Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Martin H. Welch"'
Autor:
Martin H. Welch, Gary T. Kinasewitz
Publikováno v:
Chest. 120:1057-1058
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b61d1b44d1be3e97a634e9fdfd2a78e2
https://doi.org/10.1378/chest.120.4.1057
https://doi.org/10.1378/chest.120.4.1057
Publikováno v:
Circulation. 43:227-239
Patients with homozygous alpha 1 antitrypsin deficiency present a unique opportunity for evaluation of the pulmonary vasculature in primary emphysema. In five patients, the detailed angiographic appearance of small (0.2-2.0 mm diameter) muscular pulm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9c064e0f76685ad0826188f84a468505
https://doi.org/10.1161/01.cir.43.2.227
https://doi.org/10.1161/01.cir.43.2.227
Publikováno v:
Chest. 72(4)
Evaluation of data from fiberoptic bronchoscopic procedures revealed that for peripheral bronchogenic carcinomas, the diagnostic yield was influenced by the size of the lesion and its distance from the hilum. Failure to diagnose visible carcinomas wa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8098660eafa85c970aa2e88ea95252e
https://pubmed.ncbi.nlm.nih.gov/908215
https://pubmed.ncbi.nlm.nih.gov/908215
Publikováno v:
Chest. 70:641-642
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b078562a5cd50afd139b98342067851a
https://doi.org/10.1378/chest.70.5.641
https://doi.org/10.1378/chest.70.5.641
Publikováno v:
Annals of Internal Medicine. 71:533
Deficiency of serum alpha1antitrypsin is inherited as an autosomal recessive trait, with the homozygous state manifested by severe deficiency and the heterozygous state by intermediate lev...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::161b46b61cddf9e90a4d232f6a98a491
https://doi.org/10.7326/0003-4819-71-3-533
https://doi.org/10.7326/0003-4819-71-3-533