Genotyping diagnosis of alpha-1 antitrypsin deficiency in Saudi adults with liver cirrhosis. - Wikidata - wikimedia - TriplyDB

Genotyping diagnosis of alpha-1 antitrypsin deficiency in Saudi adults with liver cirrhosis.

Genotyping diagnosis of alpha-1 antitrypsin deficiency in Saudi adults with liver cirrhosis.

http://www.wikidata.org/entity/Q37646702

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The prevalence of PI*S and PI*Z SERPINA1 alleles in healthy individuals and COPD patients in Saudi Arabia: A case-control study.Alpha1 antitrypsin deficiency due to an homozygous PI* Null Q0Cairo mutation: Early onset of pulmonary manifestations and variability of clinical expression.

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Genotyping diagnosis of alpha-1 antitrypsin deficiency in Saudi adults with liver cirrhosis.

http://www.wikidata.org/entity/Q37646702

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on February 2017

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Genotyping diagnosis of alpha- ...... i adults with liver cirrhosis.

@en

Genotyping diagnosis of alpha- ...... i adults with liver cirrhosis.

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type

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Genotyping diagnosis of alpha- ...... i adults with liver cirrhosis.

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Genotyping diagnosis of alpha- ...... i adults with liver cirrhosis.

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prefLabel

Genotyping diagnosis of alpha- ...... i adults with liver cirrhosis.

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Genotyping diagnosis of alpha- ...... i adults with liver cirrhosis.

@nl

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Genotyping diagnosis of alpha- ...... i adults with liver cirrhosis.

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Ahlam Buhairan

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Amina A Hassan

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Basmah Al-Maarik

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Iman Al-Ajeyan

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Maram Al-Otaiby

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Noura Al-Jameil

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Rana Hassanato

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Sree R Isac

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P2860

Diagnosing α1-antitrypsin deficiency: how to improve the current algorithm

The Role and Importance of Glycosylation of Acute Phase Proteins with Focus on Alpha-1 Antitrypsin in Acute and Chronic Inflammatory Conditions

Alpha-1-antitrypsin phenotypes in adult liver disease patients.

The discovery of α1-antitrypsin and its role in health and disease.

Role of alpha-1-antichymotrypsin deficiency in promoting cirrhosis in two siblings with heterozygous alpha-1-antitrypsin deficiency phenotype SZ.

Key current clinical issues in alpha-1 antitrypsin deficiency.

Alpha1-antitrypsin deficiency. 4: Molecular pathophysiology

Rapid and inexpensive detection of alpha1-antitrypsin deficiency-related alleles S and Z by a real-time polymerase chain reaction suitable for a large-scale population-based screening

Clinical heterogeneity and potential high pathogenicity of the Mmalton Alpha 1 antitrypsin allele at the homozygous, compound heterozygous and heterozygous states.

Heterozygous alpha-I antitrypsin deficiency as a co-factor in the development of chronic liver disease: a review.

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e6071

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10.1097/MD.0000000000006071

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2017-02-01T00:00:00Z

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liver cirrhosis

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