Alpha 1 “Hereditary Emphysema” Experience: A Patient–Physician Perspective

This article is co-authored by a patient living with alpha-1 antitrypsin deficiency, and her treating physician. The commentary article describes the patient’s experience of the diagnosis and treatment process. The physician then discusses alpha-1 antitrypsin deficiency diagnosis and management in t...

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Detalles Bibliográficos
Autores principales: Moyer, Katie, Afshar, Kamyar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2020
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7672128/
https://www.ncbi.nlm.nih.gov/pubmed/32519167
http://dx.doi.org/10.1007/s41030-020-00119-4
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author Moyer, Katie
Afshar, Kamyar
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Afshar, Kamyar
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description This article is co-authored by a patient living with alpha-1 antitrypsin deficiency, and her treating physician. The commentary article describes the patient’s experience of the diagnosis and treatment process. The physician then discusses alpha-1 antitrypsin deficiency diagnosis and management in the context of the patient’s experiences.
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spelling pubmed-76721282020-11-20 Alpha 1 “Hereditary Emphysema” Experience: A Patient–Physician Perspective Moyer, Katie Afshar, Kamyar Pulm Ther Review This article is co-authored by a patient living with alpha-1 antitrypsin deficiency, and her treating physician. The commentary article describes the patient’s experience of the diagnosis and treatment process. The physician then discusses alpha-1 antitrypsin deficiency diagnosis and management in the context of the patient’s experiences. Springer Healthcare 2020-06-09 /pmc/articles/PMC7672128/ /pubmed/32519167 http://dx.doi.org/10.1007/s41030-020-00119-4 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Review
Moyer, Katie
Afshar, Kamyar
Alpha 1 “Hereditary Emphysema” Experience: A Patient–Physician Perspective
title Alpha 1 “Hereditary Emphysema” Experience: A Patient–Physician Perspective
title_full Alpha 1 “Hereditary Emphysema” Experience: A Patient–Physician Perspective
title_fullStr Alpha 1 “Hereditary Emphysema” Experience: A Patient–Physician Perspective
title_full_unstemmed Alpha 1 “Hereditary Emphysema” Experience: A Patient–Physician Perspective
title_short Alpha 1 “Hereditary Emphysema” Experience: A Patient–Physician Perspective
title_sort alpha 1 “hereditary emphysema” experience: a patient–physician perspective
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7672128/
https://www.ncbi.nlm.nih.gov/pubmed/32519167
http://dx.doi.org/10.1007/s41030-020-00119-4
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