Showing results (61-70 of 90) with videos related to

Sort By:
Pageof 9
Neuro-Oncology|October 26, 2013
Primary glioblastoma with oligodendroglial differentiation has better clinical outcome but no difference in common biological markers compared with other types of glioblastomaRoss C Laxton, Sergey Popov, Lawrence Doey, et al.
Seizure|July 23, 2013
Preoperative estimation of seizure control after resective surgery for the treatment of epilepsyAtul Kumar, Antonio Valentín, Danish Humayon, et al.
Acta Neurochirurgica|March 17, 2023
H3 G34-mutant high-grade gliomas: integrated clinical, imaging and pathological characterisation of a single-centre case seriesJosé Pedro Lavrador, Zita Reisz, Naomi Sibtain, et al.
Pathology Oncology Research : POR|May 20, 2026
Case Report: The molecular profile of granular cell astrocytoma predicts aggressive clinical behavior, independent of morphologyMelanie Jensen, Pranoy Das, Oliver Wroe-Wright, et al.
American Journal of Medical Genetics. Part A|February 27, 2010
Vici syndrome associated with sensorineural hearing loss and evidence of neuromuscular involvement on muscle biopsyVerity McClelland, Thomas Cullup, Istvan Bodi, et al.
Pain|June 29, 2014
Sensory, psychological, and metabolic dysfunction in HIV-associated peripheral neuropathy: A cross-sectional deep profiling studyTudor J C Phillips, Matthew Brown, Juan D Ramirez, et al.
Pediatric Hematology and Oncology|April 26, 2021
High grade gliomas in young children: The South Thames Neuro-Oncology unit experience and recent advances in molecular biology and targeted therapiesJanice Pearce, Komel Khabra, Henry Nanji, et al.
Journal of Inherited Metabolic Disease|March 19, 2020
RBCK1-related disease: A rare multisystem disorder with polyglucosan storage, auto-inflammation, recurrent infections, skeletal, and cardiac myopathy-Four additional patients and a review of the current literatureRahul Phadke, Carola Hedberg-Oldfors, Renata S Scalco, et al.
Neuromolecular Medicine|January 8, 2013
Novel mutations mapping to the fourth sodium channel domain of Nav1.7 result in variable clinical manifestations of primary erythromelalgiaRoman Cregg, Bisola Laguda, Robert Werdehausen, et al.
Acta Neuropathologica Communications|January 15, 2025
An exceptionally rare case of a diffuse midline glioma with concomitant H3.1 K27M and G34R mutations in the HIST1H3C (H3C3) geneZita Reisz, Rita Pereira, Smitha Nevis, et al.
Pageof 9