Results 151 to 160 of about 13,044 (182)
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Treatment of Alpha-1 Antitrypsin Deficiency
Seminars in Respiratory and Critical Care Medicine, 2015Alpha-1 antitrypsin deficiency (AATD) is a rare genetic disease that creates multiple unique phenotypes of chronic obstructive pulmonary disease. While bronchospasm, cough, dyspnea, and sputum production all occur with AATD, the phenotypic differences require a computed tomographic (CT) scan to decipher.
Charlie, Strange, Tatsiana, Beiko
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Alpha-1-Antitrypsin Deficiency Panniculitis
Dermatologic Clinics, 2008Alpha-1-antitrypsin deficiency is a congenital error of metabolism linked to pulmonary (emphysema) and liver (cirrhosis) disease. Since 1972, panniculitis has been associated with this deficiency, initially related to Weber-Christian syndrome and finally as a differentiated entity.
Ricardo, Valverde +4 more
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MZ Alpha-1 Antitrypsin Deficiency
American Journal of Respiratory and Critical Care Medicine, 2022Oliver J, McElvaney +4 more
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Alpha-1 antitrypsin deficiency
The Nurse Practitioner, 2014Cathy R, Kessenich, Kathryn, Bacher
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Alpha-1-Antitrypsin Deficiency
Clinics in Chest Medicine, 1983S, Idell, A B, Cohen
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Testing Patterns and Disparities for Alpha-1 Antitrypsin Deficiency
American Journal of Medicine, 2023Jorge Lascano, Mark Brantly
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Alpha-1 antitrypsin deficiency–associated panniculitis
Journal of the American Academy of Dermatology, 2022James Ralph +2 more
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Galactosemia and Alpha-1- antitrypsin Deficiency
Clinical Pediatrics, 1985F, Taylor +4 more
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<p>Monocytes and Macrophages in Alpha-1 Antitrypsin Deficiency</p>
International Journal of COPD, 2020Kylie Belchamber +2 more
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Variants of SERPINA1 and the increasing complexity of testing for alpha-1 antitrypsin deficiency
Therapeutic Advances in Chronic Disease, 2021Kimberly Foil
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