Showing results (741-750 of 1,007) with videos related to
Sort By:
Pageof 101
Annals of Clinical and Translational Neurology|June 8, 2017
A novel design of a Phase III trial of isradipine in early Parkinson disease (STEADY-PD III)Kevin M Biglan, David Oakes, Anthony E Lang, et al.Journal of the American Society of Nephrology : JASN|April 29, 2005
Prediction of acute renal allograft rejection by urinary monokine induced by IFN-gamma (MIG)Ingeborg A Hauser, Sandra Spiegler, Eva Kiss, et al.Translational Psychiatry|December 1, 2017
Genome-wide association study of subcortical brain volume in PTSD cases and trauma-exposed controlsRajendra A Morey, Sarah L Davis, Melanie E Garrett, et al.Archives of Neurology|September 18, 1998
Ropinirole for the treatment of early Parkinson disease: a 12-month experience. Ropinirole Study GroupK D Sethi, C F O'Brien, J P Hammerstad, et al.Paediatric and Perinatal Epidemiology|April 1, 1992
Estimates of the prevalence of childhood seizure disorders in communities where professional resources are scarce: results from Bangladesh, Jamaica and PakistanM S Durkin, L L Davidson, Z M Hasan, et al.Environmental Pollution (Barking, Essex : 1987)|December 5, 2016
Heavy metal contamination in sandy beach macrofauna communities from the Rio de Janeiro coast, Southeastern BrazilTatiana M B Cabrini, Carlos A M Barboza, Viviane B Skinner, et al.Molecular and Cellular Biology|May 1, 1997
Rapid phosphorylation of Ets-2 accompanies mitogen-activated protein kinase activation and the induction of heparin-binding epidermal growth factor gene expression by oncogenic Raf-1S A McCarthy, D Chen, B S Yang, et al.Journal of Cell Science|December 21, 2014
Regulation of Sec16 levels and dynamics links proliferation and secretionKerstin D Tillmann, Veronika Reiterer, Francesco Baschieri, et al.The Journal of Clinical Psychiatry|January 25, 2024
The Clinician's Tardive Inventory (CTI): A New Clinical Tool for Documenting and Rating Tardive DyskinesiaRichard M Trosch, Cynthia L Comella, Stanley N Caroff, et al.American Journal of Human Genetics|November 13, 2002
myotilin Mutation found in second pedigree with LGMD1AMichael A Hauser, Cecilia B Conde, Valeria Kowaljow, et al.Pageof 101