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Thymic gene expression analysis reveals a potential link between HIF-1A and Th17/Treg imbalance in thymoma associated myasthenia gravis

Journal of neuroinflammation, 2024-05, Vol.21 (1), p.126-10, Article 126

2024

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CD4 + T Cells of Myasthenia Gravis Patients Are Characterized by Increased IL-21, IL-4, and IL-17A Productions and Higher Presence of PD-1 and ICOS

Frontiers in immunology, 2020-05, Vol.11, p.809-809

2020

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Disease activity in chronic inflammatory demyelinating polyneuropathy: A comparative study of clinical and skin biopsy markers

Muscle & nerve, 2022-12, Vol.66 (6), p.736-743

2022

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A novel homozygous FBXO38 variant causes an early-onset distal hereditary motor neuronopathy type IID

Journal of human genetics, 2019-11, Vol.64 (11), p.1141-1144

2019

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Genotypic and phenotypic presentation of transthyretin-related familial amyloid polyneuropathy (TTR-FAP) in Turkey

Neuromuscular disorders : NMD, 2016-07, Vol.26 (7), p.441-446

2016

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An Exploratory Study of Cognitive Involvement in Hereditary Transthyretin Amyloidosis

Acta neurologica Scandinavica, 2021-12, Vol.144 (6), p.640-646

2021

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Aquaporin-4 Gene Polymorphisms in Neuromyelitis Optica and Recurrent Optic Neuritis

Türk nöroloji dergisi, 2020-06, Vol.26 (2), p.122-125

2020

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Phenotypical spectrum of SACS variants: Neuromuscular perspective of a complex neurodegenerative disorder

Acta neurologica Scandinavica, 2022-05, Vol.145 (5), p.619-626

2022

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The first biallelic missense mutation in the FXN gene in a consanguineous Turkish family with Charcot-Marie-Tooth-like phenotype

Neurogenetics, 2020, Vol.21 (1), p.73-78

2020

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Coronavirus Disease 2019 (COVID-19) From the Point of View of Neurologists: Observation of Neurological Findings and Symptoms During the Combat Against a Pandemic

Noro-Psikiyatri Arsivi, 2020-06, Vol.57 (2), p.154-159

2020

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Revisiting the complex architecture of ALS in Turkey: Expanding genotypes, shared phenotypes, molecular networks, and a public variant database

Human mutation, 2020-08, Vol.41 (8), p.e7-e45

2020

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Transthyretin-Related Familial Amyloid Polyneuropathy: In the Light of New Developments

Türk nöroloji dergisi, 2017-09, Vol.23 (3), p.105-111

2017

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Genetic Survey of Autosomal Recessive Peripheral Neuropathy Cases Unravels High Genetic Heterogeneity in a Turkish Cohort

Neurology. Genetics, 2021-10, Vol.7 (5), p.e621-e621

2021

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Phenotypic features of RETREG1-related hereditary sensory autonomic neuropathy

Journal of the peripheral nervous system, 2023-09, Vol.28 (3), p.351-358

2023

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Botulinum Toxin Treatment in Blepharospasm: Single-center Experience

Türk nöroloji dergisi, 2023-09, Vol.29 (3), p.204-208

2023

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A novel homozygous loss-of-function variant in SOD1 causing progressive spastic tetraplegia and axial hypotonia

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2023-08, Vol.24 (5-6), p.535-538

2023

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Familial Amyloid Polyneuropathy

Noro-Psikiyatri Arsivi, 2019-06, Vol.56 (2), p.150-156

2019

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A Val30Met sporadic familial amyloid polyneuropathy case with atypical presentation: upper limb onset of symptoms

Acta neurologica Belgica, 2019-12, Vol.119 (4), p.627-628

2019

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Lumbar Spinal Stenosis: A Rare Presentation of Hereditary Transthyretin Amyloidosis

Noro-Psikiyatri Arsivi, 2022-03, Vol.59 (1), p.77-79

2022

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Clinical Features of the Patients with Neuromyelitis Optica Spectrum Disorder

Noro-Psikiyatri Arsivi, 2021-03, Vol.58 (1), p.21-25

2021

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Genetic pain loss disorders

Nature reviews. Disease primers, 2022-06, Vol.8 (1), p.41-41, Article 41

2022

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Paraplegia following lumbar puncture: a rare complication in spinal dural arteriovenous fistula

Acta neurologica Belgica, 2018-12, Vol.118 (4), p.543-545

2018

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Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (canvas): an important cause of late-onset ataxia with unique clinical features

Acta neurologica Belgica, 2022-08, Vol.122 (4), p.939-945

2022

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Nöromiyelitis Optika Spektrum Hastalığı Olan Hastaların Klinik Özellikleri

Noro-Psikiyatri Arsivi, 2021-03, Vol.58 (1), p.21-25

2021

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The COVID-19 from Neurological Overview

Türk nöroloji dergisi, 2020-06, Vol.26 (2), p.58-108

2020

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Thymic gene expression analysis reveals a potential link between HIF-1A and Th17/Treg imbalance in thymoma associated myasthenia gravis

CD4 + T Cells of Myasthenia Gravis Patients Are Characterized by Increased IL-21, IL-4, and IL-17A Productions and Higher Presence of PD-1 and ICOS

Disease activity in chronic inflammatory demyelinating polyneuropathy: A comparative study of clinical and skin biopsy markers

A novel homozygous FBXO38 variant causes an early-onset distal hereditary motor neuronopathy type IID

Genotypic and phenotypic presentation of transthyretin-related familial amyloid polyneuropathy (TTR-FAP) in Turkey

An Exploratory Study of Cognitive Involvement in Hereditary Transthyretin Amyloidosis

Aquaporin-4 Gene Polymorphisms in Neuromyelitis Optica and Recurrent Optic Neuritis

Phenotypical spectrum of SACS variants: Neuromuscular perspective of a complex neurodegenerative disorder

The first biallelic missense mutation in the FXN gene in a consanguineous Turkish family with Charcot-Marie-Tooth-like phenotype

Coronavirus Disease 2019 (COVID-19) From the Point of View of Neurologists: Observation of Neurological Findings and Symptoms During the Combat Against a Pandemic

Revisiting the complex architecture of ALS in Turkey: Expanding genotypes, shared phenotypes, molecular networks, and a public variant database

Transthyretin-Related Familial Amyloid Polyneuropathy: In the Light of New Developments

Genetic Survey of Autosomal Recessive Peripheral Neuropathy Cases Unravels High Genetic Heterogeneity in a Turkish Cohort

Phenotypic features of RETREG1-related hereditary sensory autonomic neuropathy

Botulinum Toxin Treatment in Blepharospasm: Single-center Experience

A novel homozygous loss-of-function variant in SOD1 causing progressive spastic tetraplegia and axial hypotonia

Familial Amyloid Polyneuropathy

A Val30Met sporadic familial amyloid polyneuropathy case with atypical presentation: upper limb onset of symptoms

Lumbar Spinal Stenosis: A Rare Presentation of Hereditary Transthyretin Amyloidosis

Clinical Features of the Patients with Neuromyelitis Optica Spectrum Disorder

Genetic pain loss disorders

Paraplegia following lumbar puncture: a rare complication in spinal dural arteriovenous fistula

Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (canvas): an important cause of late-onset ataxia with unique clinical features

Nöromiyelitis Optika Spektrum Hastalığı Olan Hastaların Klinik Özellikleri

The COVID-19 from Neurological Overview

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