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Transcript levels of plastin 3 and neuritin 1 modifier genes in spinal muscular atrophy siblings

Pediatrics international, 2017-01, Vol.59 (1), p.53-56

2017

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Identifying A Cut-Off Point for Timed Up and Go Test in Neuromuscular Diseases

Türk nöroloji dergisi, 2022-03, Vol.28 (1), p.6-9

2022

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Remission with fingolimod in a case of demyelinating polyneuropathy

Muscle & nerve, 2014-10, Vol.50 (4), p.615-617

2014

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Fulminant Central Plus Peripheral Nervous System Demyelination without Antibodies to Neurofascin

Canadian journal of neurological sciences, 2016-01, Vol.43 (1), p.149-156

2016

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The Neurophysiologic Frequency of Hereditary Neuropathy with Liability to Pressure Palsy in Entrapment Neuropathies

Türk nöroloji dergisi, 2016-12, Vol.22 (4), p.177-180

2016

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Overexpression of amyloid beta precursor protein enhances expression and secretion of ST6Gal1 in C2C12 myogenic cell line

Cell biology international, 2011-01, Vol.35 (1), p.9-13

2011

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Proinflammatory effect of AbetaPP induced ST6GAL1 secretion from C2C12 myogenic cell line / [C2C12 miyojenik hücre hattında AbetaPP tarafından indüklenen ST6GAL1 salgılanmasının proinflamatuar etkisi]

Turkish Journal of Biochemistry, 2015-01, Vol.40 (1), p.31-36

2015

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Toscana virus associated with Guillain–Barré syndrome: a case–control study

Acta neurologica Belgica, 2021-06, Vol.121 (3), p.661-668

2021

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The histopathological evaluation of small fiber neuropathy in patients with vitamin B12 deficiency

Acta neurologica Belgica, 2018-09, Vol.118 (3), p.405-410

2018

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Comprehensive evaluation of velopharyngeal function in myasthenia gravis patients

Acta neurologica Belgica, 2022-10, Vol.122 (5), p.1229-1236

2022

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Expert opinion on the diagnostic odyssey and management of late-onset Pompe disease: a neurologist's perspective

Frontiers in neurology, 2023-05, Vol.14, p.1095134-1095134

2023

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Autologous Stem Cell Transplantation in a Patient with Refractory anti-MuSK-Positive Myasthenia Gravis and Familial Mediterranean Fever

Neurological sciences and neurophysiology, 2022-04, Vol.39 (2), p.115-118

2022

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A Novel Amplification-Refractory Mutation System-PCR Strategy to Screen MT-TL1 Pathogenic Variants in Patient Repositories

Genetic testing and molecular biomarkers, 2020-03, Vol.24 (3), p.165-170

2020

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Reliability and Validity of Turkish Myasthenia Gravis-Activities of Daily Living Scale

OTJR (Thorofare, N.J.), 2021-04, Vol.41 (2), p.101-107

2021

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Three Turkish families with different transthyretin mutations

Neuromuscular disorders : NMD, 2015-09, Vol.25 (9), p.686-692

2015

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Spinal muscular atrophy type III: Molecular genetic characterization of Turkish patients

European journal of medical genetics, 2015-12, Vol.58 (12), p.654-658

2015

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New mutations and genotype–phenotype correlation in late-onset Pompe patients

Acta neurologica Belgica, 2017-03, Vol.117 (1), p.269-275

2017

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Recent therapeutic developments in spinal muscular atrophy

Turkish journal of medical sciences, 2018-04, Vol.48 (2), p.203-211

2018

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Giant cell myositis associated with myasthenia gravis and thymoma

Neurological sciences and neurophysiology, 2019-12, Vol.36 (4), p.236-237

2019

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S39 Familial amyloid polyneuropathy (FAP): All aspects of the disease from diagnosis to treatment: Disease description: What is FAP?

Clinical neurophysiology, 2017-09, Vol.128 (9), p.e192-e192

Özdamar, Sevim Erdem

2017

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The Activation of RAGE and NF-KB in Nerve Biopsies of Patients with Axonal and Vasculitic Neuropathy

Noro-Psikiyatri Arsivi, 2015-09, Vol.52 (3), p.279-282

2015

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Brachial Diparesis due to Motor Neuronopathy as One of the Predominant Presenting Signs of Occult Small Cell Lung Carcinoma

Internal Medicine, 2016/06/15, Vol.55(12), pp.1641-1643

2016

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The effects of spinal stabilization exercises in patients with myasthenia gravis: a randomized crossover study

Disability and rehabilitation, 2022-12, Vol.44 (26), p.8442-8449

2022

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Dysferlinopathy: A Case Report and Literature Update

Istanbul medical journal, 2016-12, p.136-140

2016

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Diabetic muscular infarct: an unusual cause of extremity pain and dysfunction

Rheumatology international, 2012-02, Vol.32 (2), p.525-528

2012

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Transcript levels of plastin 3 and neuritin 1 modifier genes in spinal muscular atrophy siblings

Identifying A Cut-Off Point for Timed Up and Go Test in Neuromuscular Diseases

Remission with fingolimod in a case of demyelinating polyneuropathy

Fulminant Central Plus Peripheral Nervous System Demyelination without Antibodies to Neurofascin

The Neurophysiologic Frequency of Hereditary Neuropathy with Liability to Pressure Palsy in Entrapment Neuropathies

Overexpression of amyloid beta precursor protein enhances expression and secretion of ST6Gal1 in C2C12 myogenic cell line

Proinflammatory effect of AbetaPP induced ST6GAL1 secretion from C2C12 myogenic cell line / [C2C12 miyojenik hücre hattında AbetaPP tarafından indüklenen ST6GAL1 salgılanmasının proinflamatuar etkisi]

Toscana virus associated with Guillain–Barré syndrome: a case–control study

The histopathological evaluation of small fiber neuropathy in patients with vitamin B12 deficiency

Comprehensive evaluation of velopharyngeal function in myasthenia gravis patients

Expert opinion on the diagnostic odyssey and management of late-onset Pompe disease: a neurologist's perspective

Autologous Stem Cell Transplantation in a Patient with Refractory anti-MuSK-Positive Myasthenia Gravis and Familial Mediterranean Fever

A Novel Amplification-Refractory Mutation System-PCR Strategy to Screen MT-TL1 Pathogenic Variants in Patient Repositories

Reliability and Validity of Turkish Myasthenia Gravis-Activities of Daily Living Scale

Three Turkish families with different transthyretin mutations

Spinal muscular atrophy type III: Molecular genetic characterization of Turkish patients

New mutations and genotype–phenotype correlation in late-onset Pompe patients

Recent therapeutic developments in spinal muscular atrophy

Giant cell myositis associated with myasthenia gravis and thymoma

S39 Familial amyloid polyneuropathy (FAP): All aspects of the disease from diagnosis to treatment: Disease description: What is FAP?

The Activation of RAGE and NF-KB in Nerve Biopsies of Patients with Axonal and Vasculitic Neuropathy

Brachial Diparesis due to Motor Neuronopathy as One of the Predominant Presenting Signs of Occult Small Cell Lung Carcinoma

The effects of spinal stabilization exercises in patients with myasthenia gravis: a randomized crossover study

Dysferlinopathy: A Case Report and Literature Update

Diabetic muscular infarct: an unusual cause of extremity pain and dysfunction

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