Prof. CAN EBRU KURT

Publication Network

Published journal articles indexed by SCI, SSCI, and AHCI

The evaluation of small fibers in multiple sclerosis

Bekircan-Kurt C. E., Jahanroshan J., Tuncer A., ERGÜL ÜLGER Z., Gunes G., ERDEM ÖZDAMAR S., et al.

Multiple Sclerosis and Related Disorders, vol.72, 2023 (SCI-Expanded)

Nusinersen for adults with spinal muscular atrophy

ARSLAN D., İNAN B., KILINÇ M., Bekircan-Kurt C. E., ERDEM ÖZDAMAR S., Tan E.

Neurological Sciences, 2023 (SCI-Expanded)

Two distinct skeletal muscle microRNA signatures revealing the complex mechanism of sporadic ALS

AKSU MENGEŞ E., Balci-Hayta B., Bekircan-Kurt C. E., Aydinoglu A. T., ERDEM ÖZDAMAR S., Tan E.

ACTA NEUROLOGICA BELGICA, vol.122, no.6, pp.1499-1509, 2022 (SCI-Expanded)

Comprehensive evaluation of velopharyngeal function in myasthenia gravis patients

BAŞTUĞ DUMBAK A., KULAK KAYIKCI M. E., ŞAHİN M. İ., KUŞCU O., Bekircan-Kurt C. E., ERDEM ÖZDAMAR S.

ACTA NEUROLOGICA BELGICA, vol.122, no.5, pp.1229-1236, 2022 (SCI-Expanded)

The functional and structural evaluation of small fibers in asymptomatic carriers of TTR p.Val50Met (Val30Met) mutation

Bekircan-Kurt C. E., YILMAZ E., ARSLAN D., Yildiz F. G., DİKMETAŞ Ö., ERGÜL ÜLGER Z., et al.

NEUROMUSCULAR DISORDERS, vol.32, no.1, pp.50-56, 2022 (SCI-Expanded) Sustainable Development

Eculizumab in refractory generalized myasthenia gravis previously treated with rituximab: subgroup analysis of REGAIN and its extension study

Siddiqi Z. A., Nowak R. J., Mozaffar T., O'Brien F., Yountz M., Patti F., et al.

Muscle and Nerve, vol.64, no.6, pp.662-669, 2021 (SCI-Expanded)

Biologia Futura: the importance of 3D organoids-a new approach for research on neurological and rare diseases

AKBABA T. H., Bekircan-Kurt C. E., Balci-Peynircioglu B., Balci-Hayta B.

BIOLOGIA FUTURA, vol.72, no.3, pp.281-290, 2021 (SCI-Expanded)

The evaluation of small fibers in asymptomatic carriers of Val30Met mutation: Results of three years follow-up

Bekircan-Kurt C. E., YILMAZ E., Aslan D., Yildiz F. G., DİKMETAŞ Ö., ERGÜL ÜLGER Z., et al.

JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, vol.26, no.3, pp.379, 2021 (SCI-Expanded)

One Disease with two Faces: Semidominant Inheritance of a Novel HTRA1 Mutation in a Consanguineous Family

Bekircan-Kurt C. E., ÇETİNKAYA A., GÖÇMEN R., KOŞUKCU C., Soylemezoglu F., ARSAVA E. M., et al.

JOURNAL OF STROKE & CEREBROVASCULAR DISEASES, vol.30, no.9, 2021 (SCI-Expanded)

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

KARANFİL E., SALCI Y., FİL BALKAN A., Bekircan-Kurt C. E., ERDEM ÖZDAMAR S., ARMUTLU K.

OTJR-OCCUPATION PARTICIPATION AND HEALTH, vol.41, no.2, pp.101-107, 2021 (SSCI)

Consistent improvement with eculizumab across muscle groups in myasthenia gravis

Mantegazza R., O'Brien F. L., Yountz M., Howard J. F., Gabriel Mazia C., Wilken M., et al.

Annals of Clinical and Translational Neurology, vol.7, no.8, pp.1327-1339, 2020 (SCI-Expanded)

Trigeminal sensory-motor neuropathy in a patient with mixed connective tissue disease and review of the literature

Bekircan-Kurt C. E., TEMUÇİN Ç. M., APRAŞ BİLGEN Ş. Ş., ERDEM ÖZDAMAR S.

NEUROLOGICAL SCIENCES AND NEUROPHYSIOLOGY, vol.37, no.3, pp.148-151, 2020 (SCI-Expanded)

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

Bulduk B. K., Kilic H. B., Bekircan-Kurt C. E., Haliloglu G., ERDEM ÖZDAMAR S., Topaloglu H., et al.

GENETIC TESTING AND MOLECULAR BIOMARKERS, vol.24, no.3, pp.165-170, 2020 (SCI-Expanded)

Giant cell myositis associated with myasthenia gravis and thymoma

İNAN B., KURT C. E., Yildiz F. G., ERDEM ÖZDAMAR S., TEMUÇİN Ç. M., Tan E.

NEUROLOGICAL SCIENCES AND NEUROPHYSIOLOGY, vol.36, no.4, pp.236-237, 2019 (SCI-Expanded)

Laboratory diagnosis of metachromatic leukodystrophy requires more than arylsulfatase A assay

Pekgul F., Bekircan-Kurt C. E., Konuskan B., Erdem-Ozdamar S., Tan E., Akarsu N., et al.

FEBS OPEN BIO, vol.9, pp.199, 2019 (SCI-Expanded)

Two sisters with anti-MuSK-positive myasthenia gravis

KURT E., Bekircan-Kurt C. E., KONUŞKAN B., ERKENT ERCAN İ., Tan E., Anlar B.

CLINICAL NEUROLOGY AND NEUROSURGERY, vol.182, pp.17-18, 2019 (SCI-Expanded)

Long-term safety and efficacy of eculizumab in generalized myasthenia gravis

Muppidi S., Utsugisawa K., Benatar M., Murai H., Barohn R. J., Illa I., et al.

Muscle and Nerve, vol.60, no.1, pp.14-24, 2019 (SCI-Expanded)

Establishment of primary myoblast cell cultures from cryopreserved skeletal muscle biopsies to serve as a tool in related research & development studies

Balci-Hayta B., Bekircan-Kurt C. E., AKSU MENGEŞ E., DAYANGAÇ ERDEN D., Tan E., ERDEM ÖZDAMAR S.

JOURNAL OF THE NEUROLOGICAL SCIENCES, vol.393, pp.100-104, 2018 (SCI-Expanded)

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

Gunes H. N., Bekircan-Kurt C. E., Tan E., ERDEM ÖZDAMAR S.

ACTA NEUROLOGICA BELGICA, vol.118, no.3, pp.405-410, 2018 (SCI-Expanded) Sustainable Development

Ocular surface alterations and in vivo confocal microscopic characteristics of corneas in patients with myasthenia gravis

ERKAN TURAN K., KOCABEYOĞLU S., Bekircan-Kurt C. E., BEZCİ F., ERDEM ÖZDAMAR S., Irkec M.

EUROPEAN JOURNAL OF OPHTHALMOLOGY, vol.28, no.5, pp.541-546, 2018 (SCI-Expanded)

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

Tunca C., Akcimen F., Coskun C., Gundogdu-Eken A., Kocoglu C., ÇEVİK B., et al.

EUROPEAN JOURNAL OF HUMAN GENETICS, vol.26, no.5, pp.745-748, 2018 (SCI-Expanded)

Safety and efficacy of eculizumab in anti-acetylcholine receptor antibody-positive refractory generalised myasthenia gravis (REGAIN): a phase 3, randomised, double-blind, placebo-controlled, multicentre study

Howard J. F., Utsugisawa K., Benatar M., Murai H., Barohn R. J., Illa I., et al.

The Lancet Neurology, vol.16, no.12, pp.976-986, 2017 (SCI-Expanded) Sustainable Development

Myophosphorylase (PYGM) mutations determined by next generation sequencing in a cohort from Turkey with McArdle disease

Inal-Gultekin G., Toptas-Hekimoglu B., Gormez Z., Gelisin O., Durmus H., Erguner B., et al.

NEUROMUSCULAR DISORDERS, vol.27, no.11, pp.997-1008, 2017 (SCI-Expanded)

CELLULAR INFILTRATES IN SKIN AND SURAL NERVE OF PATIENTS WITH POLYNEUROPATHIES

Ueceyler N., Braunsdorf S., Kunze E., Riediger N., Scheytt S., Divisova S., et al.

MUSCLE & NERVE, vol.55, no.6, pp.884-893, 2017 (SCI-Expanded)

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

Bekircan-Kurt C. E., Gunes H. N., Yildiz F. G., SAKA TOPÇUOĞLU E., Tan E., ERDEM ÖZDAMAR S.

ACTA NEUROLOGICA BELGICA, vol.117, no.1, pp.269-275, 2017 (SCI-Expanded)

Single-pulse Transcranial Magnetic Stimulation in Amyotrophic Lateral Sclerosis: Experience of a single institution

Yildiz F. G., Bekircan-Kurt C. E., VARLI K.

JOURNAL OF NEUROLOGICAL SCIENCES-TURKISH, vol.34, no.1, pp.70-75, 2017 (SCI-Expanded)

The evaluation of small fibres in asymptomatic patients with Val30Met mutation

Bekircan-Kurt C. E., Yildiz F. G., Gunes H. N., Erdem-Ozdamar S., Tan E.

EUROPEAN JOURNAL OF NEUROLOGY, vol.23, pp.231, 2016 (SCI-Expanded)

Autoimmune storm

Aslan S., Bekircan-Kurt C. E., Kurne A. T., Erdem-Ozdamar S.

EUROPEAN JOURNAL OF NEUROLOGY, vol.23, pp.437, 2016 (SCI-Expanded)

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

BORA-TATAR G., YESBEK-KAYMAZ A., BEKIRCAN-KURT C. E., ERDEM-OZDAMAR S., Erdem-Yurter H.

EUROPEAN JOURNAL OF MEDICAL GENETICS, vol.58, no.12, pp.654-658, 2015 (SCI-Expanded)

Three Turkish families with different transthyretin mutations

Bekirean-Kurt C. E., GUNES N., Yilmaz A., ERDEM-OZDAMAR S., TAN E.

NEUROMUSCULAR DISORDERS, vol.25, no.9, pp.686-692, 2015 (SCI-Expanded)

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

Bekircan-Kurt C. E., TAN E., OZDAMAR S. E.

NOROPSIKIYATRI ARSIVI-ARCHIVES OF NEUROPSYCHIATRY, vol.52, no.3, pp.279-282, 2015 (SCI-Expanded)

Voltage gated calcium channel antibody-related neurological diseases.

Bekircan-Kurt C. E., Derle Ç., KURNE A., ANLAR B.

World journal of clinical cases, vol.3, pp.293-300, 2015 (SCI-Expanded)

CUTANEOUS ACTIVATION OF RAGE IN NONSYSTEMIC VASCULITIC AND DIABETIC NEUROPATHY

Bekircan-Kurt C. E., Ueceyler N., SOMMER C.

MUSCLE & NERVE, vol.50, no.3, pp.377-383, 2014 (SCI-Expanded) Sustainable Development

The Course of Myasthenia Gravis with Systemic Lupus Erythematosus

Bekircan-Kurt C. E., Kurne A. T., Erdem-Ozdamar S., Kalyoncu U., Karabudak R., Tan E.

EUROPEAN NEUROLOGY, vol.72, pp.326-329, 2014 (SCI-Expanded)

'Jaw clenching' in anti-Ri - Antibody-associated paraneoplastic syndrome

Bekircan-Kurt C. E., TEMUÇİN Ç. M., ELİBOL B., SAKA E.

PARKINSONISM & RELATED DISORDERS, vol.19, no.1, pp.132-133, 2013 (SCI-Expanded)

Myasthenia Gravis; Single Entity, Variable Clinical Features: Ten Years of Clinical Experience in a Tertiary Care Center Ten Years Clinical Experience of a Tertiary Care Center

BEKIRCAN-KURT C. E., KURNE A., ERDEM ÖZDAMAR S., KARABUDAK R., KANSU T., TAN E.

JOURNAL OF NEUROLOGICAL SCIENCES-TURKISH, vol.30, no.1, pp.135-143, 2013 (SCI-Expanded)

Articles Published in Other Journals

Identifying a Cut-off Point for Timed Up and Go Test in Neuromuscular Diseases

Demirci C. S., SÜTÇÜ G., AYVAT F., ONURSAL KILINÇ Ö., DOĞAN M., AYVAT E., et al.

TURKISH JOURNAL OF NEUROLOGY, vol.28, no.1, pp.6-9, 2022 (ESCI)

A Rare Cause of Dystonia: Spinal Meningioma

Sarayli A. A. K., Bekircan-Kurt C. E., GÖÇMEN R., ÖGE H. K., Tan E.

TURKISH JOURNAL OF NEUROLOGY, vol.27, no.2, pp.215-216, 2021 (ESCI)

Organelle Positioning in Neurons and Skeletal Muscle Cells

AKSU MENGEŞ E., KURAL MANGIT E., Bekircan-Kurt C. E., BORA G.

GAZI MEDICAL JOURNAL, vol.32, pp.341-347, 2021 (ESCI)

Psychosocial Adjustment and Adherence to Medication in Patients with Myasthenia Gravis

AŞİRET G. D., KAPUCU S., KAYMAZ T. T., Bekircan-Kurt C. E.

GAZI MEDICAL JOURNAL, vol.32, no.3, pp.371-376, 2021 (ESCI)

Dysferlinopathy: A Case Report and Literature Update

Kutlu O., KURT C. E., Unsal I., Aribas Z., Renkliyildiz B., Eruzun H., et al.

ISTANBUL MEDICAL JOURNAL, vol.17, no.4, pp.136-140, 2016 (ESCI)

Refereed Congress / Symposium Publications in Proceedings

MME MUTASYONUNA BAĞLI DEMİYELİNİZAN NÖROPATİ

Demirel Özbek E., ERGÜL ÜLGER Z., TAN M. E., ERDEM ÖZDAMAR S., KURT C. E.

58. Ulusal Nöroloji Kongresi, Antalya, Turkey, 19 - 24 November 2022

The evaluation of small fibers in asymptomatic carriers of Val30Met mutation: Results of three years follow-up

KURT C. E., YILMAZ E., aslan d., YILDIZ SARIKAYA F. G., DİKMETAŞ Ö., ERGÜL ÜLGER Z., et al.

2021 PNS Annual Meeting, United States Of America, 12 - 26 June 2021, vol.26, pp.379-179

Multimodal Assessment of Intensive Care Unit- Acquired Weakness in Severe Stroke Patients

İNAN B., KURT C. E., ERGÜL ÜLGER Z., yılmaz m.

2021 American Academy of Neurology, 2 - 10 April 2021

The effect and challenges of nusinersen treatment in adult spinal muscular atrophy patients - preliminary results

Inan B., Bekircan-Kurt C. E., Kilinc M., Erdem-Ozdamar S., Tan E.

6th Congress of the European-Academy-of-Neurology (EAN), ELECTR NETWORK, 23 - 26 May 2020, vol.27, pp.625