Cirrose na infância por deficiência de alfa1-antitripsina: relato de caso

Miranda, Esther Castello Branco Mello; Dias, Ísis Martins; Galvão, Jessé Rodrigues; Soares, Manoel do Carmo Pereira; Araújo, Marialva Tereza Ferreira de; Santos, Ney Carneiro dos.
Rev. para. med ; 17(4): 52-58, out.-dez. 2003. ilus
Artículo en Portugués | LILACS | ID: lil-391528

Documentos relacionados

  1. [Alpha-1 antitrypsin deficiency].
  2. Increased Frequency of Heterozygous Alpha-1-Antitrypsin Deficiency in Liver Explants From Nonalcoholic Steatohepatitis Patients.
  3. Probing of the reactive center loop region of alpha-1-antitrypsin by mutagenesis predicts new type-2 dysfunctional variants.
  4. Distribution of alpha1 antitrypsin rare alleles in six countries: Results from the Progenika diagnostic network.
  5. Alpha-1 Antitrypsin Augmentation and the Liver Phenotype of Adults With Alpha-1 Antitrypsin Deficiency (Genotype Pi∗ZZ).
  6. Optimizing the screening of alpha-1 antitrypsin deficiency using serum protein electrophoresis.
  7. [Research progress of hepatocyte transplantation treatment for alpha-1 antitrypsin deficiency].
  8. The Null Q0<sub>Ourém</sub> Variant within a Copy-Neutral Loss-of-Heterozygosity Event Causing Alpha-1 Antitrypsin Deficiency.
  9. Alpha1-antitrypsin deficiency recognized by failure to gain weight in infancy.
  10. Case report of a novel alpha1-antitrypsin null variant in Türkiye: Q0<sub>RIZE</sub>.