Alpha 1 antitrypsin deficiency due to Pi null: clinical presentation and evidence for molecular heterogeneity.

Ítems similars

• Liver damage in a neonate with alpha-1-antitrypsin deficiency due to phenotype PiZ null (Z(-))
  per: Burn, John, et al.
  Publicat: (1982)
• What is Pi (proteinase inhibitor) null or PiQO?: a problem highlighted by the alpha 1 antitrypsin Mheerlen mutation.
  per: Kalsheker, N, et al.
  Publicat: (1992)
• Alpha1 antitrypsin deficiency due to an homozygous PI* Null Q0Cairo mutation: Early onset of pulmonary manifestations and variability of clinical expression
  per: Jouhadi, Zineb, et al.
  Publicat: (2018)
• Intracranial haemorrhage due to vitamin K deficiency associated with alpha-1-antitrypsin deficiency type PiZ.
  per: Fidalgo, I, et al.
  Publicat: (1982)
• Prevalence of PI*Z and PI*S alleles of alpha-1-antitrypsin deficiency in Finland
  per: Häggblom, Jan, et al.
  Publicat: (2015)