(Q80526548)

English

[Hereditary hemochromatosis, alpha-1-antitrypsin deficiency and Wilson's disease. Pathogenesis, clinical findings and pathways to diagnosis]

scientific article published on 01 February 2008

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18210110%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

[Hereditary hemochromatosis, alpha-1-antitrypsin deficiency and Wilson's disease. Pathogenesis, clinical findings and pathways to diagnosis] (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18210110%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

alpha-1-antitrypsin deficiency

1 reference

based on heuristic

inferred from title

author name string

H Zhou

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18210110%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

H-P Fischer

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18210110%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

publication date

1 February 2008

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18210110%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18210110%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

29

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18210110%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18210110%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

73-83

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18210110%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

https://scigraph.springernature.com/pub.10.1007/s00292-007-0954-2

0 references

α 1 ‐antitrypsin deficiency and liver disease: Clinical presentation, diagnosis and treatment

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Risk of cirrhosis and primary liver cancer in alpha 1-antitrypsin deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alpha-1-antitrypsin deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Liver transplantation in 100 children: Cambridge and King's College Hospital series

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The liver in adolescents with α-antitrypsin deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chronic liver disease in heterozygous alpha1-antitrypsin deficiency PiZ

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Iron as comorbid factor in chronic hepatitis C]

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Long-term substitution in homozygous alpha 1-antitrypsin deficiency. Effect of the proteinase-antiproteinase equilibrium in plasma and sputum]

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Liver changes in heterozygote alpha 1-antitrypsin deficiency PiZ]

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Wilson's Disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Role of liver biopsy in the diagnosis of hepatic iron overload in the era of genetic testing

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Is heterozygous alpha-1-antitrypsin deficiency type PIZ a risk factor for primary liver carcinoma?

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Histopathologic study of the liver in the early cholestatic phase of alpha-1-antitrypsin deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Liver and iron metabolism--a comprehensive hypothesis for the pathogenesis of genetic hemochromatosis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cirrhosis associated with alpha-1-antitrypsin deficiency: a previously unrecognized inherited disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel mutations of the ATP7B gene among 109 Hungarian patients with Wilson's disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular basis of alpha-1-antitrypsin deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alpha 1-antitrypsin deficiency: memorandum from a WHO meeting

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Natural History and Life Expectancy in Severe Alpha1-Antitrypsin Deficiency, Pi Z

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abdominal malignancies in patients with Wilson's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regional distribution of mutations of the ATP7B gene in patients with Wilson disease: impact on genetic testing

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Liver disease and intermediate alpha 1-antitrypsin deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Long-term survival in patients with hereditary hemochromatosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Histological demonstration of copper and copper-associated protein in chronic liver diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cancer risk in patients with hereditary hemochromatosis and in their first-degree relatives

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased risk of chronic liver failure in adults with heterozygous alpha1-antitrypsin deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of the iron-regulatory proteins hemojuvelin and transferrin receptor 2 to the basolateral membrane domain of hepatocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heterozygous alpha 1-antitrypsin phenotypes in patients with end stage liver disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Utility of hepatic iron index in American patients with hereditary hemochromatosis: a multicenter study

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical presentation, diagnosis and long-term outcome of Wilson's disease: a cohort study

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary hemochromatosis--a new look at an old disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Worldwide racial and ethnic distribution of alpha1-antitrypsin deficiency: summary of an analysis of published genetic epidemiologic surveys

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alpha-1 antitrypsin deficiency is not a rare disease but a disease that is rarely diagnosed

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Late-onset Wilson's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lentiviral gene transfer ameliorates disease progression in Long-Evans cinnamon rats: an animal model for Wilson disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary hemochromatosis protein, HFE, interaction with transferrin receptor 2 suggests a molecular mechanism for mammalian iron sensing

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Factors associated with advanced liver disease in adults with alpha1-antitrypsin deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Physical mapping of four serpin genes: alpha 1-antitrypsin, alpha 1-antichymotrypsin, corticosteroid-binding globulin, and protein C inhibitor, within a 280-kb region on chromosome I4q32.1

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Function and regulation of human copper-transporting ATPases

1 reference

https://pubmed.ncbi.nlm.nih.gov/18210110

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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