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Neurogenetics|May 27, 2005
Identification of a VPS13A founder mutation in French Canadian families with chorea-acanthocytosisCarol Dobson-Stone, Antonio Velayos-Baeza, An Jansen, et al.
Human Molecular Genetics|April 6, 2007
Triplet repeat mutation length gains correlate with cell-type specific vulnerability in Huntington disease brainPeggy F Shelbourne, Christine Keller-McGandy, Wenya Linda Bi, et al.
Journal of the National Cancer Institute|April 17, 1996
Potential role of the inactivated X chromosome in ovarian epithelial tumor developmentP C Cheng, J A Gosewehr, T M Kim, et al.
Annals of Neurology|November 14, 2022
A Subpopulation of Spikes Predicts Successful Epilepsy Surgery OutcomeJohn Thomas, Philippe Kahane, Chifaou Abdallah, et al.
British Journal of Haematology|July 30, 2016
Renal disease related to Waldenström macroglobulinaemia: incidence, pathology and clinical outcomesJosephine M Vos, Joshua Gustine, Helmut G Rennke, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|October 3, 2022
"Generalized-to-focal" epilepsy: stereotactic EEG and high-frequency oscillation patternsNicolas von Ellenrieder, Francois Dubeau, Roy W. R. Dudley, et al.
Oncogene|May 1, 2021
Endoplasmic reticulum chaperone GRP78/BiP is critical for mutant Kras-driven lung tumorigenesisDaisy Flores Rangel, Louis Dubeau, Ryan Park, et al.
Epilepsia|August 18, 2023
Interictal high-frequency oscillations, spikes, and connectivity profiles: A fingerprint of epileptogenic brain pathologiesBarbora Sklenarova, Eva Zatloukalova, Jan Cimbalnik, et al.
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