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Frontiers in Immunology|May 2, 2019
Antigen Extraction and B Cell Activation Enable Identification of Rare Membrane Antigen Specific Human B CellsMaria Zimmermann, Natalie Rose, John M Lindner, et al.
CPT: Pharmacometrics & Systems Pharmacology|June 20, 2019
Recommendations for the Design of Clinical Drug-Drug Interaction Studies With Itraconazole Using a Mechanistic Physiologically-Based Pharmacokinetic ModelYuan Chen, Tamara D Cabalu, Ernesto Callegari, et al.
Clinical Science (London, England : 1979)|March 20, 2013
Low CD34(+) cells, high neutrophils and the metabolic syndrome are associated with an increased risk of venous thromboembolismMarcello Rattazzi, Sabina Villalta, Silvia Galliazzo, et al.
Malaria Journal|December 11, 2012
IL1B, IL4R, IL12RB1 and TNF gene polymorphisms are associated with Plasmodium vivax malaria in BrazilVinicius A Sortica, Maristela G Cunha, Maria Deise O Ohnishi, et al.
Plos One|April 18, 2019
Correction: Absence of pathogenic mutations in CD59 in chronic inflammatory demyelinating polyradiculoneuropathyLena Duchateau, Lorena Martín-Aguilar, Cinta Lleixà, et al.
PLOS Digital Health|August 16, 2023
The role of sex and handedness in the performance of the smartphone-based Finger-Tapping TestFelipe André Costa Brito, Luis Carlos Pereira Monteiro, Enzo Gabriel Rocha Santos, et al.
European Journal of Medicinal Chemistry|September 14, 2015
Δ(5)-Cholenoyl-amino acids as selective and orally available antagonists of the Eph-ephrin systemRiccardo Castelli, Massimiliano Tognolini, Federica Vacondio, et al.
Cerebellum (London, England)|November 18, 2016
Differential Pattern of Cerebellar Atrophy in Tremor-Predominant and Akinetic/Rigidity-Predominant Parkinson's DiseaseCamila Callegari Piccinin, Lidiane Soares Campos, Rachel Paes Guimarães, et al.
World Journal of Surgical Oncology|August 27, 2013
Primary malignant melanoma of the esophagus: a rare and aggressive diseaseFlávio Hiroshi Ananias Morita, Ulysses Ribeiro, Rubens Antonio Aissar Sallum, et al.
Human Genomics|February 14, 2023
The role of genetic testing in the diagnostic workflow of pediatric patients with kidney diseases: the experience of a single institutionTiziana Vaisitti, Valeria Bracciamà, Angelo Corso Faini, et al.
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