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Robert Rusina

Showing results (21-30 of 40) with videos related to

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Clinical Rheumatology|December 3, 2005
Combined CNS and pituitary involvement as a primary manifestation of Wegener granulomatosisRadek Spísek, Elena Kolouchová, Jirí Jensovský, et al.
Clinical EEG and Neuroscience|October 18, 2013
Change in the characteristics of EEG color noise in Alzheimer's diseaseOldrich Vysata, Ales Procházka, Jan Mares, et al.
Neurologia I Neurochirurgia Polska|February 26, 2017
The Heidenhain variant of Creutzfeldt-Jakob disease and concomitant tau pathology: A case reportEdvard Ehler, Michael Pipka, Alena Meleková, et al.
Plos One|August 31, 2013
New non-linear color look-up table for visualization of brain fractional anisotropy based on normative measurements - principals and first clinical useJiří Keller, Aaron M Rulseh, Arnošt Komárek, et al.
Cerebellum & Ataxias|August 5, 2017
Cognitive impairment in cerebellar lesions: a logit model based on neuropsychological testingEva Bolceková, Matej Mojzeš, Quang Van Tran, et al.
Frontiers in Neurology|December 17, 2020
Sporadic Creutzfeldt-Jakob Disease and Other Proteinopathies in ComorbidityEva Parobkova, Julie van der Zee, Lubina Dillen, et al.
Experimental Neurology|June 19, 2010
Increased neuronal Rab5 immunoreactive endosomes do not colocalize with TDP-43 in motor neuron diseaseRadoslav Matej, Gergö Botond, Lajos László, et al.
Neurocase|April 13, 2012
Gerstmann-Sträussler-Scheinker syndrome with the P102L pathogenic mutation presenting as familial Creutzfeldt-Jakob disease: a case report and review of the literatureRobert Rusina, Jindřich Fiala, Karel Holada, et al.
Biomedicines|March 25, 2022
Biomarkers Analysis and Clinical Manifestations in Comorbid Creutzfeldt-Jakob Disease: A Retrospective Study in 215 Autopsy CasesNikol Jankovska, Robert Rusina, Jiri Keller, et al.
BMC Neurology|May 17, 2011
FTLD-TDP with motor neuron disease, visuospatial impairment and a progressive supranuclear palsy-like syndrome: broadening the clinical phenotype of TDP-43 proteinopathies. A report of three casesRobert Rusina, Gabor G Kovacs, Jindřich Fiala, et al.
Pageof 4

Showing results (21-30 of 40) with videos related to

Sort By:
Pageof 4
Clinical Rheumatology|December 3, 2005
Combined CNS and pituitary involvement as a primary manifestation of Wegener granulomatosisRadek Spísek, Elena Kolouchová, Jirí Jensovský, et al.
Clinical EEG and Neuroscience|October 18, 2013
Change in the characteristics of EEG color noise in Alzheimer's diseaseOldrich Vysata, Ales Procházka, Jan Mares, et al.
Neurologia I Neurochirurgia Polska|February 26, 2017
The Heidenhain variant of Creutzfeldt-Jakob disease and concomitant tau pathology: A case reportEdvard Ehler, Michael Pipka, Alena Meleková, et al.
Plos One|August 31, 2013
New non-linear color look-up table for visualization of brain fractional anisotropy based on normative measurements - principals and first clinical useJiří Keller, Aaron M Rulseh, Arnošt Komárek, et al.
Cerebellum & Ataxias|August 5, 2017
Cognitive impairment in cerebellar lesions: a logit model based on neuropsychological testingEva Bolceková, Matej Mojzeš, Quang Van Tran, et al.
Frontiers in Neurology|December 17, 2020
Sporadic Creutzfeldt-Jakob Disease and Other Proteinopathies in ComorbidityEva Parobkova, Julie van der Zee, Lubina Dillen, et al.
Experimental Neurology|June 19, 2010
Increased neuronal Rab5 immunoreactive endosomes do not colocalize with TDP-43 in motor neuron diseaseRadoslav Matej, Gergö Botond, Lajos László, et al.
Neurocase|April 13, 2012
Gerstmann-Sträussler-Scheinker syndrome with the P102L pathogenic mutation presenting as familial Creutzfeldt-Jakob disease: a case report and review of the literatureRobert Rusina, Jindřich Fiala, Karel Holada, et al.
Biomedicines|March 25, 2022
Biomarkers Analysis and Clinical Manifestations in Comorbid Creutzfeldt-Jakob Disease: A Retrospective Study in 215 Autopsy CasesNikol Jankovska, Robert Rusina, Jiri Keller, et al.
BMC Neurology|May 17, 2011
FTLD-TDP with motor neuron disease, visuospatial impairment and a progressive supranuclear palsy-like syndrome: broadening the clinical phenotype of TDP-43 proteinopathies. A report of three casesRobert Rusina, Gabor G Kovacs, Jindřich Fiala, et al.
Pageof 4