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International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society|July 6, 2018
Efficacy of Hyperthermic Intraperitoneal Chemotherapy and Cytoreductive Surgery in the Treatment of Recurrent Uterine SarcomaTeresa P Díaz-Montes, Farah El-Sharkawy, Sarah Lynam, et al.
Frontiers in Oncology|June 1, 2026
Poly(ADP-ribose) polymerase inhibitor maintenance therapy in ovarian cancer: a single-center retrospective studySydney Pence, Kayla Dyson, Kristen Waters, et al.
American Journal of Medical Genetics. Part A|March 10, 2016
Autosomal recessive MFN2-related Charcot-Marie-Tooth disease with diaphragmatic weakness: Case report and literature reviewChristopher A Tan, Marina Rabideau, Amy Blevins, et al.
Radiology Case Reports|March 18, 2021
Aggressive vertebral hemangioma masquerading as neurological disease in a pediatric patientDivya Sahajwalla, Gregory Vorona, Gary Tye, et al.
Seizure|February 22, 2011
Successful ECT treatment for medically refractory nonconvulsive status epilepticus in pediatric patientHae W Shin, Cormac A O'Donovan, Jane G Boggs, et al.
Brain Communications|October 30, 2025
Task-based effective connectivity finds alterations in frontoparietal network in Duchenne muscular dystrophyMathula Thangarajh, Matthew Ridder, Hakinya Karra, et al.
Annals of Clinical and Translational Neurology|February 16, 2022
TRPV4 mutations causing mixed neuropathy and skeletal phenotypes result in severe gain of functionArens Taga, Margo A Peyton, Benedikt Goretzki, et al.
Annals of Neurology|July 28, 2016
KIF5A mutations cause an infantile onset phenotype including severe myoclonus with evidence of mitochondrial dysfunctionJessica Duis, Shannon Dean, Carolyn Applegate, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|December 28, 2018
Anti-HMGCR myopathy may resemble limb-girdle muscular dystrophyPayam Mohassel, Océane Landon-Cardinal, A Reghan Foley, et al.
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