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Clinical Neuropathology|August 23, 2016
Clinical Neuropathology image 5-2016: nNeurofibrillary tangle-rich gangliogliomaEllen Gelpi, Romana Höftberger, Tanja Würger, et al.Clinical Neuropathology|May 30, 2018
Cerebellar high-grade gliomas do not present the same molecular alterations as supratentorial high-grade gliomas and may show histone H3 gene mutationsArnault Tauziède-Espariat, Raphaël Saffroy, Mélanie Pagès, et al.Clinical Neuropathology|May 28, 2019
ALDH1 - A new immunohistochemical diagnostic marker for Schwann cell-derived tumorsFriederike Liesche, Michael Griessmair, Melanie Barz, et al.Clinical Neuropathology|December 20, 2019
How frequent is double pathology in Rasmussen encephalitis?Ahmed Gilani, Bette K Kleinschmidt-DeMastersClinical Neuropathology|May 16, 2022
Life and death of molecular subclones in recurrent meningioma: A case studyNiklas Abele, Elmar Kirches, I Erol Sandalcioglu, et al.Clinical Neuropathology|June 2, 2022
DNAJB2 c.184C>T mutation associated with distal hereditary motor neuropathy with rimmed vacuolar myopathyMeige Liu, Yan Xu, Daojun Hong, et al.Clinical Neuropathology|March 1, 1987
A morphometric reevaluation of Huntington's chorea with special reference to the large neurons in the neostriatumK Oyanagi, F IkutaClinical Neuropathology|June 7, 2022
Diagnostic DNA methylome profiling and the WHO 5th edition CNS tumor classificationStephan Frank, Jürgen HenchClinical Neuropathology|May 23, 2022
A novel compound heterozygous mutation in the COA7 gene responsible for a Chinese patient with spinocerebellar ataxia with axonal neuropathy type 3Yuwei Tang, Meng Yu, Wei Zhang, et al.Clinical Neuropathology|June 30, 2022
H3 K27M-mutant diffuse midline glioma with osseous metastases: A case report and a literature reviewSarah Al Sharie, Muna Talafha, Dima Abu Laban, et al.Pageof 165