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Bibliografía
[1.]
A. Capelastegui, J. Ramos González.
Bronquiectasias: etiopatogenia y métodos diagnósticos.
Arch Bronconeumol, 30 (1994), pp. 153-162
[2.]
A.B. Zin, G. Supinski.
Genetic diseases of the pulmonary parenchyma.
Textbook of pulmonary diseases, 4.a, pp. 1.521-1.540
[3.]
M.J. Tobin, C.S. Duncan, B.M. Hutchison.
An overview of the pulmonary features of alfa-l-antitrypsin deficiency.
Arch Intern Med, 142 (1982), pp. 1.342-1.348
[4.]
M.S. Shin, K.J. Ho.
Bronchiectasis in patients with alfa-l-antitripsin deficiency: A rare occurrence?.
Chest, 104 (1993), pp. 1.384-1.386
[5.]
I. Blanco, M.L. Menéndez, F. Carro.
Bronquiectasias extensas como manifestación única de un defecto grave de alfa-1-antitripsina.
Arch Bronconeumol, 28 (1992), pp. 253
[6.]
American Thoracic Society.
Guidelines for the approach to the patient with severe hereditary alpha-l-antitrypsin deficiency.
Am Rev Respir Dis, 140 (1989), pp. 1.494-1.497
Copyright © 1994. Sociedad Española de Neumología y Cirugía Torácica
