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JRSM Cardiovascular Disease|August 30, 2016
The association between prolongation in QRS duration and presence of coronary collateral circulation in patients with acute myocardial infarctionZülküf Karahan, Bernas Altıntaş, Murat Uğurlu, et al.
Neurogenetics|June 3, 2016
Cortical gene expression: prognostic value for seizure outcome following temporal lobectomy and amygdalohippocampectomyMatthew J Gallek, Jesse Skoch, Tracy Ansay, et al.
BMJ Open|January 14, 2025
Incidence of cancer-related lymphoedema: a protocol for a living systematic review with meta-analysisMelanie Plinsinga, Ben Singh, Kira Bloomquist, et al.
Lymphology|June 1, 1993
Endothelial transdifferentiated phenotype and cell-cycle kinetics of AIDS-associated Kaposi sarcoma cellsD L Way, M H Witte, M Fiala, et al.
Lymphology|March 12, 2010
Lymphedema-distichiasis syndrome without FOXC2 mutation: evidence for chromosome 16 duplication upstream of FOXC2M H Witte, R P Erickson, M Khalil, et al.
Journal of Electrocardiology|June 12, 2019
Prolonged P wave peak time is associated with the severity of coronary artery disease in patients with non-ST segment elevation myocardial infarctionCengiz Burak, Mahmut Yesin, Veysel Ozan Tanık, et al.
Contemporary Clinical Trials|September 8, 2015
Design of a randomized controlled trial to compare debridement to observation of chondral lesions encountered during partial meniscectomy: The ChAMP (Chondral Lesions And Meniscus Procedures) TrialLeslie J Bisson, Melissa A Kluczynski, William M Wind, et al.
The Open Virology Journal|May 15, 2009
HIV-1 Antigens in Neurons of Cocaine-Abusing PatientsMilan Fiala, Elyse J Singer, Deborah Commins, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|April 18, 2025
Protocol for differentiating primary human small airway epithelial cells at the air-liquid interfaceYu Par Aung Myo, Sarah V Camus, Margaret A T Freeberg, et al.
The British Journal of Dermatology|November 22, 2011
Pachyonychia congenita patients with mutations in KRT6A have more extensive disease compared with patients who have mutations in KRT16K M Spaunhurst, A M Hogendorf, F J D Smith, et al.
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