(Q39787196)

English

Exfoliation syndrome and exfoliation glaucoma-associated LOXL1 variations are not involved in pigment dispersion syndrome and pigmentary glaucoma

scientific article published on 9 July 2008

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

14 September 2017

Exfoliation syndrome and exfoliation glaucoma-associated LOXL1 variations are not involved in pigment dispersion syndrome and pigmentary glaucoma (English)

1 reference

Europe PubMed Central

PMC publication ID

14 September 2017

pigment dispersion syndrome

1 reference

based on heuristic

inferred from title

exfoliation syndrome

1 reference

based on heuristic

inferred from title

author name string

Kollu Nageswara Rao

1

1 reference

Europe PubMed Central

PMC publication ID

14 September 2017

Robert Ritch

2

1 reference

Europe PubMed Central

PMC publication ID

14 September 2017

Syril K Dorairaj

3

1 reference

Europe PubMed Central

PMC publication ID

14 September 2017

Inderjeet Kaur

4

1 reference

Europe PubMed Central

PMC publication ID

14 September 2017

Jeffrey M Liebmann

5

1 reference

Europe PubMed Central

PMC publication ID

14 September 2017

Ravi Thomas

6

1 reference

Europe PubMed Central

PMC publication ID

14 September 2017

Subhabrata Chakrabarti

7

1 reference

Europe PubMed Central

PMC publication ID

14 September 2017

publication date

9 July 2008

1 reference

Europe PubMed Central

PMC publication ID

14 September 2017

Molecular Vision

1 reference

Europe PubMed Central

PMC publication ID

14 September 2017

14

1 reference

Europe PubMed Central

PMC publication ID

14 September 2017

1254-1262

1 reference

Europe PubMed Central

PMC publication ID

14 September 2017

Lysyl oxidase-like protein 1 (LOXL1) gene polymorphisms and exfoliation glaucoma in a Central European population.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447814

22 September 2017

Lack of Association between LOXL1 Variants and Primary Open- Angle Glaucoma in Three Different Populations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447814

22 September 2017

Evaluation of LOXL1 gene polymorphisms in exfoliation syndrome and exfoliation glaucoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447814

22 September 2017

Association of non-synonymous single nucleotide polymorphisms in the LOXL1 gene with pseudoexfoliation syndrome in India

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447814

22 September 2017

Analysis of LOXL1 polymorphisms in a United States population with pseudoexfoliation glaucoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447814

22 September 2017

The molecular pathophysiology of pseudoexfoliation glaucoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447814

22 September 2017

DNA sequence variants in the LOXL1 gene are associated with pseudoexfoliation glaucoma in a U.S. clinic-based population with broad ethnic diversity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447814

22 September 2017

Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447814

22 September 2017

The number of people with glaucoma worldwide in 2010 and 2020

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447814

22 September 2017

Complex genetics of glaucoma susceptibility

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447814

22 September 2017

Haploview: analysis and visualization of LD and haplotype maps

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447814

22 September 2017

Exclusion of chromosome 1q21-q31 from linkage to three pedigrees affected by the pigment-dispersion syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447814

22 September 2017

Combined exfoliation and pigment dispersion syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447814

22 September 2017

Pigmentary dispersion syndrome and pigmentary glaucoma. A prospective study of the natural history.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447814

15 June 2018

Long-term analysis of pigmentary dispersion syndrome and pigmentary glaucoma.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447814

15 June 2018

Risk factors for the development and severity of glaucoma in the pigment dispersion syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447814

15 June 2018

Prevalence of glaucoma. The Beaver Dam Eye Study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447814

15 June 2018

The LOXL1 gene variations are not associated with primary open-angle and primary angle-closure glaucomas.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447814

20 August 2018

Lysyl oxidase-like 1 polymorphisms and exfoliation syndrome in the Japanese population.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447814

20 August 2018

Sensorineural hearing loss in pseudoexfoliation syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447814

20 August 2018

Homocysteine levels in plasma and sensorineural hearing loss in patients with pseudoexfoliation syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447814

20 August 2018

Exfoliation and carotid stiffness

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447814

20 August 2018

The exfoliation syndrome in cognitive impairment of cerebrovascular or Alzheimer's type

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447814

20 August 2018

Combined exfoliation and pigment dispersion: paradigm of an overlap syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447814

20 August 2018

Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic people

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447814

2 December 2018

LOXL1 Mutations Are Associated with Exfoliation Syndrome in Patients from the Midwestern United States

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2447814

2 December 2018

Prevalence of pigment dispersion syndrome in a population undergoing glaucoma screening

1 reference

https://pubmed.ncbi.nlm.nih.gov/18618003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

What is the risk of developing pigmentary glaucoma from pigment dispersion syndrome?

1 reference

https://pubmed.ncbi.nlm.nih.gov/18618003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A gene responsible for the pigment dispersion syndrome maps to chromosome 7q35-q36

1 reference

https://pubmed.ncbi.nlm.nih.gov/18618003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevention of blinking alters iris configuration in pigment dispersion syndrome and in normal eyes

1 reference

https://pubmed.ncbi.nlm.nih.gov/18618003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of LOXL1 common sequence variants in German and Italian patients with pseudoexfoliation syndrome and pseudoexfoliation glaucoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/18618003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Exfoliation syndrome-the most common identifiable cause of open-angle glaucoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/18618003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association Between LOXL1 and pseudoexfoliation

1 reference

https://pubmed.ncbi.nlm.nih.gov/18618003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical features of five pedigrees genetically linked to the juvenile glaucoma locus on chromosome 1q21-q31

1 reference

https://pubmed.ncbi.nlm.nih.gov/18618003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pigmentary dispersion and glaucoma. A new theory

1 reference

https://pubmed.ncbi.nlm.nih.gov/18618003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of LOXL1 gene polymorphisms with pseudoexfoliation in the Japanese

1 reference

https://pubmed.ncbi.nlm.nih.gov/18618003

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 September 2017

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