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Cancer Medicine|October 30, 2024
Measuring the diagnostic management and follow-up imaging for glioma patients across Belgian hospitals between 2016 and 2019Dimitri Vanhauwaert, Katrijn Vanschoenbeek, Frank Weyns, et al.
BMC Medical Genetics|May 21, 2017
Pancreas and gallbladder agenesis in a newborn with semilobar holoprosencephaly, a case reportRobert Hilbrands, Kathelijn Keymolen, Alex Michotte, et al.
Anatomical Record (Hoboken, N.J. : 2007)|February 19, 2017
Comparison of Several White Matter Tracts in Feline and Canine Brain by Using Magnetic Resonance Diffusion Tensor ImagingOlivier Jacqmot, Bert Van Thielen, Alex Michotte, et al.
Acta Neurologica Belgica|September 18, 2008
Management of diffuse glioma in children: a retrospective study of 27 cases and review of literatureCaroline Piette, Manuel Deprez, Jacques Born, et al.
Anticancer Research|December 27, 2011
Correlation between IDH1 gene mutation status and survival of patients treated for recurrent gliomaShasha Lv, Erik Teugels, Jan Sadones, et al.
The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry|September 9, 2017
Slc7a11 (xCT) protein expression is not altered in the depressed brain and system xc- deficiency does not affect depression-associated behaviour in the corticosterone mouse modelThomas Demuyser, Lauren Deneyer, Eduard Bentea, et al.
Case Reports in Oncological Medicine|August 9, 2014
Symptomatic Histologically Proven Necrosis of Brain following Stereotactic Radiation and Ipilimumab in Six Lesions in Four Melanoma PatientsStephanie Du Four, Angela Hong, Matthew Chan, et al.
Journal for Immunotherapy of Cancer|October 17, 2020
Axitinib plus avelumab in the treatment of recurrent glioblastoma: a stratified, open-label, single-center phase 2 clinical trial (GliAvAx)Gil Awada, Laila Ben Salama, Jennifer De Cremer, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|April 29, 2015
Evidence-Based Diagnostic Algorithm for Glioma: Analysis of the Results of Pathology Panel Review and Molecular Parameters of EORTC 26951 and 26882 TrialsJohan M Kros, Karin Huizer, Aurelio Hernández-Laín, et al.
Human Mutation|November 12, 2014
Two siblings with homozygous pathogenic splice-site variant in mitochondrial asparaginyl-tRNA synthetase (NARS2)Arnaud V Vanlander, Björn Menten, Joél Smet, et al.
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