Zobrazeno 1 - 10
of 10
pro vyhledávání: '"alpha 1-antitrypsin deficiency/diagnosis"'
Autor:
Emtiazjoo, A.M., Chandrashekaran, S., Pelaez, A., Alnuaimat, H., Shahmohammadi, A., Machuca, T., Pipkin, M., Golts, E., Yung, G., Floreth, T., Lin, C., Afshar, K.
Publikováno v:
In Journal of Heart and Lung Transplantation April 2019 38(4) Supplement:S327-S327
Autor:
Hassan Alnuaimat, S. Chandrashekaran, A. Emtiazjoo, A. Shahmohammadi, Kamyar Afshar, Gordon L. Yung, Timothy Floreth, Tiago N. Machuca, Eugene Golts, M. Pipkin, C.M. Lin, A. Pelaez
Publikováno v:
The Journal of Heart and Lung Transplantation. 38:S327
Purpose Alpha-1 antitrypsin (AAT) is a significant anti-protease, anti-inflammatory, and immune-regulating protein, which favors organ tolerance after transplantation. Genetic testing for diagnosis of AAT deficiency (AATD) in lung transplant candidat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2f12c39c2c0b3cfb02a09b445fc1874
https://doi.org/10.1016/j.healun.2019.01.826
https://doi.org/10.1016/j.healun.2019.01.826
Autor:
Buist AS; Oregon Health Sciences University, Portland 97201.
Publikováno v:
Lung [Lung] 1990; Vol. 168 Suppl, pp. 543-51.
Autor:
José R Jardim, Francisco Casas-Maldonado, Frederico Leon Arrabal Fernandes, Maria Vera Cruz de O Castellano, María Torres-Durán, Marc Miravitlles
Publikováno v:
Jornal Brasileiro de Pneumologia, Vol 47, Iss 3 (2021)
ABSTRACT Alpha-1 antitrypsin deficiency (AATD) is a rare genetic disorder caused by a mutation in the SERPINA1 gene, which encodes the protease inhibitor alpha-1 antitrypsin (AAT). Severe AATD predisposes individuals to COPD and liver disease. Early
Externí odkaz:
https://doaj.org/article/ac54588edf924b36b07da00fb79d54b0
Autor:
Cristina Valente, J. Gomes, V. Teixeira, C. Guimarães, B.G. Gonçalves, M. Canotilho, Susana Seixas, M.A. Mineiro, C. Antunes, L. Telo, I. Vicente, E. Magalhães, Ruth Caldeira de Melo, D. Maia, F. Costa, Célia Santos, B. Conde, A.P. Lopes, M.E. Brandão, J. Amado, Maria João Oliveira, Maria Sucena, Catarina Sousa
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Pulmonology, Vol 24, Iss, Pp 1-21 (2018)
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Pulmonology, Vol 24, Iss, Pp 1-21 (2018)
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
Alpha-1-antitrypsin deficiency (AATD) is a genetic autosomal codominant disorder caused by mutations in SERPINA1 gene. It is one of the most prevalent genetic disorders, although it remains underdiagnosed. Whereas at international level there are sev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::116e7bb229194d0b57c23beea37a98d3
Autor:
Ignacio Blanco
Blanco's Overview of Alpha-1 Antitrypsin Deficiency: History, Biology, Pathophysiology, Related Diseases, Diagnosis, and Treatment is a robust introduction to topics associated with Alpha-1 Antitrypsin Deficiency (AATD). Included are topics ranging f
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Akademický článek
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This textbook is a practical guide to the application of the philosophy and principles of Integrative and Functional Medical Nutrition Therapy (IFMNT) in the practice of medicine, and the key role nutrition plays in restoring and maintaining wellness