Literature DB >> 4103864

Symptomatic pulmonary emphysema in childhood associated with hereditary alpha-1-antitrypsin and elastase inhibitor deficiency.

R C Talamo, H Levison, M J Lynch, A Hercz, N E Hyslop, H W Bain.   

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Year:  1971        PMID： 4103864     DOI： 10.1016/s0022-3476(71)80053-7

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


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  6 in total

Review 1.  Antitrypsin and the liver.

Authors:  P W Brunt
Journal:  Gut       Date:  1974-07       Impact factor: 23.059

2.  Studies of amniotic fluid and cord blood in an infant with alpha 1-antitrypsin deficiency.

Authors:  D Kaiser; O M Rennert; H W Goedde; H G Benkmann; H Wuilloud; P Kehrli; H Sollberger
Journal:  Humangenetik       Date:  1974

3.  Cockayne's syndrome and emphysema.

Authors:  M Cunningham; S Godfrey; W M Moffat
Journal:  Arch Dis Child       Date:  1978-09       Impact factor: 3.791

4.  [Alpha 1-anti trypsin-deficiency: combination of pulmonary emphysema and liver cirrhosis in infancy (author's transl)].

Authors:  D Kaiser; O M Rennert; H Joller-Jemelka; H Götze; H Sollberger; P Kehrli
Journal:  Klin Wochenschr       Date:  1975-02-01

5.  Pulmonary function in children with homozygous alpha1-protease inhibitor deficiency.

Authors:  W Wiebicke; B Niggemann; A Fischer
Journal:  Eur J Pediatr       Date:  1996-07       Impact factor: 3.183

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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