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Prevalence of carpal tunnel syndrome and its correlation with pain amongst female hairdressers

International journal of occupational medicine and environmental health, 2018-01, Vol.31 (3), p.333-339

2018

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Quantitative phase imaging of erythrocyte in epilepsy patients

Microscopy research and technique, 2021-06, Vol.84 (6), p.1172-1180

2021

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The effect of pelvic floor exercise program on incontinence and sexual dysfunction in multiple sclerosis patients

International urology and nephrology, 2021-06, Vol.53 (6), p.1059-1065

2021

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The Frequency of Fabry Disease among Young Cryptogenic Stroke Patients in the City of Sakarya

Journal of stroke and cerebrovascular diseases, 2017-06, Vol.26 (6), p.1334-1340

2017

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Clinical and molecular characterization and response to acitretin in three families with Sjögren‐Larsson syndrome

International journal of dermatology, 2018-07, Vol.57 (7), p.843-848

2018

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SCN1A GENE SEQUENCING IN 46 TURKISH EPILEPSY PATIENTS DISCLOSED 12 NOVEL MUTATIONS

Seizure (London, England), 2016-07, Vol.39, p.34-43

2016

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Predictors of intensive care unit admission and mortality in patients with ischemic stroke: investigating the effects of a pulmonary rehabilitation program

BMC neurology, 2017-07, Vol.17 (1), p.132-132, Article 132

2017

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Diaphragm pacing system implanted in a patient with ALS

Journal of back and musculoskeletal rehabilitation, 2016-08, Vol.29 (3), p.611-612

2016

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The Evaluation of Botulinum Toxin Injection Effect for Poststroke Spasticity Treatment

Türk nöroloji dergisi, 2017-03, Vol.23 (1), p.15-20

2017

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The effect of cognitive performance on self-management behavior of multiple sclerosis patients

Multiple sclerosis and related disorders, 2022-07, Vol.63, p.103880-103880, Article 103880

2022

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Autosomal Recessive Parkinson’s Disease with Early-Onset in a Turkish Family

Gazi tıp dergisi, 2019-01, Vol.30 (2), p.193-194

2019

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Association of a synonymous SCN1B variant affecting splicing efficiency with Benign Familial Infantile Epilepsy (BFIE)

European journal of paediatric neurology, 2017-09, Vol.21 (5), p.773-782

2017

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Paroxysmal posterior variant alien hand syndrome associated with parietal lobe infarction: case presentation

Cognitive neurodynamics, 2016-10, Vol.10 (5), p.453-455

2016

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Posterior reversible encephalopathy syndrome as an initial manifestation of systemic lupus erythematosus

Ideggyógyászati szemle, 2017-11, Vol.70 (11-12), p.425

2017

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Four novel and two recurrent NHLRC1 ( EPM2B ) and EPM2A gene mutations leading to Lafora disease in six Turkish families

Epilepsy research, 2012-02, Vol.98 (2), p.273-276

2012

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Atypical Features in a Large Turkish Family Affected with Friedreich Ataxia

Case reports in neurological medicine, 2016-01, Vol.2016 (2016), p.1-7

2016

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Serum Fetuin-A Levels in Patients with Bilateral Basal Ganglia Calcification

Neuroscience letters, 2018-02, Vol.666, p.148-152

2018

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Evaluation of Interictal Electroencephalography Findings in Patients with Focal Epilepsy: Does Secondary Bilateral Synchrony Play a Role on Seizure Frequency?

Archives of Epilepsy, 2020-01, Vol.26 (3), p.186-192

2020

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ERLIN1 mutations cause teenage-onset slowly progressive ALS in a large Turkish pedigree

European journal of human genetics : EJHG, 2018-05, Vol.26 (5), p.745-748

2018

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Seizure induced by extended-release bupropion used for smoking cessation at early term and therapeutic dose

Archives of Epilepsy, 2018-01, Vol.24 (3), p.127-129

Özözen Ayas, Zeynep

2018

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Dentatorubral pallidoluysian atrophy in a Turkish family

Turkish journal of pediatrics, 2009-11, Vol.51 (6), p.610-612

2009

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Successful treatment of Juvenile parkinsonism with bilateral subthalamic deep brain stimulation in a 14-year-old patient with parkin gene mutation

Parkinsonism & related disorders, 2016-03, Vol.24, p.137-138

2016

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The Evaluation of Botulinum Toxin Injection Effect for Poststroke Spasticity Treatment/Inme Sonrasi Spastisite Tedavisinde Botulinum Toksin Enjeksiyonu Etkinliginin Degerlendirilmesi

Türk nöroloji dergisi, 2017-03, Vol.23 (1), p.15

2017

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Coexistence of autosomal recessive spastic ataxia of Charlevoix Saguenay and spondyloepiphyseal dysplasia in a Turkish patient

Journal of the neurological sciences, 2015-10, Vol.357 (1), p.290-291

2015

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Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families

Neurology. Genetics, 2018-02, Vol.4 (1), p.e218-e218

2018

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Prevalence of carpal tunnel syndrome and its correlation with pain amongst female hairdressers

Quantitative phase imaging of erythrocyte in epilepsy patients

The effect of pelvic floor exercise program on incontinence and sexual dysfunction in multiple sclerosis patients

The Frequency of Fabry Disease among Young Cryptogenic Stroke Patients in the City of Sakarya

Clinical and molecular characterization and response to acitretin in three families with Sjögren‐Larsson syndrome

SCN1A GENE SEQUENCING IN 46 TURKISH EPILEPSY PATIENTS DISCLOSED 12 NOVEL MUTATIONS

Predictors of intensive care unit admission and mortality in patients with ischemic stroke: investigating the effects of a pulmonary rehabilitation program

Diaphragm pacing system implanted in a patient with ALS

The Evaluation of Botulinum Toxin Injection Effect for Poststroke Spasticity Treatment

The effect of cognitive performance on self-management behavior of multiple sclerosis patients

Autosomal Recessive Parkinson’s Disease with Early-Onset in a Turkish Family

Association of a synonymous SCN1B variant affecting splicing efficiency with Benign Familial Infantile Epilepsy (BFIE)

Paroxysmal posterior variant alien hand syndrome associated with parietal lobe infarction: case presentation

Posterior reversible encephalopathy syndrome as an initial manifestation of systemic lupus erythematosus

Four novel and two recurrent NHLRC1 ( EPM2B ) and EPM2A gene mutations leading to Lafora disease in six Turkish families

Atypical Features in a Large Turkish Family Affected with Friedreich Ataxia

Serum Fetuin-A Levels in Patients with Bilateral Basal Ganglia Calcification

Evaluation of Interictal Electroencephalography Findings in Patients with Focal Epilepsy: Does Secondary Bilateral Synchrony Play a Role on Seizure Frequency?

ERLIN1 mutations cause teenage-onset slowly progressive ALS in a large Turkish pedigree

Seizure induced by extended-release bupropion used for smoking cessation at early term and therapeutic dose

Dentatorubral pallidoluysian atrophy in a Turkish family

Successful treatment of Juvenile parkinsonism with bilateral subthalamic deep brain stimulation in a 14-year-old patient with parkin gene mutation

The Evaluation of Botulinum Toxin Injection Effect for Poststroke Spasticity Treatment/Inme Sonrasi Spastisite Tedavisinde Botulinum Toksin Enjeksiyonu Etkinliginin Degerlendirilmesi

Coexistence of autosomal recessive spastic ataxia of Charlevoix Saguenay and spondyloepiphyseal dysplasia in a Turkish patient

Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families

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