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Journal of Virology|March 22, 2013
Immunological hallmarks of JC virus replication in multiple sclerosis patients on long-term natalizumab therapyHouria Hendel-Chavez, Marie-Ghislaine de Goër de Herve, Claire Giannesini, et al.
Neurology|October 22, 2020
Neurofilament Light Chain as a Biomarker of Hereditary Transthyretin-Mediated AmyloidosisSimina Ticau, Gautham V Sridharan, Shira Tsour, et al.
The Journal of Thoracic and Cardiovascular Surgery|November 29, 2015
Prosthesis-patient mismatch in high-risk patients with severe aortic stenosis: A randomized trial of a self-expanding prosthesisGeorge L Zorn, Stephen H Little, Peter Tadros, et al.
Translational Research : the Journal of Laboratory and Clinical Medicine|November 14, 2018
Glycomics in rare diseases: from diagnosis tomechanismMariska Davids, Megan S Kane, Lynne A Wolfe, et al.
Heart Rhythm|February 15, 2015
Using skin sympathetic nerve activity to estimate stellate ganglion nerve activity in dogsZhaolei Jiang, Ye Zhao, Anisiia Doytchinova, et al.
Cell Transplantation|April 25, 2024
Alpha-1 Antitrypsin Augmentation Therapy in Chronic Pancreatitis Patients Undergoing Total Pancreatectomy and Islet Autotransplantation: A Randomized, Controlled StudyHongjun Wang, Wenyu Gou, Paul J Nietert, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 15, 2010
Speech disturbances in patients with dystonia or chorea due to neurometabolic disordersConstance Flamand-Rouvière, Emilie Guettard, Caroline Moreau, et al.
Heart Rhythm|August 6, 2017
Left cervical vagal nerve stimulation reduces skin sympathetic nerve activity in patients with drug resistant epilepsyYuan Yuan, Jonathan L Hassel, Anisiia Doytchinova, et al.
Investigative Ophthalmology & Visual Science|April 9, 2011
Genetic heterogeneity for recessively inherited congenital cataract microcornea with corneal opacityKamron Khan, Ahmed Al-Maskari, Martin McKibbin, et al.
Orphanet Journal of Rare Diseases|July 10, 2020
A phase II, open-label, extension study of long-term patisiran treatment in patients with hereditary transthyretin-mediated (hATTR) amyloidosisTeresa Coelho, David Adams, Isabel Conceição, et al.
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