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191 related items for PubMed ID: 2284507
21. Urinary excretion of desmosine (elastin cross-links) in subjects with PiZZ alpha-1-antitrypsin deficiency, a phenotype associated with hereditary predisposition to pulmonary emphysema. Pelham F, Wewers M, Crystal R, Buist AS, Janoff A. Am Rev Respir Dis; 1985 Oct; 132(4):821-3. PubMed ID: 3876794 [Abstract] [Full Text] [Related]
26. [The variability of clinical presentation of chronic obstructive pulmonary disease in patients with hereditary alpha-1 antitrypsin deficiency]. Kuca P, Kamiński D, Campbell E, Kołakowski J, Goljan-Geremek A, Puścińska E, Bieleń P, Nowiński A, Wojda E, Hawryłkiewicz I, Sliwiński P, Górecka D. Pneumonol Alergol Pol; 2004 Dec 15; 72(9-10):420-3. PubMed ID: 16021998 [Abstract] [Full Text] [Related]
37. [Analysis of alpha-1-antitrypsin phenotypes and genotypes in patients with early-onset pulmonary emphysema]. Dwomiczak S, Ziora D, Konofalski L, Szalaty M, Kowalska A, Kozielski J. Pneumonol Alergol Pol; 2005 Nov 10; 73(1):12-7. PubMed ID: 16539178 [Abstract] [Full Text] [Related]
38. [Replacement therapy of emphysema caused by alpha 1-antitrypsin deficiency]. Vidal R, Miravitlles M, de Gracia X, Gallego B, Morell F. Med Clin (Barc); 1991 Feb 09; 96(5):180-2. PubMed ID: 2033989 [Abstract] [Full Text] [Related]