Literature DB >> 4547904

Alpha1-antitrypsin deficiency. Pi genotype ZO, SO and MO.

C B Laurell, T Sveger, C G Ljunggren.   

Abstract

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Year:  1974        PMID： 4547904     DOI： 10.1111/j.1651-2227.1974.tb04876.x

Source DB:  PubMed          Journal:  Acta Paediatr Scand        ISSN： 0001-656X


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  6 in total

1.  The ultrastructure of hepatocytes in alpha-1-antitrypsin deficiency with the genotype Pi--.

Authors:  G Feldmann; J P Martin; R Sesboue; C Ropartz; R Perelman; M Nathanson; P Seringe; J P Benhamou
Journal:  Gut       Date:  1975-10       Impact factor: 23.059

2.  Does alpha-1-antitrypsin P1 null phenotype exist?

Authors:  J P Martin; R Sesboue; R Charlionet; C Ropartz
Journal:  Humangenetik       Date:  1975-11-06

3.  Alpha 1-antitrypsin deficiency caused by the alpha 1-antitrypsin Nullmattawa gene. An insertion mutation rendering the alpha 1-antitrypsin gene incapable of producing alpha 1-antitrypsin.

Authors:  D Curiel; M Brantly; E Curiel; L Stier; R G Crystal
Journal:  J Clin Invest       Date:  1989-04       Impact factor: 14.808

4.  Pediatric gastroenterology 1/1/69-12/31/75: a review. Part II. The liver and biliary tract.

Authors:  A Finley; M Andorsky; M Davidson
Journal:  Am J Dig Dis       Date:  1977-02

5.  Complete absence of serum alpha-1-antitrypsin in conjunction with an apparently normal gene structure.

Authors:  H Muensch; L Gaidulis; F Kueppers; S Y So; G Escano; V J Kidd; S L Woo
Journal:  Am J Hum Genet       Date:  1986-06       Impact factor: 11.025

6.  Mass screening of newborn Swedish infants for alpha antitrypsin deficiency.

Authors:  C B Laurell; T Sveger
Journal:  Am J Hum Genet       Date:  1975-03       Impact factor: 11.025
  6 in total

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