Evolution of ocular clinical and electrophysiological findings in pediatric Bardet-Biedl syndrome. (Q51969814)

From Wikidata

Jump to navigation Jump to search

scientific article published in January 1999

edit

Language	Label	Description	Also known as
English	Evolution of ocular clinical and electrophysiological findings in pediatric Bardet-Biedl syndrome.	scientific article published in January 1999

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11196121

retrieved

19 April 2018

reference URL

http://europepmc.org/abstract/MED/11196121

title

Evolution of ocular clinical and electrophysiological findings in pediatric Bardet-Biedl syndrome. (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11196121

retrieved

19 April 2018

reference URL

http://europepmc.org/abstract/MED/11196121

main subject

electrophysiology

1 reference

based on heuristic

inferred from title

Bardet-Biedl syndrome

1 reference

based on heuristic

inferred from title

author

Renato Borgatti

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11196121

retrieved

19 April 2018

reference URL

http://europepmc.org/abstract/MED/11196121

Uberto Pozzoli

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11196121

retrieved

19 April 2018

reference URL

http://europepmc.org/abstract/MED/11196121

author name string

E Spaggiari

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11196121

retrieved

19 April 2018

reference URL

http://europepmc.org/abstract/MED/11196121

R Salati

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11196121

retrieved

19 April 2018

reference URL

http://europepmc.org/abstract/MED/11196121

P Nicolini

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11196121

retrieved

19 April 2018

reference URL

http://europepmc.org/abstract/MED/11196121

F Polenghi

series ordinal

6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11196121

retrieved

19 April 2018

reference URL

http://europepmc.org/abstract/MED/11196121

publication date

1 January 1999

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11196121

retrieved

19 April 2018

reference URL

http://europepmc.org/abstract/MED/11196121

published in

International Ophthalmology

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11196121

retrieved

19 April 2018

reference URL

http://europepmc.org/abstract/MED/11196121

volume

23

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11196121

retrieved

19 April 2018

reference URL

http://europepmc.org/abstract/MED/11196121

issue

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11196121

retrieved

19 April 2018

reference URL

http://europepmc.org/abstract/MED/11196121

page(s)

61-67

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11196121

retrieved

19 April 2018

reference URL

http://europepmc.org/abstract/MED/11196121

cites work

Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mapping

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11196121

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bardet-Biedl syndrome is linked to DNA markers on chromosome 11q and is genetically heterogeneous.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11196121

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Macular lesions associated with retinitis pigmentosa

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11196121

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A fifth locus for Bardet-Biedl syndrome maps to chromosome 2q31

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11196121

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A pair of siblings with adiposo-genital dystrophy. 1922.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11196121

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11196121

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Four cases of "retinitis pigmentosa" occurring in the same family, and accompanied by general imperfections of development. 1866.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11196121

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic heterogeneity of Bardet-Biedl syndrome in a distinct Canadian population: evidence for a fifth locus

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11196121

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bardet-Biedl syndrome and related disorders

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11196121

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Spectrum of Renal Disease in Laurence–Moon–Biedl Syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11196121

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Use of a DNA pooling strategy to identify a human obesity syndrome locus on chromosome 15

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11196121

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Progressive cone-rod degeneration

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11196121

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

On congenital obesity syndrome with polydactyly and retinitis pigmentosa (a contribution to the study of clinical forms of hypophyseal obesity). 1920.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11196121

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage of Bardet-Biedl syndrome to chromosome 16q and evidence for non-allelic genetic heterogeneity

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11196121

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparison of visual acuity measured with Allen figures and Snellen letters using the B-VAT II monitor

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11196121

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The association of retinitis pigmentosa with preretinal macular gliosis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11196121

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Early diagnosis of Bardet-Biedl syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11196121

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The ocular phenotype of the Bardet-Biedl syndrome. Comparison to non-syndromic retinitis pigmentosa

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11196121

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Electroretinographic alterations in the Laurence-Moon-Bardet-Biedl phenotype

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11196121

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ocular findings in the Laurence-Moon-Bardet-Biedl syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11196121

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The syndrome of Laurence-Moon-Bardet-Biedl and allied diseases in Switzerland. Clinical, genetic and epidemiological studies

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11196121

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Practical notes: presentation of vision tests

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11196121

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Laurence-Moon-Biedl syndrome. Report of two unrelated children less than 3 years of age.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11196121

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Visual function in Laurence-Moon-Bardet-Biedl syndrome. A survey of 26 cases

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11196121

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Laurence-Moon-Biedl syndrome. Six cases of obesity, short stature, mental retardation, small genitalia, and retinitis pigmentosa

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11196121

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Electrophysiological and eye-movement abnormalities in children with the Bardet-Biedl syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11196121

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1023/A:1026560721525

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11196121

retrieved

19 April 2018

reference URL

http://europepmc.org/abstract/MED/11196121

Dimensions Publication ID

1025196142

0 references

PubMed publication ID

11196121

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11196121

retrieved

19 April 2018

reference URL

http://europepmc.org/abstract/MED/11196121

 

Sitelinks

Wikipedia(0 entries)

edit

Wikibooks(0 entries)

edit

Wikinews(0 entries)

edit

Wikiquote(0 entries)

edit

Wikisource(0 entries)

edit

Wikiversity(0 entries)

edit

Wikivoyage(0 entries)

edit

Wiktionary(0 entries)

edit

Multilingual sites(0 entries)

edit

Retrieved from "https://www.wikidata.org/w/index.php?title=Q51969814&oldid=2255021396"