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Familial Creutzfeldt–Jakob disease homozygous to the E200K mutation: clinical characteristics and disease course

Journal of neurology, 2020-08, Vol.267 (8), p.2455-2458

2020

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Increased in vivo expression of an inflammatory marker in temporal lobe epilepsy

Journal of Nuclear Medicine, 2012-02, Vol.53 (2), p.234-240

2012

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Efficacy of Head Repositioning in Restoration of Electrophysiological Signals During Cervical Spine Procedures

Journal of clinical neurophysiology, 2017-03, Vol.34 (2), p.174-178

2017

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Intraoperative monitoring of corticospinal tracts in anterior cervical decompression and fusion surgery: Excitability differentials of lower extremity muscles

Clinical neurophysiology practice, 2020-01, Vol.5, p.59-63

2020

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The EEG in E200K familial CJD: relation to MRI patterns

Journal of neurology, 2012-03, Vol.259 (3), p.491-496

2012

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Serum calcium levels and long-term mortality in patients with acute stroke

Cerebrovascular diseases (Basel, Switzerland), 2011-01, Vol.31 (1), p.93-9

2011

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Infection and vaccination in chronic fatigue syndrome: Myth or reality?

Autoimmunity (Chur, Switzerland), 2007-01, Vol.40 (1), p.48-53

2007

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Effect of Intra- and Extraoperative Factors on the Efficacy of Intraoperative Neuromonitoring During Cervical Spine Surgery

World neurosurgery, 2019-03, Vol.123, p.e646-e651

2019

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Intraoperative Deterioration of Neurophysiological Potentials of the Spinal Tracts in Cervical Spine Surgery: Correlation With Patient-Related and Procedure-Related Variables

Journal of clinical neurophysiology, 2023-05, Vol.40 (4), p.325-330

2023

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Sensory disturbances in Creutzfeldt-Jakob disease

Neurological sciences, 2024-03, Vol.45 (3), p.1057-1062

2024

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Progressive multifocal leukoencephalopathy in a patient with chronic lymphocytic leukemia after immunosuppressive treatment

Neurology and clinical neuroscience, 2017-01, Vol.5 (1), p.29-31

2017

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Spinal intradural extramedullary tumors: the value of intraoperative neurophysiologic monitoring on surgical outcome

Neurosurgical review, 2017-10, Vol.40 (4), p.613-619

2017

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The epidemiological and clinical characteristics of patients with young-onset genetic Creutzfeldt-Jakob disease

Neurological research (New York), 2023-09, Vol.ahead-of-print (ahead-of-print), p.1-4

2023

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Genetic Creutzfeldt‐Jakob disease in Turkish Jews—demographic and clinical features

Acta neurologica Scandinavica, 2022-11, Vol.146 (5), p.586-589

2022

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Epidemiological and clinical characteristics of patients with late-onset Creutzfeldt-Jakob disease

Neurological sciences, 2022-07, Vol.43 (7), p.4275-4279

2022

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A retrospective analysis of the development of seizure frequency in patients with seizures during a period of military conflict

Seizure (London, England), 2018-10, Vol.61, p.119-121

2018

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The consequences of switching from Gilenya® to generics for fingolimod

Multiple sclerosis and related disorders, 2023-06, Vol.74, p.104692-104692, Article 104692

2023

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The association of quantitative EEG and MRI in Creutzfeldt‐Jakob Disease

Acta neurologica Scandinavica, 2019-11, Vol.140 (5), p.366-371

2019

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Mycosis fungoides – A cutaneous lymphoproliferative disorder in a patient treated with fingolimod for multiple sclerosis

Journal of clinical neuroscience, 2018-02, Vol.48, p.102-103

2018

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Association between cervical disc disease and lesions of multiple sclerosis

The neuroradiology journal, 2021-06, Vol.34 (3), p.200-204

2021

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Spatial distribution of abnormal EEG activity in Creutzfeldt-Jakob disease

Neurophysiologie clinique, 2021-06, Vol.51 (3), p.219-224

2021

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Disease duration in E200K familial Creutzfeldt–Jakob disease is correlated with clinical, radiological, and laboratory variables

Journal of Neural Transmission, 2019-05, Vol.126 (5), p.607-611

2019

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Familial Creutzfeldt–Jakob disease with the E200K mutation: longitudinal neuroimaging from asymptomatic to symptomatic CJD

Journal of neurology, 2015-03, Vol.262 (3), p.604-613

2015

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Serotonin 1A receptors, depression, and memory in temporal lobe epilepsy

Epilepsia (Copenhagen), 2012-01, Vol.53 (1), p.129-133

2012

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Unusual presentations in patients with E200K familial Creutzfeldt−Jakob disease

European journal of neurology, 2016-05, Vol.23 (5), p.871-877

2016

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Familial Creutzfeldt–Jakob disease homozygous to the E200K mutation: clinical characteristics and disease course

Increased in vivo expression of an inflammatory marker in temporal lobe epilepsy

Efficacy of Head Repositioning in Restoration of Electrophysiological Signals During Cervical Spine Procedures

Intraoperative monitoring of corticospinal tracts in anterior cervical decompression and fusion surgery: Excitability differentials of lower extremity muscles

The EEG in E200K familial CJD: relation to MRI patterns

Serum calcium levels and long-term mortality in patients with acute stroke

Infection and vaccination in chronic fatigue syndrome: Myth or reality?

Effect of Intra- and Extraoperative Factors on the Efficacy of Intraoperative Neuromonitoring During Cervical Spine Surgery

Intraoperative Deterioration of Neurophysiological Potentials of the Spinal Tracts in Cervical Spine Surgery: Correlation With Patient-Related and Procedure-Related Variables

Sensory disturbances in Creutzfeldt-Jakob disease

Progressive multifocal leukoencephalopathy in a patient with chronic lymphocytic leukemia after immunosuppressive treatment

Spinal intradural extramedullary tumors: the value of intraoperative neurophysiologic monitoring on surgical outcome

The epidemiological and clinical characteristics of patients with young-onset genetic Creutzfeldt-Jakob disease

Genetic Creutzfeldt‐Jakob disease in Turkish Jews—demographic and clinical features

Epidemiological and clinical characteristics of patients with late-onset Creutzfeldt-Jakob disease

A retrospective analysis of the development of seizure frequency in patients with seizures during a period of military conflict

The consequences of switching from Gilenya® to generics for fingolimod

The association of quantitative EEG and MRI in Creutzfeldt‐Jakob Disease

Mycosis fungoides – A cutaneous lymphoproliferative disorder in a patient treated with fingolimod for multiple sclerosis

Association between cervical disc disease and lesions of multiple sclerosis

Spatial distribution of abnormal EEG activity in Creutzfeldt-Jakob disease

Disease duration in E200K familial Creutzfeldt–Jakob disease is correlated with clinical, radiological, and laboratory variables

Familial Creutzfeldt–Jakob disease with the E200K mutation: longitudinal neuroimaging from asymptomatic to symptomatic CJD

Serotonin 1A receptors, depression, and memory in temporal lobe epilepsy

Unusual presentations in patients with E200K familial Creutzfeldt−Jakob disease

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