Showing results (21-30 of 37) with videos related to

Sort By:
Pageof 4
Neuromuscular Disorders : NMD|February 9, 2021
Homozygous intronic variants in TPM2 cause recessively inherited Escobar variant of multiple pterygium syndrome and congenital myopathySchaida Schirwani, Anna Sarkozy, Rahul Phadke, et al.
Acta Neuropathologica|August 21, 2018
Estimation of amyloid distribution by [18F]flutemetamol PET predicts the neuropathological phase of amyloid β-protein depositionDietmar Rudolf Thal, Thomas G Beach, Michelle Zanette, et al.
Frontiers in Oncology|April 2, 2019
FGFR1 Expression and Role in Migration in Low and High Grade Pediatric GliomasNaomi Egbivwie, Julia V Cockle, Matthew Humphries, et al.
Muscle & Nerve|August 1, 2009
A RYR1 mutation associated with recessive congenital myopathy and dominant malignant hyperthermia in Asian familiesDanielle Carpenter, Azzam Ismail, Rachel L Robinson, et al.
World Neurosurgery|November 14, 2017
Low-Grade Glioma with Foci of Early Transformation Does Not Necessarily Require Adjuvant Therapy After Radical Surgical ResectionYahia Zaki Al-Tamimi, Martin S Palin, Tufail Patankar, et al.
International Journal of Cancer|December 2, 2017
How to analyse the spatiotemporal tumour samples needed to investigate cancer evolution: A case study using paired primary and recurrent glioblastomaAlastair Droop, Alexander Bruns, Georgette Tanner, et al.
Neuro-Oncology|September 3, 2025
Spatial profiling of longitudinal glioblastoma reveals consistent changes in cellular architecture, post-treatmentShoaib Ajaib, Joshua Winter-Luke, Richard J Digby, et al.
Acta Neuropathologica Communications|December 14, 2016
Post-mortem histopathology underlying β-amyloid PET imaging following flutemetamol F 18 injectionMilos D Ikonomovic, Chris J Buckley, Kerstin Heurling, et al.
Pageof 4