Pulmonary A-V Communications in COPD
- 期刊名称Chest
- 作者Jung, Ralph C.; Balchum, Oscar J.
- 卷第88卷
- 期第2期
- 印刷ISSN0012-3692
- 文件大小667.22KB
- 发表时间1985-08
- DOI10.1378/chest.88.2.312a
Lamin A/C mutations associated with familial and sporadic cases of dilated cardiomyopathy in KoreansSong, Kyuyoung; Dube, Marie-Pierre; Lim, Jiyoung; Hwang, Ilsun; Lee, Inchul; Kim, Jae-Joong · Experimental & Molecular Medicine · 2007
A Missense Mutation in the CHRM2 Gene Is Associated With Familial Dilated CardiomyopathyZhang, L.; Hu, A.; Yuan, H.; Cui, L.; Miao, G.; Yang, X.; Wang, L.; Liu, J.; Liu, X.; Wang, S.; Zhang, Z.; Liu, L.; Zhao, R.; Shen, Y. · Circulation Research · 2008
A Novel Mutation in Lamin A/C Causing Familial Dilated Cardiomyopathy Associated With Sudden Cardiac DeathPérez-Serra, Alexandra; Toro, Rocío; Campuzano, Oscar; Sarquella-Brugada, Georgia; Berne, Paola; Iglesias, Anna; Mangas, Alipio; Brugada, Josep; Brugada, Ramon · Journal of Cardiac Failure · 2015
Familial dilated cardiomyopathy and isolated left ventricular noncompaction associated with lamin A/C gene mutationsManuel Hermida-Prieto; Lorenzo Monserrat; Alfonso Castro-Beiras; Rafael Laredo; Rafaela Soler; Jesus Peteiro; Esther Rodríguez; Beatriz Bouzas; Nemesio Álvarez; Javier Muñiz; Marisa Crespo-Leiro · 2004
A Novel α-Tropomyosin Mutation (D55N) Associated with Familial Dilated Cardiomyopathy Increases Tropomyosin Binding to ActinYang, Xiaomei; Recto, Michelle A.; Zhang, Xinyu; Li, Yuejin; Ramirez Correa, Genaro A.; Schmidt, William M.; Murray, Brittney; Murphy, Anne M. · Biophysical Journal · 2019
Familial Dilated Cardiomyopathy Associated With a Novel Combination of Compound Heterozygous TNNC1 VariantsLandim-Vieira, Maicon; Johnston, Jamie R.; Ji, Weizhen; Mis, Emily K.; Tijerino, Joshua; Spencer-Manzon, Michele; Jeffries, Lauren; Hall, E. Kevin; Panisello-Manterola, David; Khokha, Mustafa K.; Deniz, Engin; Chase, P. Bryant; Lakhani, Saquib A.; Pinto, Jose Renato · Frontiers in Physiology · 2020
Familial dilated cardiomyopathy associated with congenital defects in the setting of a novel VCL mutation (Lys815Arg) in conjunction with a known MYPBC3 variantWells, Quinn S.; Ausborn, Natalie L.; Funke, Birgit H.; Pfotenhauer, Jean P.; Fredi, Joseph L.; Baxter, Samantha; DiSalvo, Thomas G.; Hong, Charles C. · Cardiogenetics · 2011
Pneumothorax in the Critically Ill PatientYarmus, Lonny · CHEST Journal · 2012
Recent Advances in Hypersensitivity PneumonitisLacasse, Yves; Girard, Mélissa; Cormier, Yvon · CHEST Journal · 2012
ImmunohistochemistryMani, Haresh; Zander, Dani S. · CHEST Journal · 2012
Update on Sleep and Psychiatric DisordersSateia, Michael J. · CHEST Journal · 2009
The Ethical Foundations of Professionalism <sup>*</sup>Sox, Harold C. · CHEST Journal · 2007
Dynamic Patient CounselingBrown, A. Whitney; Shlobin, Oksana A.; Weir, Nargues; Albano, Maria C.; Ahmad, Shahzad; Smith, Mary; Leslie, Kevin; Nathan, Steven D. · CHEST Journal · 2012
Novel Antiinflammatory Therapies for COPDGross, Nicholas J. · CHEST Journal · 2012
ImmunohistochemistryMani, Haresh; Zander, Dani S. · CHEST Journal · 2012