المؤلفون: McDonald, Merry-Lynn N, Cho, Michael H, Sørheim, Inga-Cecilie, Lutz, Sharon M, Castaldi, Peter J, Lomas, David A, Coxson, Harvey O, Edwards, Lisa D, MacNee, William, Vestbo, Jørgen, Yates, Julie C, Agusti, Alvar, Calverley, Peter MA, Celli, Bartolome, Crim, Courtney, Rennard, Stephen I, Wouters, Emiel FM, Bakke, Per, Tal-Singer, Ruth, Miller, Bruce E, Gulsvik, Amund, Casaburi, Richard, Wells, J Michael, Regan, Elizabeth A, Make, Barry J, Hokanson, John E, Lange, Christoph, Crapo, James D, Beaty, Terri H, Silverman, Edwin K, Hersh, Craig P

المصدر: American Journal of Respiratory Cell and Molecular Biology. 51(5)

مصطلحات موضوعية: Biological Sciences, Biomedical and Clinical Sciences, Genetics, Lung, Prevention, Clinical Research, Chronic Obstructive Pulmonary Disease, Human Genome, 2.1 Biological and endogenous factors, Aetiology, Respiratory, Black or African American, Aged, Aged, 80 and over, Chromosomes, Human, Pair 15, Female, Genetic Predisposition to Disease, Genetic Variation, Genome-Wide Association Study, Humans, Hypoxia, Male, Middle Aged, Oximetry, Oxygen, Polymorphism, Single Nucleotide, Prognosis, Pulmonary Disease, Chronic Obstructive, Rest, White People, chronic obstructive pulmonary disease, hypoxemia, pulse oximetry, genome-wide association study, oxygen saturation, Evaluation of COPD Longitudinally to Identify Predictive Surrogate Endpoints and COPDGene Investigators, Cardiorespiratory Medicine and Haematology, Respiratory System, Biochemistry and cell biology, Cardiovascular medicine and haematology

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/5zx1p9rs

المؤلفون: Sørheim, Inga-Cecilie, Bakke, Per, Gulsvik, Amund, Pillai, Sreekumar G., Johannessen, Ane, Gaarder, Per I., Campbell, Edward J., Agustí, Alvar, Calverley, Peter M.A., Donner, Claudio F., Make, Barry J., Rennard, Stephen I., Vestbo, Jørgen, Wouters, Emiel F.M., Paré, Peter D., Levy, Robert D., Coxson, Harvey O., Lomas, David A., Hersh, Craig P., Silverman, Edwin K.

المصدر: In Chest November 2010 138(5):1125-1132

المؤلفون: Amaral, André F.S., Ramasamy, Adaikalavan, Castro-Giner, Francesc, Minelli, Cosetta, Accordini, Simone, Sørheim, Inga Cecilie, Pin, Isabelle, Kogevinas, Manolis, Jõgi, Rain, Balding, David J., Norbäck, Dan, Verlato, Guiseppe, Olivieri, Mario, Probst-Hensch, Nicole, Janson, Christer, Zock, Jan-Paul, Heinrich, Joachim, Jarvis, Deborah L.

الإتاحة: https://hdl.handle.net/1956/10510

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المؤلفون: Sørheim, Inga-Cecilie, Bakke, Per, Gulsvik, Amund, Pillai, Sreekumar G., Johannessen, Ane, Gaaarder, Per I., Campbell, Edward J., Agustí, Alvar, Calverley, Peter M. A., Donner, Claudio F., Make, Barry J., Rennard, Stephen I., Vestbo, Jørgen, Wouters, Emiel F. M., Paré, Peter D., Levy, Robert D., Coxson, Harvey O., Lomas, David A., Hersh, Craig P., Silverman, Edwin K.

المصدر: CHEST; Nov2010, Vol. 138 Issue 5, p1125-1132, 8p, 4 Charts, 1 Graph

مصطلحات موضوعية: PROTEASE inhibitors, SERUM, ALPHA 1-antitrypsin, OBSTRUCTIVE lung diseases, GENETIC carriers

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عنوان ترانسليتريتد: Genetikk ved kronisk obstruktiv lungesykdom.

المؤلفون: Sørheim IC; Lungeavdelingen, Haukeland universitetssykehus, 5021 Bergen, Norway. inga.cecilie.soerheim@helse-bergen.no, Gulsvik A, Bakke PS, Brøgger JC, Grydeland TB, Silverman EK

المصدر: Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke [Tidsskr Nor Laegeforen] 2009 Oct 22; Vol. 129 (20), pp. 2104-7.

نوع المنشور: Journal Article; Review

بيانات الدورية: Publisher: Norske Laegeforening Country of Publication: Norway NLM ID: 0413423 Publication Model: Print Cited Medium: Internet ISSN: 0807-7096 (Electronic) Linking ISSN: 00292001 NLM ISO Abbreviation: Tidsskr Nor Laegeforen Subsets: MEDLINE

مواضيع طبية MeSH: Pulmonary Disease, Chronic Obstructive/*genetics, Amyloid beta-Protein Precursor/genetics ; Forced Expiratory Volume ; Genetic Predisposition to Disease ; Humans ; Mutation ; Phenotype ; Protease Nexins ; Pulmonary Disease, Chronic Obstructive/etiology ; Pulmonary Disease, Chronic Obstructive/physiopathology ; Receptors, Cell Surface/genetics ; alpha 1-Antitrypsin Deficiency/complications ; alpha 1-Antitrypsin Deficiency/genetics