(Q34549247)

3 August 2017

title

Idiopathic hemochromotosis and alpha-1-antitrypsin deficiency: coexistence in a family with progressive liver disease in the proband (English)

1 reference

alpha-1-antitrypsin deficiency

3 August 2017

main subject

1 reference

7

T E Starzl

1 reference

3 August 2017

S Anand

1

1 reference

3 August 2017

R R Schade

2

1 reference

3 August 2017

C Bendetti

3

1 reference

3 August 2017

R Kelly

4

1 reference

3 August 2017

B S Rabin

5

1 reference

3 August 2017

J Krause

6

1 reference

3 August 2017

S Iwatsuki

8

1 reference

3 August 2017

D H Van Thiel

9

1 reference

3 August 2017

language of work or name

English

0 references

publication date

1 September 1983

1 reference

3 August 2017

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3 August 2017

volume

3

1 reference

3 August 2017

issue

5

1 reference

3 August 2017

page(s)

714-718

1 reference

Idiopathic hemochromatosis: a study of biochemical expression in 247 heterozygous members of 63 families: evidence for a single major HLA-linked gene

3 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3033118

Liver transplantation for advanced liver disease with alpha-1-antitrypsin deficiency

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3033118

Hemochromatosis: 1980 update.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3033118

Four-year-old children with alpha 1-antitrypsin deficiency. Clinical follow-up and parental attitudes towards neonatal screening.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3033118

Danazol-induced augmentation of serum alpha 1-antitrypsin levels in individuals with marked deficiency of this antiprotease

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3033118

Method for the determination of unsaturated iron-binding capacity of serum using radioactive iron and magnesium carbonate

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3033118

An immunoradiometric assay for ferritin in the serum of normal subjects and patients with iron deficiency and iron overload

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3033118

Heredity of idiopathic haemochromatosis: a study of 106 families

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3033118

Preferential Transmission of the Z Deficient Allele of α 1 -Antitrypsin

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3033118

Pi-Z Phenotypes in a Pulmonary Clinic: Their Prevalence and Physiologic State

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3033118

Alpha-antitrypsin deficiency. Experience from an autopsy material

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3033118

Histocompatibility antigens as markers of abnormal iron metabolism in idiopathic hemochromatosis

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3033118

Histocompatibility antigens as markers of abnormal iron metabolism in patients with idiopathic haemochromatosis and their relatives

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3033118

A new method for determination of alpha-1-antitrypsin phenotypes using isoelectric focusing on polyacrylamide gel slabs

7 July 2018

1 reference

12 December 2020

Alpha-1-antitrypsin deficiency. Phenotype study of 60 members of the same family

1 reference

12 December 2020

Idiopathic hemochromatosis. Demonstration of recessive transmission and early detection by family HLA typing

1 reference

12 December 2020

Smoking and intermediate alpha1-antitrypsin deficiency and lung function in middle-aged men

1 reference

12 December 2020

Heterozygous MZ alpha 1-antitrypsin deficiency in adults with chronic active hepatitis and cryptogenic cirrhosis

1 reference

12 December 2020

Alpha 1-antitrypsin deficiency and liver disease

1 reference

12 December 2020

Macro and micro methods for the determination of serum iron and iron-binding capacity

1 reference

12 December 2020

Identifiers

PMC publication ID

3033118

1 reference

3 August 2017

1 reference