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ÚLTIMOS ARTÍCULOS DISPONIBLES

Genética

Altered human neutrophil FcyRI and FcyRIII but not FcyRII expression is associated with the acute coronary event in patients with coronary artery disease
Na Zhao, Lan Mi, Yaping Zhang, Na Li, Jiaojiao Xu, Dongyu Xia, Junkui Wang, Yue Wu, Xiaojun Liu
Coron. Artery. Dis. 2017 Jan; 28(1). 63-69. DOI: 10.1097/MCA.0000000000000425

Diagnosis and management of adult hereditary cardio-neuromuscular disorders: A model for the multidisciplinary care of complex genetic disorders
R. Brian Sommerville MD, Margherita Guzzi Vincenti BS, Kathleen Winborn RN, BSN, Anne Casey RN, BSN, Nathan O. Stitziel MD, PhD, Anne M. Connolly MD, Douglas L. Mann MD
Trends. Cardiovasc. Med. 2017 Jan; 27(1). 51-58. DOI: 10.1016/j.tcm.2016.06.005

Diagnostic algorithm for familial chylomicronemia syndrome
Erik Stroes, Philippe Moulin, Klaus G. Parhofer, Vinciane Rebours, J-Matthias Löhr, Maurizio Averna
Atheroscler. Suppl. 2017 Jan; 23. 1-7. DOI: 10.1016/j.atherosclerosissup.2016.10.002

DUOX2 Gene Mutation Manifesting as Resistance to Thyrotropin Phenotype
Panudda Srichomkwun, Junta Takamatsu, Deborah A. Nickerson, Michael J. Bamshad, Jessica X. Chong, Samuel Refetoff
Thyroid. 2017 Jan; 26(1). 129-131. DOI: 10.1089/thy.2016.0469

Epigenetic Regulation of the Thermogenic Adipose Program
Audrey Sambeat, Olga Gulyaeva, Jon Dempersmier, Hei Sook Sul
Trends. Endocrinol. Metab. 2017 Jan; 28(1). 19-31. DOI: 10.1016/j.tem.2016.09.003

Future considerations based on the information from Barrter’s and Gitelman’s syndromes
Hadas Alfandary, Daniel Landau
Curr. Opin. Nephrol. Hypertens. 2017 Jan; 26(1). 9-13. DOI: 10.1097/MNH.0000000000000285

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