Literature DB >> 8359811

Association between heterozygous alpha 1-antitrypsin deficiency and genetic hemochromatosis.

R Kaserbacher, T Propst, A Propst, I Graziadei, G Judmaier, W Vogel.   

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Year:  1993        PMID： 8359811

Source DB:  PubMed          Journal:  Hepatology        ISSN： 0270-9139            Impact factor:   17.425


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  6 in total

Review 1.  Advances in alpha-1-antitrypsin deficiency liver disease.

Authors:  Jeffrey H Teckman; Ajay Jain
Journal:  Curr Gastroenterol Rep       Date:  2014-01

Review 2.  Role of HFE gene mutations in liver diseases other than hereditary hemochromatosis.

Authors:  H L Bonkovsky; J V Obando
Journal:  Curr Gastroenterol Rep       Date:  1999 Feb-Mar

3.  Increased PiZ gene frequency for alpha 1 antitrypsin in patients with genetic haemochromatosis.

Authors:  A N Elzouki; R Hultcrantz; P Stål; R Befrits; S Eriksson
Journal:  Gut       Date:  1995-06       Impact factor: 23.059

Review 4.  Alpha-1-antitrypsin deficiency: diagnosis, pathophysiology, and management.

Authors:  Jeffrey H Teckman; Douglas Lindblad
Journal:  Curr Gastroenterol Rep       Date:  2006-02

5.  Heterozygosity for the alpha-1-antitrypsin Z allele in cirrhosis is associated with more advanced disease.

Authors:  Benedikt Schaefer; Mattias Mandorfer; André Viveiros; Armin Finkenstedt; Peter Ferenci; Stefan Schneeberger; Herbert Tilg; Heinz Zoller
Journal:  Liver Transpl       Date:  2018-05-14       Impact factor: 5.799

6.  Deficiency of α-1-antitrypsin influences systemic iron homeostasis.

Authors:  Andrew J Ghio; Joleen M Soukup; Judy H Richards; Bernard M Fischer; Judith A Voynow; Donald E Schmechel
Journal:  Int J Chron Obstruct Pulmon Dis       Date:  2013-01-22
  6 in total

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