinal ultrastructure

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971466-7

Alstrom's syndrome: further evidence of autosomal recessive inheritance and endocrinological dysfunction

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971466-7

Electroretinographic assessment of background adaptation in 10-week-old human infants

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971466-7

Temporal aspects of the electroretinogram

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971466-7

Achromatopsia with amblyopia. I. A clinical and electroretinographical study of 39 cases.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971466-7

Classification of complete and incomplete autosomal recessive achromatopsia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971466-7

7 January 2021

The cone degenerations

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971466-7

Progressive Generalized Cone Dysfunction

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971466-7

Differential diagnosis of typical and atypical congenital achromatopsia. Analysis of a progressive foveal dystrophy and a nonprogressive oligo-cone trichromasy (general cone dysfunction without achromatopsia), both of which at first had been diagnos

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971466-7

Ocular and systemic manifestations of the Bardet-Biedl syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971466-7

Retinal and neurologic findings in the Laurence-Moon-Bardet-Biedl phenotype

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971466-7

Progressive cone-rod degeneration

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971466-7

Rod-cone interactions in the ERG of a patient with Bardet-Biedl syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971466-7

Bardet-Biedl syndrome and related disorders

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971466-7

Visual acuities and dark-adapted thresholds of children with Bardet-Biedl syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971466-7

Standard for clinical electroretinography. International Standardization Committee

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971466-7

inferred from DOI database lookup

7 January 2021

based on heuristic

Patterns of rod and cone dysfunction in Bardet-Biedl syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971466-7

inferred from DOI database lookup

7 January 2021

based on heuristic

Laurence-Moon-Biedl syndrome. Report of an unusual family

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2971466-7

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0002-9394(14)71466-7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8488920%20AND%20SRC:MED&resulttype=core&format=json

13 October 2019

1 reference