Login

Lauren Glenn

ORCID: 0000-0003-0263-4149
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
A5071106457
Research Areas
  • Atrial Fibrillation Management and Outcomes
  • Injury Epidemiology and Prevention
  • Poisoning and overdose treatments
  • Neurogenetic and Muscular Disorders Research
  • RNA regulation and disease
  • Heparin-Induced Thrombocytopenia and Thrombosis
  • Blood Coagulation and Thrombosis Mechanisms
  • Restraint-Related Deaths
  • Protein Degradation and Inhibitors

Regen BioPharma (United States)
 2015

Columbia University
 2014

 Effect of the REG1 anticoagulation system versus bivalirudin on outcomes after percutaneous coronary intervention (REGULATE-PCI): a randomised clinical trial
OPENALEX - Publications 
A. Michael Lincoff Roxana Mehran Thomas J. Povsic Steven L. Zelenkofske Zhen Huang and 28 more Paul W. Armstrong Philippe Gabríel Steg Christoph Bode Mauricio G. Cohen Christopher E. Buller Peep Laanmets Marco Valgimigli Toomas Marandi Viliam Fridrich Warren J. Cantor Béla Merkely José López‐Sendón Jan H. Cornel Jarosław D. Kasprzak Michael Aschermann Victor Guetta João Morais Peter Sinnaeve Kurt Huber Rod Stables Mary Ann Sellers Marilyn Borgman Lauren Glenn Arnold I. Levinson Renato D. Lópes Vic Hasselblad Richard C. Becker John H. Alexander

10.1016/s0140-6736(15)00515-2 article EN The Lancet 2015-11-05
 Feasibility of at-home motor assessments using wireless technology in patients with myelopathy: year 1 follow up of CYGNET, an observational study of patients with adrenomyeloneuropathy (P6-6.006)
OPENALEX - Publications 
Caroline Bergner Wolfgang Köehler Joshua L. Bonkowsky Christopher D. Stephen Asif Paker and 4 more Florian Eichler Lauren Glenn Steven L. Zelenkofske Marc Engelen

<h3>Objective:</h3> To quantify change in symptoms over time using home-based gait and mobility assessments from a prospective natural history study of patients with adrenomyeloneuropathy (AMN). <h3>Background:</h3> AMN is rare neurodegenerative disorder the brain spinal cord affecting adults mutations <i>ABCD1</i> gene. Quantification disease progression challenging, owing to phenotypic variability. One solution address this measure traditional functional motor tasks more frequently...

10.1212/wnl.0000000000201912 article EN Neurology 2023-04-25
Coming Soon ...