Literature DB >> 4543623

Hereditary alpha1-antitrypsin deficiency and liver cirrhosis in children.

P A Ostergaard.   

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Year:  1973        PMID： 4543623

Source DB:  PubMed          Journal:  Dan Med Bull        ISSN： 0907-8916


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  4 in total

1.  'Durate variant with clinical signs' has alpha1 -antitrypsin genotype ZZ.

Authors:  L R Weitkamp; J W Sayre; R H Schwartz; R Doherty; S A Khera
Journal:  J Med Genet       Date:  1976-02       Impact factor: 6.318

2.  Fine structural observations of the liver in alpha-1-antitrypsin deficiency.

Authors:  E J Yunis; R M Agostini; R H Glew
Journal:  Am J Pathol       Date:  1976-02       Impact factor: 4.307

3.  Outcome of liver disease associated with alpha 1 antitrypsin deficiency (PiZ). Implications for genetic counselling and antenatal diagnosis.

Authors:  H T Psacharopoulos; A P Mowat; P J Cook; P A Carlile; B Portmann; C H Rodeck
Journal:  Arch Dis Child       Date:  1983-11       Impact factor: 3.791

4.  Alpha-1-antitrypsin levels and clinical symptoms in forty-eight children with selective IgA deficiency.

Authors:  P A Ostergaard
Journal:  Eur J Pediatr       Date:  1984-09       Impact factor: 3.183
  4 in total

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