(Q37696791)

22 August 2017

10 references

25 April 2019

18 June 2019

20 June 2019

19 June 2019

30 June 2019

14 September 2019

19 September 2019

28 September 2019

15 December 2019

6 November 2020

0 references

Mutations in the HFE gene and sporadic amyotrophic lateral sclerosis risk: a meta-analysis of observational studies (English)

1 reference

amyotrophic lateral sclerosis

22 August 2017

10 references

25 April 2019

18 June 2019

20 June 2019

19 June 2019

30 June 2019

14 September 2019

19 September 2019

28 September 2019

15 December 2019

6 November 2020

1 reference

14 September 2019

biomedical investigative technique

1 reference

19 September 2019

1 reference

28 September 2019

1 reference

15 December 2019

1 reference

6 November 2020

1 reference

M Li

1

1 reference

22 August 2017

L Wang

2

1 reference

22 August 2017

W Wang

3

1 reference

22 August 2017

X L Qi

4

1 reference

22 August 2017

Z Y Tang

5

1 reference

22 August 2017

language of work or name

English

0 references

publication date

18 February 2014

1 reference

Brazilian Journal of Medical and Biological Research

22 August 2017

1 February 2014

10 references

25 April 2019

18 June 2019

20 June 2019

19 June 2019

30 June 2019

14 September 2019

19 September 2019

28 September 2019

15 December 2019

6 November 2020

11 references

22 August 2017

25 April 2019

18 June 2019

20 June 2019

19 June 2019

30 June 2019

14 September 2019

19 September 2019

28 September 2019

15 December 2019

6 November 2020

47

1 reference

22 August 2017

3

1 reference

22 August 2017

215-222

1 reference

Iron accumulation in deep cortical layers accounts for MRI signal abnormalities in ALS: correlating 7 tesla MRI and pathology.

22 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3982942

Current hypotheses for the underlying biology of amyotrophic lateral sclerosis

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3982942

Genes and Environmental Exposures in Veterans with Amyotrophic Lateral Sclerosis: the GENEVA study. Rationale, study design and demographic characteristics.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3982942

Hereditary hemochromatosis--a new look at an old disease

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3982942

Statistical aspects of the analysis of data from retrospective studies of disease

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3982942

Amyotrophic lateral sclerosis

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3982942

Publication and related bias in meta-analysis: power of statistical tests and prevalence in the literature

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3982942

Geography of HFE C282Y and H63D mutations

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3982942

Detection of C282Y and H63D in the HFE gene

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3982942

Bias in meta-analysis detected by a simple, graphical test

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3982942

Global prevalence of putative haemochromatosis mutations

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3982942

Epidemiology of mutations in superoxide dismutase in amyotrophic lateral sclerosis

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3982942

A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3982942

Operating characteristics of a rank correlation test for publication bias

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3982942

Meta-analysis in clinical trials

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3982942

Molecular diagnostic and pathogenesis of hereditary hemochromatosis

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3982942

Clinical diagnosis and management of amyotrophic lateral sclerosis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3982942

Keeping up with genetic discoveries in amyotrophic lateral sclerosis: the ALSoD and ALSGene databases

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3982942

Empirical assessment of effect of publication bias on meta-analyses.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3982942

Influence of HFE variants and cellular iron on monocyte chemoattractant protein-1.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3982942

Increased incidence of the Hfe mutation in amyotrophic lateral sclerosis and related cellular consequences

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3982942

HFE H63D polymorphism is increased in patients with amyotrophic lateral sclerosis of Italian origin

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3982942

Bias in location and selection of studies

23 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3982942

Evidence for nitric oxide-mediated oxidative damage in chronic inflammation. Nitrotyrosine in serum and synovial fluid from rheumatoid patients

23 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3982942

H63D polymorphism in the hemochromatosis gene is associated with sporadic amyotrophic lateral sclerosis in China.

23 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3982942

Random-effects model for meta-analysis of clinical trials: an update

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3982942

Meta-analysis of genetic association studies.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3982942

Clinical features of amyotrophic lateral sclerosis according to the El Escorial and Airlie House diagnostic criteria: A population-based study

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3982942

A population-based study of the effect of the HFE C282Y and H63D mutations on iron metabolism

1 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1590%2F1414-431X20133296

The Association Between H63D Mutations in HFE and Amyotrophic Lateral Sclerosis in a Dutch Population

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1590%2F1414-431X20133296

HFE gene mutations and iron status of Brazilian blood donors

21 January 2018

1 reference

12 December 2020

Association of the H63D polymorphism in the hemochromatosis gene with sporadic ALS

1 reference

12 December 2020

Hemochromatosis genotypes and risk of 31 disease endpoints: meta-analyses including 66,000 cases and 226,000 controls

1 reference

12 December 2020

HFE mutations are not strongly associated with sporadic ALS

1 reference

12 December 2020

H63D polymorphism in HFE is not associated with amyotrophic lateral sclerosis

1 reference

12 December 2020

Hereditary hemochromatosis: mutations in genes involved in iron homeostasis in Brazilian patients

1 reference

12 December 2020

Study of the HFE gene common polymorphisms in French patients with sporadic amyotrophic lateral sclerosis

1 reference

12 December 2020

10.1590/1414-431X20133296

Identifiers

DOI

1 reference

22 August 2017

1 reference

22 August 2017

1 reference