Showing results (11-20 of 24) with videos related to
Sort By:
Pageof 3
Journal of Magnetic Resonance Imaging : JMRI|March 3, 2004
Usefulness of contrast kinetics for predicting and monitoring tissue changes in muscle following thermal therapy in long survival studiesHai-Ling Margaret Cheng, Carrie M Purcell, Juan M Bilbao, et al.Journal of Magnetic Resonance Imaging : JMRI|October 28, 2003
Prediction of subtle thermal histopathological change using a novel analysis of Gd-DTPA kineticsHai-Ling Margaret Cheng, Carrie M Purcell, Juan M Bilbao, et al.Endocrine Pathology|July 13, 2002
Xanthomatous Hypophysitis: A Novel Entity of Obscure EtiologySanjeev S. Deodhare, Juan M. Bilbao, Kalman Kovacs, et al.Skull Base : Official Journal of North American Skull Base Society ... [Et Al.]|February 15, 2011
Aspergillosis of the Petrous Apex and Meckel's CaveAsh Ederies, Joseph Chen, Richard I Aviv, et al.The Laryngoscope|June 10, 2009
Chondromyxoid fibroma of the mastoid facial nerve canal mimicking a facial nerve schwannomaAndrew L Thompson, Aditya Bharatha, Richard I Aviv, et al.Pathology, Research and Practice|May 28, 2015
Diagnostic and prognostic biomarkers of a sellar melanocytic tumor mimicking pituitary adenoma: Case report and literature reviewAmeen A Mohammed, Fabio Rotondo, David G Munoz, et al.BMC Neurology|March 22, 2013
Exome sequencing identifies titin mutations causing hereditary myopathy with early respiratory failure (HMERF) in families of diverse ethnic originsCamilo Toro, Montse Olivé, Marinos C Dalakas, et al.Lasers in Surgery and Medicine|September 25, 2004
Increased brain tumor resection using fluorescence image guidance in a preclinical modelArjen Bogaards, Abhay Varma, Sean P Collens, et al.Journal of Alzheimer'S Disease : JAD|October 9, 2010
Intra-familial clinical heterogeneity due to FTLD-U with TDP-43 proteinopathy caused by a novel deletion in progranulin gene (PGRN)Tomasz Gabryelewicz, Mario Masellis, Mariusz Berdynski, et al.Acta Neuropathologica|July 31, 2012
Transportin 1 accumulates specifically with FET proteins but no other transportin cargos in FTLD-FUS and is absent in FUS inclusions in ALS with FUS mutationsManuela Neumann, Chiara F Valori, Olaf Ansorge, et al.Pageof 3