Showing results (741-750 of 841) with videos related to

Sort By:
Pageof 85
Contemporary Clinical Trials Communications|August 4, 2023
C-STIM: Protocol for a randomized, single-blind, crossover study of cerebellar repetitive transcranial magnetic stimulation (rTMS) for postural instability in people with progressive supranuclear palsy (PSP)M L Dale, M Mancini, A Stevens, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|March 31, 2012
Hepatic dysfunction and survival after orthotopic heart transplantation: application of the MELD scoring system for outcome predictionAalap Chokshi, Faisal H Cheema, Kenneth J Schaefle, et al.
Leukemia|March 17, 2000
Use of dual-color interphase FISH for the detection of inv(16) in acute myeloid leukemia at diagnosis, relapse and during follow-up: a study of 23 patientsM Mancini, M Cedrone, D Diverio, et al.
Annals of Hematology|July 2, 2003
High-dose hydroxyurea in the treatment of poor-risk myeloid leukemiasM C Petti, A Tafuri, R Latagliata, et al.
Circulation. Heart Failure|September 15, 2016
Recovery of Serum Cholesterol Predicts Survival After Left Ventricular Assist Device ImplantationAmanda R Vest, Peter J Kennel, Dawn Maldonado, et al.
Atherosclerosis|August 5, 2000
Intima-media thickness after pravastatin stabilizes also in patients with moderate to no reduction in LDL-cholesterol levels: the carotid atherosclerosis Italian ultrasound studyD Baldassarre, F Veglia, C Gobbi, et al.
Circulation|November 24, 1999
Outcome after orthotopic cardiac transplantation in adults with congenital heart diseaseJ M Lamour, L J Addonizio, M E Galantowicz, et al.
JAMA Cardiology|April 16, 2020
Strategies of Wait-listing for Heart Transplant vs Durable Mechanical Circulatory Support Alone for Patients With Advanced Heart FailureAnuradha Lala, John C Rowland, Bart S Ferket, et al.
Nature Genetics|December 2, 1999
A new gene, encoding an anion transporter, is mutated in sialic acid storage diseasesF W Verheijen, E Verbeek, N Aula, et al.
Molecular Endocrinology (Baltimore, Md.)|December 22, 1999
A C619Y mutation in the human androgen receptor causes inactivation and mislocalization of the receptor with concomitant sequestration of SRC-1 (steroid receptor coactivator 1)L V Nazareth, D L Stenoien, W E Bingman, et al.
Pageof 85