Prof. Dr. CAN EBRU KURT

Yayın Ağı

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

Transitioning From Nusinersen to Risdiplam for Spinal Muscular Atrophy in Clinical Practice: A Single-Center Experience

KURT C. E., Subramanian S., Chagat S., Mackenzie S. J., Iammarino M., Reash N., et al.

MUSCLE & NERVE , sa.3, ss.414-421, 2025 (SCI-Expanded)

Clinical and laboratory remission with rituximab in anti-MuSK-positive myasthenia gravis

İNAN B., ORHAN İ. G., KURT C. E., ERDEM ÖZDAMAR S., Tan E.

IRISH JOURNAL OF MEDICAL SCIENCE , cilt.193, ss.2989-2994, 2024 (SCI-Expanded)

A novel pathogenic <i>PTRH2</i> variant indicates seizure association with protein-truncating variants in Infantile-Onset Multisystem Neurologic, Endocrine and Pancreatic Disease (IMNEPD)

AKÇİN Ö. Ç., KURTÇU O., DERİCİOĞLU N., ERDEM ÖZDAMAR S., KURT C. E., ALTINER Ş., et al.

EUROPEAN JOURNAL OF HUMAN GENETICS , ss.1494, 2024 (SCI-Expanded)

Effect of Follicular T Helper and T Helper 17 Cells-Related Molecules on Disease Severity in Patients with Myasthenia Gravis

ARSLAN D., ERGÜL ÜLGER Z., Goksen S., ESENDAĞLI G., ERDEM ÖZDAMAR S., Tan E., et al.

EUROPEAN NEUROLOGY , cilt.87, sa.5-6, ss.223-229, 2024 (SCI-Expanded)

A novel pathogenic PTRH2 variant indicates seizure association with protein-truncating variants in Infantile-Onset Multisystem Neurologic, Endocrine and Pancreatic Disease (IMNEPD)

AKÇİN Ö. Ç., KURTÇU O., DERİCİOĞLU N., ERDEM ÖZDAMAR S., KURT C. E., ALTINER Ş., et al.

EUROPEAN JOURNAL OF HUMAN GENETICS , ss.1494, 2024 (SCI-Expanded)

Differentiating recurrent Guillain-Barre syndrome and acute-onset chronic inflammatory polyneuropathy: literature review

İNAN B., KURT C. E., Demirci M., ERDEM ÖZDAMAR S., Tan E.

ACTA NEUROLOGICA BELGICA , cilt.124, ss.1467-1475, 2024 (SCI-Expanded) Sürdürülebilir Kalkınma

VARIABLE PHENOTYPE IN FEMALES WITH HETEROZYGOUS GJB1 MUTATION

KURT C. E., ERGÜL ÜLGER Z., TEMUÇİN Ç. M., Kumtepe E. T., BALCI B., Tan E., et al.

JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM , 2024 (SCI-Expanded)

Recurrent simultaneous central nervous system demyelination with possible peripheral demyelination / nodopathy in a seronegative patient

İNAN B., KURT C. E., YILDIZ SARIKAYA F. G., GÖÇMEN R., TEMUÇİN Ç. M., Tuncer A., et al.

IDEGGYOGYASZATI SZEMLE-CLINICAL NEUROSCIENCE , cilt.77, sa.9-10, ss.357-360, 2024 (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 , cilt.44, sa.7, ss.2393-2400, 2023 (SCI-Expanded)

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 , cilt.72, 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 , cilt.122, sa.6, ss.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 , cilt.122, sa.5, ss.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 , cilt.32, sa.1, ss.50-56, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma

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 , cilt.64, sa.6, ss.662-669, 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 , cilt.26, sa.3, ss.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 , cilt.30, sa.9, 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 , cilt.72, sa.3, ss.281-290, 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 , cilt.41, sa.2, ss.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 , cilt.7, sa.8, ss.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 , cilt.37, sa.3, ss.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 , cilt.24, sa.3, ss.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 , cilt.36, sa.4, ss.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 , cilt.9, ss.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 , cilt.182, ss.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 , cilt.60, sa.1, ss.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 , cilt.393, ss.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 , cilt.118, sa.3, ss.405-410, 2018 (SCI-Expanded) Sürdürülebilir Kalkınma

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 , cilt.28, sa.5, ss.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 , cilt.26, sa.5, ss.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 , cilt.16, sa.12, ss.976-986, 2017 (SCI-Expanded) Sürdürülebilir Kalkınma

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 , cilt.27, sa.11, ss.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 , cilt.55, sa.6, ss.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 , cilt.117, sa.1, ss.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 , cilt.34, sa.1, ss.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 , cilt.23, ss.231, 2016 (SCI-Expanded)

Autoimmune storm

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

EUROPEAN JOURNAL OF NEUROLOGY , cilt.23, ss.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 , cilt.58, sa.12, ss.654-658, 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 , cilt.52, sa.3, ss.279-282, 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 , cilt.25, sa.9, ss.686-692, 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 , cilt.3, ss.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 , cilt.50, sa.3, ss.377-383, 2014 (SCI-Expanded) Sürdürülebilir Kalkınma

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 , cilt.72, ss.326-329, 2014 (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 , cilt.30, sa.1, ss.135-143, 2013 (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 , cilt.19, sa.1, ss.132-133, 2013 (SCI-Expanded)

Diğer Dergilerde Yayınlanan Makaleler

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 , cilt.28, sa.1, ss.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 , cilt.27, sa.2, ss.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 , cilt.32, ss.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 , cilt.32, sa.3, ss.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 , cilt.17, sa.4, ss.136-140, 2016 (ESCI)

Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler

NUSİNERSEN TEDAVİSİ ALAN ERİŞKİN SPİNAL MUSKÜLER ATROFİ HASTALARINDA İNFLAMASYON VE GLİAL HÜCRE İLİŞKİLİ BİYOBELİRTEÇLERİN TESPİTİ

ARSLAN D., ERGÜL ÜLGER Z., gökşen s., ESENDAĞLI G., ERDEM ÖZDAMAR S., TAN M. E., et al.

59. Ulusal Nöroloji Kongresi, Antalya, Türkiye, 13 Aralık 2023

MİYASTENİK KRİZ İLE BAŞVURAN HASTALARDA YARDIMCI FOLİKÜLER T HÜCRE (TFH) VE YARDIMCI T HÜCRE 17 (TH17) İLİŞKİLİ SİTOKİNLERİN TEDAVİ ÖNCESİ VE SONRASI DEĞİŞKENLİĞİ

ARSLAN D., ERGÜL ÜLGER Z., gökşen s., ESENDAĞLI G., ERDEM ÖZDAMAR S., TAN M. E., et al.

59. Ulusal Nöroloji Kongresi, Antalya, Türkiye, 13 Aralık 2023

Evaluation of the Role of Glial Factors in the Pathogenesis of Spinal Muscular Atrophy

ARSLAN D., ERGÜL ÜLGER Z., gökşen s., İNAN B., ESENDAĞLI G., ERDEM ÖZDAMAR S., et al.

2023 Neuromuscular Study Group Meeting, Orlando, Amerika Birleşik Devletleri, 22 Eylül 2023

Serum Cytokines Levels in Patients with Myasthenia Gravis and Their Changes After Treatment

ARSLAN D., ERGÜL ÜLGER Z., gökşen s., ESENDAĞLI G., ERDEM ÖZDAMAR S., TAN M. E., et al.

75th Annual Meeting of the American-Academy-of-Neurology (AAN), Boston, Amerika Birleşik Devletleri, 22 Nisan 2023

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, Türkiye, 19 - 24 Kasım 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, Amerika Birleşik Devletleri, 12 - 26 Haziran 2021, cilt.26, ss.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 Nisan 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 Mayıs 2020, cilt.27, ss.625