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Movement Disorders : Official Journal of the Movement Disorder Society|June 29, 2019
Evolution and clustering of prodromal parkinsonian features in GBA1 carriersStephen Mullin, Michelle Beavan, Jonathan Bestwick, et al.
Annals of the American Thoracic Society|April 21, 2016
Rapid On-Site Evaluation in Detection of Granulomas in the Mediastinal Lymph NodesHaala K Rokadia, Atul Mehta, Daniel A Culver, et al.
Chest|January 25, 2020
Association Between Inhaled Corticosteroids and TracheobronchomalaciaVarun Shah, Bryan Husta, Atul Mehta, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 5, 2020
Brain Microglial Activation Increased in Glucocerebrosidase (GBA) Mutation Carriers without Parkinson's diseaseStephen Mullin, Morten Gersel Stokholm, Derralyn Hughes, et al.
Clinical Neurology and Neurosurgery|May 19, 2007
Middelheim Fabry Study (MiFaS): a retrospective Belgian study on the prevalence of Fabry disease in young patients with cryptogenic strokeRaf Brouns, Rishi Sheorajpanday, Ellen Braxel, et al.
Transplantation Proceedings|August 31, 2024
Kaposi Sarcoma in Two Lung Transplant Recipients: A Single-Center ExperienceAvantika Nathani, Jessica Lum, Shruti Gadre, et al.
The Journal of Obstetrics and Gynaecology Research|March 12, 2014
Outcome of pregnancies in women receiving velaglucerase alfa for Gaucher diseaseDeborah Elstein, Derralynn Hughes, Ozlem Goker-Alpan, et al.
Blood Cells, Molecules & Diseases|May 21, 2013
Miglustat therapy in type 1 Gaucher disease: clinical and safety outcomes in a multicenter retrospective cohort studyDavid J Kuter, Atul Mehta, Carla E M Hollak, et al.
Journal of the American Society of Nephrology : JASN|April 10, 2009
Agalsidase alfa and kidney dysfunction in Fabry diseaseMichael West, Kathy Nicholls, Atul Mehta, et al.
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