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42. [Prolonged jaundice and a heterozygous (PiMZ) alpha 1-antitrypsin deficiency]. Juricić Z Acta Med Iugosl; 1981; 35(2):125-33. PubMed ID: 6972684 [No Abstract] [Full Text] [Related]
43. [Factors increasing susceptibility to neonatal hyaline membrane syndrome. III. Hypercoagulability and failure of the fibrinolytic system. Deficiency of alpha-1 antitrypsin and infection]. Uszyński M; Uszyńska-Folejewska R Pediatr Pol; 1977 Dec; 52(12):1423-6. PubMed ID: 305026 [No Abstract] [Full Text] [Related]
44. Genetics of alpha 1-antitrypsin deficiency in relation to neonatal liver disease. Povey S Mol Biol Med; 1990 Apr; 7(2):161-72. PubMed ID: 2188061 [TBL] [Abstract][Full Text] [Related]
45. ["M" alpha-1-antitrypsin at term of pregnancy in an African population: concentration and microheterogeneity]. Houvet D; Brettes JP; Sangaret M; Clerc M Ann Biol Clin (Paris); 1980; 38(1):9-14. PubMed ID: 6246828 [TBL] [Abstract][Full Text] [Related]
46. Alpha 1-antitrypsin deficiency: the spectrum of pathology and pathophysiology. Cutz E; Cox DW Perspect Pediatr Pathol; 1979; 5():1-39. PubMed ID: 231756 [No Abstract] [Full Text] [Related]
47. [Determination of alpha 2-macroglobulin and alpha 1-antitrypsin in amniotic fluid using laser nephelometry]. Tatra G; Mattausch M; Reinthaller A Z Geburtshilfe Perinatol; 1985; 189(6):255-8. PubMed ID: 2418594 [TBL] [Abstract][Full Text] [Related]
56. The prevention and management of autosomal recessive conditions. Main example: alpha 1-antitrypsin deficiency. Gustavson KH Clin Genet; 1989 Nov; 36(5):327-32. PubMed ID: 2689003 [TBL] [Abstract][Full Text] [Related]
57. Prenatal diagnosis of alpha-1-antitrypsin deficiency by PCR of linked polymorphisms: a study of 17 cases. Abbott CM; Lovegrove JU; Whitehouse DB; Hopkinson DA; Povey S Prenat Diagn; 1993 Jun; 13(6):544. PubMed ID: 8372083 [No Abstract] [Full Text] [Related]