(Q30571110)

15 August 2017

Iranian hereditary hemochromatosis patients: baseline characteristics, laboratory data and gene mutations (English)

1 reference

Seyed-Mohammad Fereshtehnejad

15 August 2017

4

object named as

Seyed-Mohammad Fereshtehnejad

0 references

author name string

Farhad Zamani

1

1 reference

15 August 2017

Zohreh Bagheri

2

1 reference

15 August 2017

Maryam Bayat

3

1 reference

15 August 2017

Ali Basi

5

1 reference

15 August 2017

Hossein Najmabadi

6

1 reference

15 August 2017

Hossein Ajdarkosh

7

1 reference

15 August 2017

1 October 2012

1 reference

15 August 2017

Medical Science Monitor

1 reference

15 August 2017

18

1 reference

15 August 2017

10

1 reference

15 August 2017

CR622-9

1 reference

An association study of HFE gene mutation with idiopathic male infertility in the Chinese Han population

15 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560564

Frequency of Two Common HFE Gene Mutations (C282Y and H63D) in a Group of Iranian Patients With Cryptogenic Cirrhosis

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560564

A novel Y231del mutation of HFE in hereditary haemochromatosis provides in vivo evidence that the Huh-7 is a human haemochromatotic cell line

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560564

Low frequency of HFE gene mutations in Croatian patients suspected of having hereditary hemochromatosis.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560564

The diagnosis and management of hereditary haemochromatosis.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560564

Current approach to hemochromatosis

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560564

20 June 2018

Non-HFE haemochromatosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560564

Genetic background of primary iron overload syndromes in Japan

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560564

Hereditary iron overload: update on pathophysiology, diagnosis, and treatment

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560564

Evaluation of iron overload

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560564

Morbidity risk in HFE associated hereditary hemochromatosis C282Y heterozygotes

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560564

Effect of hemochromatosis genotype and lifestyle factors on iron and red cell indices in a community population.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560564

Hereditary hemochromatosis: impact of molecular and iron-based testing on the diagnosis, treatment, and prevention of a common, chronic disease

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560564

A population-based study of the clinical expression of the hemochromatosis gene

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560564

The effect of HFE mutations on serum ferritin and transferrin saturation in the Jersey population

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560564

Global prevalence of putative haemochromatosis mutations

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560564

Mutation analysis of the HLA-H gene in Italian hemochromatosis patients

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560564

Practice guideline development task force of the College of American Pathologists. Hereditary hemochromatosis

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560564

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560564

An algorithm for the grading of activity in chronic hepatitis C. The METAVIR Cooperative Study Group

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560564

A simple salting out procedure for extracting DNA from human nucleated cells

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560564

Mutations in HFE causing hemochromatosis are associated with primary hypertriglyceridemia

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560564

Hemochromatosis gene (HFE) mutations in patients with type 2 diabetes and their control group in an Iranian population

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560564

Serum measures of iron status and HFE gene mutations in patients with hepatitis B virus infection.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560564

Population screening for haemochromatosis: a unifying analysis of published intervention trials

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560564

Frequency of HFE gene mutations in Iranian beta-thalassaemia minor patients

26 November 2018

1 reference

12 December 2020

Haemochromatosis, HFE and genetic complexity

1 reference

12 December 2020

C282Y and H63D mutations of the haemochromatosis gene in patients with iron overload

1 reference

12 December 2020

Prevalence of HFE (hemochromatosis) gene mutations C282Y and H63D in a Romanian population

1 reference

12 December 2020

Case report of HFE gene testing for the diagnosis of hereditary hemochromatosis

1 reference

12 December 2020

Clinical aspects of hemochromatosis

1 reference

12 December 2020

Hereditary hemochromatosis: a rare disease in Iran

1 reference

12 December 2020

Identification of a novel mutation in the HAMP gene that causes non-detectable hepcidin molecules in a Japanese male patient with juvenile hemochromatosis

1 reference

12 December 2020

Screening for hemochromatosis in primary care settings

1 reference

12 December 2020

Hepatic pathology in relatives of patients with hæmochromatosis

1 reference

12 December 2020

Asymptomatic hemochromatosis subjects: genotypic and phenotypic profiles

1 reference

12 December 2020

Diagnosis of hemochromatosis

1 reference

12 December 2020

A population-based study of the biochemical and clinical expression of the H63D hemochromatosis mutation

1 reference

12 December 2020

Heterogeneity of hemochromatosis in Italy

1 reference

12 December 2020

Identifiers

1 reference

15 August 2017

PubMed publication ID

23018356

1 reference