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NPJ Genomic Medicine|August 23, 2018
Two different STAT1 gain-of-function mutations lead to diverse IFN-γ-mediated gene expressionAdi Ovadia, Nigel Sharfe, Cynthia Hawkins, et al.
Microcirculation (New York, N.Y. : 1994)|September 16, 2014
Adaptations of the endothelin system after exercise training in a porcine model of ischemic heart diseaseJuan Carlos Robles, Cristine L Heaps
Acta Gastroenterologica Latinoamericana|December 4, 2025
[Endoscopic Anti-Reflux Therapy for Gastroesophageal Reflux Disease: A Present-Day Perspective]Juan Ignacio Olmos, Carlos Robles-Medranda
Journal of Clinical Imaging Science|May 5, 2022
T1 hyperintensity in the spinal cord: A diagnostic marker of amyotrophic lateral sclerosis?Vivek Pai, Chintan R Trivedi, Bhujang Pai, et al.
Neuro-Oncology|May 26, 2006
Diffusion tensor imaging of white matter after cranial radiation in children for medulloblastoma: correlation with IQDonald J Mabbott, Michael D Noseworthy, Eric Bouffet, et al.
American Journal of Medical Genetics. Part A|February 18, 2017
Homozygous mutation in PRUNE1 in an Oji-Cree male with a complex neurological phenotypeGregory Costain, Andrea Shugar, Pradeep Krishnan, et al.
BMJ Case Reports|December 1, 2020
Acute subdural haemorrhage complicating cerebral venous thrombosis in a patient with protein C deficiencyElvin Yuan Ting Lim, Vivek Pai, Yih Yian Sitoh, et al.
Insights Into Imaging|November 12, 2021
Rhino-orbito-cerebral Mucormycosis: Pictorial ReviewVivek Pai, Rima Sansi, Ritesh Kharche, et al.
AJNR. American Journal of Neuroradiology|May 14, 2005
Nocardial endophthalmitis and subretinal abscess: CT and MR imaging features with pathologic correlation: a case reportEugene Yu, Suzanne Laughlin, Edward E Kassel, et al.
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