Metrikler
Yayın
86
Açık Erişim
6
BM Sürdürülebilir Kalkınma Amaçları
Araştırma Alanları
Nöroloji
Akademik Ünvanlar / Görevler
2020 - Devam Ediyor
2020 - Devam EdiyorDr. Öğr. Üyesi
İstanbul Üniversitesi, İstanbul Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü
Akademi Dışı Deneyim
2023 - 2023
2023 - 2023Araştırma Görevlisi
UCL Queen Square Institute of Neurology, Araştırma Görevlisi
Makaleler
Tümü (59)
SCI-E, SSCI, AHCI (50)
SCI-E, SSCI, AHCI, ESCI (57)
ESCI (7)
Scopus (57)
TRDizin (12)
Diğer Yayınlar (1)
2025
20251. Biallelic variants in ARHGAP19 cause a progressive inherited motor-predominant neuropathy
Dominik N., Efthymiou S., Record C. J., Miao X., Lin R. Q., Parmar J. M., et al.
The Journal of clinical investigation
, cilt.135, sa.23, 2025 (SCI-Expanded, Scopus)
2025
20252. Eculizumab as a Rescue Therapy in Prolonged Myasthenic Crisis in the Intensive Care Unit: A Case Series
Durmus H., Çakar A., Gülşen Parman Y.
Neurocritical Care
, cilt.42, sa.3, ss.1099-1101, 2025 (SCI-Expanded)
2025
20253. Early Electrodiagnostic Study in Guillain-Barré Syndrome Requires a Second One for Accurate Electrodiagnosis.
Tasdemir V., Sirin N. G., Oge A. E., Cakar A., Culha A., Soysal A., et al.
Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society
, cilt.42, sa.5, ss.470-471, 2025 (SCI-Expanded)
2025
20254. Five-Year Results With Patisiran for Hereditary Transthyretin Amyloidosis With Polyneuropathy: A Randomized Clinical Trial With Open-Label Extension
Adams D., Wixner J., Polydefkis M., Berk J. L., Conceição I. M., Dispenzieri A., et al.
JAMA Neurology
, cilt.82, sa.3, ss.228-236, 2025 (SCI-Expanded)
2025
20255. Anti-Ri Associated Paraneoplastic Cervical Dystonia and Laryngospasm in a Patient with Nasopharyngeal Carcinoma.
Hanağasi H., Çakar A., Hanağasi F., Samanci B., Tüfekçioğlu Z., BİLGİÇ B., et al.
Noro psikiyatri arsivi
, cilt.62, sa.1, ss.94-96, 2025 (SCI-Expanded)
2025
20256. Genotype and phenotype spectrum of Charcot-Marie-Tooth disease due to mutations in SORD.
Cortese A., Dohrn M. F., Curro R., Negri S., Lassuthova P., Pisciotta C., et al.
Brain : a journal of neurology
, 2025 (SCI-Expanded)
2025
20257. Disease Progression in Charcot-Marie-Tooth Disease Type 4B (CMT4B) Associated With Mutations in Myotubularin-Related Proteins 2 and 13
Bertini A., Reilly M. M., Pisciotta C., Previtali S. C., Parman Y., Battaloglu E., et al.
European Journal of Neurology
, cilt.32, sa.2, 2025 (SCI-Expanded)
2025
20258. Delineating the genetic landscape of Charcot-Marie-tooth disease in Türkiye: Distinct distribution, rare phenotypes, and novel variants.
Cakar A., Candayan A., Bagırova G., UYGUNER Z. O., CEYLANER S., Durmus H., et al.
European journal of neurology
, cilt.32, sa.1, 2025 (SCI-Expanded)
2024
20249. Thymic gene expression analysis reveals a potential link between HIF-1A and Th17/Treg imbalance in thymoma associated myasthenia gravis
Altınönder İ., Kaya M., Yentür S. P., Çakar A., Durmuş H., Yegen G., et al.
Journal of Neuroinflammation
, cilt.21, sa.1, 2024 (SCI-Expanded)
2024
202410. In vitro modulation of T cells in myasthenia gravis by low-dose IL-2
Çebi M., Çakar A., Durmuş H., Akan O., Aysal F., Parman Y., et al.
European Journal of Immunology
, cilt.54, sa.11, 2024 (SCI-Expanded)
2024
202411. Eculizumab Versus Rituximab for Refractory Antiacetylcholine Receptor Antibody-Positive Generalized Myasthenia Gravis: A Single-Center Experience
DURMUŞ TEKÇE H., ÇAKAR A., Parman Y. G.
ACTA NEUROLOGICA SCANDINAVICA
, cilt.2024, 2024 (SCI-Expanded)
2024
202412. Clinical and neuroradiological spectrum of biallelic variants in NOTCH3
Iruzubieta P., Alves C. A. P. F., Al Shamsi A. M., ElGhazali G., Zaki M. S., Pinelli L., et al.
eBioMedicine
, cilt.107, 2024 (SCI-Expanded)
2024
202413. RTN2 deficiency results in an autosomal recessive distal motor neuropathy with lower limb spasticity
Maroofian R., Sarraf P., O'brien T. J., Kamel M., Cakar A., Elkhateeb N., et al.
Brain
, cilt.147, sa.7, ss.2334-2343, 2024 (SCI-Expanded)
2024
202414. Electrodiagnostic methods to verify Guillain-Barré syndrome subtypes in Istanbul: A prospective multicenter study
Tasdemir V., Sirin N. G., Cakar A., Culha A., Soysal A., Elmali A. D., et al.
JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM
, cilt.29, sa.1, ss.72-81, 2024 (SCI-Expanded)
2024
202415. Disease activity in chronic inflammatory demyelinating polyneuropathy: association between circulating B-cell subsets, cytokine levels, and clinical outcomes
Ozdag Acarli A. N., Tuzun E., Sanli E., Koral G., Akbayir E., Cakar A., et al.
CLINICAL AND EXPERIMENTAL IMMUNOLOGY
, cilt.215, sa.1, ss.65-78, 2024 (SCI-Expanded)
2024
202416. LETTER TO THE EDITOR Novel and nano-rare genetic causes of paediatric-onset motor neuronopathies
Cakar A., Maroofian R., Parman Y., Reilly M. M., Houlden H.
Brain Communications
, cilt.6, sa.1, 2024 (ESCI)
2024
202417. Autosomal recessive VWA1-related disorder: comprehensive analysis of phenotypic variability and genetic mutations
Nagy S., Pagnamenta A. T., Cali E., Braakman H. M., Wijntjes J., Kusters B., et al.
Brain Communications
, cilt.6, sa.6, 2024 (ESCI)
2023
202318. Genetic landscape of congenital insensitivity to pain and hereditary sensory and autonomic neuropathies.
Lischka A., Eggermann K., Record C. J., Dohrn M. F., Laššuthová P., Kraft F., et al.
Brain : a journal of neurology
, 2023 (SCI-Expanded)
2023
202319. Phenotypic features of RETREG1-related hereditary sensory autonomic neuropathy
Çakar A., Bagırova G., Durmuş H., Uyguner O., Parman Y.
Journal of the Peripheral Nervous System
, cilt.28, sa.3, ss.351-358, 2023 (SCI-Expanded)
2023
202320. Thymoma patients with or without myasthenia gravis have increased Th17 cells, IL-17 production and ICOS expression
Cebi M., Cakar A., Erdogdu E., Durmus-Tekce H., Yegen G., Ozkan B., et al.
JOURNAL OF NEUROIMMUNOLOGY
, 2023 (SCI-Expanded)
2023
202321. Pembrolizumab-induced peripheral nervous system damage: A combination of myositis/myasthenia overlap syndrome and motor axonal polyneuropathy Pembrolizumab által kiváltott perifériás idegrendszeri károsodás: A myositis / myasthenia overlap szindróma és a motoros axonalis polyneuropathia kombinációja
Arman Ç., Ibrahim K., Elif O. K., Hacer D., Yeşim P.
Ideggyogyaszati Szemle
, cilt.76, sa.11-12, ss.422-426, 2023 (SCI-Expanded)
2023
202322. A novel homozygous loss-of-function variant in SOD1 causing progressive spastic tetraplegia and axial hypotonia
Çakar A., Pekbilir E., CEYLANER S., Durmuş H., Battaloğlu E., Şahin U., et al.
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
, cilt.24, sa.5-6, ss.535-538, 2023 (SCI-Expanded)
2023
202323. Botulinum Toxin Treatment in Blepharospasm: Single-center Experience Blefarospazm Tedavisinde Botulinum Toksin: Tek-merkez Deneyimi
Çakar A., Samancı B., Hanağası H., Parman Y.
Turk Noroloji Dergisi
, cilt.29, sa.3, ss.204-208, 2023 (ESCI)
2022
202224. Disease activity in chronic inflammatory demyelinating polyneuropathy: A comparative study of clinical and skin biopsy markers
Acarli A. N. O., Unverengil G., Sirin N. G., Cakar A., Durmus H., Parman Y.
MUSCLE & NERVE
, cilt.66, sa.6, ss.736-743, 2022 (SCI-Expanded)
2022
202225. Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (canvas): an important cause of late-onset ataxia with unique clinical features
ÇAKAR A., Sahin E., Tezel S., Candayan A., Samanci B., BATTALOĞLU E., et al.
ACTA NEUROLOGICA BELGICA
, cilt.122, sa.4, ss.939-945, 2022 (SCI-Expanded)
2022
202226. AN EXPLORATORY STUDY OF COGNITIVE INVOLVEMENT IN HEREDITARY ATTRV
Durmus H., Cakar A., Demirci H., Parman Y.
JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM
, cilt.27, 2022 (SCI-Expanded)
2022
202227. NOVEL VARIANTS BROADEN THE MUTATIONAL SPECTRUM OF HEREDITARY SENSORY AND AUTONOMIC NEUROPATHY DISORDERS
Lischka A., Eggermann K., Cakar A., Record C., Elbracht M., Hornemann T., et al.
JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM
, cilt.27, 2022 (SCI-Expanded)
2022
202228. Genetic pain loss disorders
Lischka A., Lassuthova P., cakar A., Record C. J., Van Lent J., Baets J., et al.
NATURE REVIEWS DISEASE PRIMERS
, cilt.8, sa.1, 2022 (SCI-Expanded)
2022
202229. Phenotypical spectrum of SACS variants: Neuromuscular perspective of a complex neurodegenerative disorder
Cakar A., Inci M., Acarli A. N. O., Comu S., Candayan A., BATTALOĞLU E., et al.
ACTA NEUROLOGICA SCANDINAVICA
, cilt.145, ss.619-626, 2022 (SCI-Expanded)
2022
202230. Genetics of Pain: Novel variants identified by the European Network on Inherited Sensory Neuropathies and Insensitivity to Pain (ENISNIP)
Lischka A., Eggermann K., Cakar A., Bocek R., Bartesaghi L., Elbracht M., et al.
EUROPEAN JOURNAL OF HUMAN GENETICS
, cilt.30, sa.SUPPL 1, ss.128, 2022 (SCI-Expanded)
2022
202231. Lumbar Spinal Stenosis: A Rare Presentation of Hereditary Transthyretin Amyloidosis
Cakar A., Atmaca M. M., Kotan D., Durmus H., Deymeer F., Oflazer P., et al.
NOROPSIKIYATRI ARSIVI-ARCHIVES OF NEUROPSYCHIATRY
, cilt.59, sa.1, ss.77-79, 2022 (SCI-Expanded)
2022
202232. Comparison of Mitoxantrone versus Cyclophosphamide Treatment in Patients with Secondary Progressive Multiple Sclerosis
GÜNDÜZ T., ÖZCAN G., ÇAKAR A., AKÇAY H. İ., ÖZDAĞ ACARLI A. N., ERAKSOY M., et al.
Dicle Tıp Dergisi
, cilt.49, sa.1, ss.29-35, 2022 (Hakemli Dergi)
2021
202133. An Exploratory Study of Cognitive Involvement in Hereditary Transthyretin Amyloidosis
Durmus H., Cakar A., Demirci H., ALAYLIOĞLU M., GEZEN AK D., DURSUN E., et al.
ACTA NEUROLOGICA SCANDINAVICA
, cilt.144, sa.6, ss.640-646, 2021 (SCI-Expanded)
2021
202134. Genetic Survey of Autosomal Recessive Peripheral Neuropathy Cases Unravels High Genetic Heterogeneity in a Turkish Cohort
Candayan A., Çakar A., Yunisova G., Özdağ Acarlı A. N., Atkinson D., Topaloğlu P., et al.
NEUROLOGY-GENETICS
, cilt.7, sa.5, 2021 (SCI-Expanded)
2021
202135. Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (Canvas) is an important cause of late-onset ataxia
Cakar A., Sahin E., Tezel S., Candayan A., Samanci B., BATTALOĞLU E., et al.
JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM
, cilt.26, sa.3, ss.364, 2021 (SCI-Expanded)
2021
202136. Thymoma associated myasthenia gravis patients have increased Th17 Cells, IL-17 production and ICOS expression on CD4 T cells
Cebi M., ÇAKAR A., ERDOĞDU E., Tekce H. D., YEGEN G., ÖZKAN B., et al.
EUROPEAN JOURNAL OF IMMUNOLOGY
, cilt.51, ss.172, 2021 (SCI-Expanded)
2021
202137. The Complex Genetic Landscape of Hereditary Ataxias in Turkey and Implications in Clinical Practice
Vural A., Simsir G., Tekgul S., Kocoglu C., Akcimen F., Kartal E., et al.
MOVEMENT DISORDERS
, cilt.36, ss.1676-1688, 2021 (SCI-Expanded)
2021
202138. SOD1 Mutation: A Single Center Experience
ÇAKAR A., DURMUŞ TEKÇE H., PARMAN F. Y.
NEUROLOGY
, sa.15, 2021 (SCI-Expanded)
2021
202139. Late-onset TK2-Deficiency Patients from Turkey
DURMUŞ TEKÇE H., ÇAKAR A., PARMAN F. Y.
NEUROLOGY
, sa.15, 2021 (SCI-Expanded)
2021
202140. Clinical Features of the Patients with Neuromyelitis Optica Spectrum Disorder
Cakar A., Ulusoy C., Gunduz T., Kucukali C. I., Kurtuncu M.
NOROPSIKIYATRI ARSIVI-ARCHIVES OF NEUROPSYCHIATRY
, cilt.58, sa.1, ss.21-25, 2021 (SCI-Expanded)
2021
202141. Genotypic and phenotypic features of mutations in the HINT1 gene among Turkish patients with hereditary axonal neuropathy
Acarli A. O., Cakar A., Candayan A., Durmus H., Ceylaner S., Matur Z., et al.
JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM
, cilt.26, sa.1, ss.124-125, 2021 (SCI-Expanded)
2020
202042. Revisiting the complex architecture of ALS in Turkey: Expanding genotypes, shared phenotypes, molecular networks, and a public variant database
Tunca C., Seker T., Akcimen F., Coskun C., Bayraktar E., Palvadeau R., et al.
HUMAN MUTATION
, cilt.41, sa.8, 2020 (SCI-Expanded)
2020
202043. Aquaporin-4 Gene Polymorphisms in Neuromyelitis Optica and Recurrent Optic Neuritis
Çakar A., Ulusoy C. A., İplik E. S., Küçükali C. İ., Tüzün E., Kürtüncü M.
Turkish Journal of Neurology , cilt.26, sa.2, ss.127-130, 2020 (Hakemli Dergi)
2020
202044. Coronavirus Disease 2019 (COVID-19) From the Point of View of Neurologists: Observation of Neurological Findings and Symptoms During the Combat Against a Pandemic
Özdağ A. N., Samanci B., Ekizoğlu E., Çakar A., Şirin N. G., Gündüz T., et al.
NOROPSIKIYATRI ARSIVI-ARCHIVES OF NEUROPSYCHIATRY
, cilt.57, sa.2, ss.154-159, 2020 (SCI-Expanded)
2020
202045. The COVID-19 from Neurological Overview
Acar T., Demirel E. A., AFSAR N., AKÇALI A., Demir G. A., ALAGÖZ A. N., et al.
TURKISH JOURNAL OF NEUROLOGY
, cilt.26, sa.2, ss.58-108, 2020 (ESCI)
2020
202046. 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
Cebi M., DURMUŞ TEKÇE H., Aysal F., ÖZKAN B., Gul G. E., ÇAKAR A., et al.
Frontiers in Immunology
, cilt.11, 2020 (SCI-Expanded)
2020
202047. Aquaporin-4 Gene Polymorphisms in Neuromyelitis Optica and Recurrent Optic Neuritis
ÇAKAR A., ULUSOY C. A., BİRELLER E. S., KÜÇÜKALİ C. İ., TÜZÜN E., KÜRTÜNCÜ M.
TURKISH JOURNAL OF NEUROLOGY
, cilt.26, sa.2, ss.122-125, 2020 (ESCI)
2019
201948. A Val30Met sporadic familial amyloid polyneuropathy case with atypical presentation: upper limb onset of symptoms
Sahin E., Cakar A., Durmus-Tekce H., Parman Y.
ACTA NEUROLOGICA BELGICA
, cilt.119, sa.4, ss.627-628, 2019 (SCI-Expanded)
2019
201949. A novel homozygous FBXO38 variant causes an early-onset distal hereditary motor neuronopathy type IID.
Akcimen F., Vural A., Durmus H., Cakar A., Houlden H., Parman Y. G., et al.
Journal of human genetics
, cilt.64, sa.11, ss.1141-1144, 2019 (SCI-Expanded)
2019
201950. The first biallelic missense mutation in the FXN gene in a consanguineous Turkish family with Charcot-Marie-Tooth-like phenotype
Candayan A., Yunisova G., Cakar A., Durmus H., Basak A. N., Parman Y., et al.
NEUROGENETICS
, 2019 (SCI-Expanded)
2019
201951. Familial Amyloid Polyneuropathy
Cakar A., Durmus-Tekce H., Parman Y.
NOROPSIKIYATRI ARSIVI-ARCHIVES OF NEUROPSYCHIATRY
, cilt.56, sa.2, ss.150-156, 2019 (SCI-Expanded)
2018
201852. Paraplegia following lumbar puncture: a rare complication in spinal dural arteriovenous fistula
Cakar A., Akcay H. I., Gunduz T., Kurtuncu M.
ACTA NEUROLOGICA BELGICA
, cilt.118, sa.4, ss.543-545, 2018 (SCI-Expanded)
2018
201853. Orbital Myositis: An Underrecognized Clinical Syndrome with a Need of Management Guidelines
KIRAC L. B., Cakar A., TURKOGLU Y., AK H., COSKUN D., USTUN-OZEK S., et al.
CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES
, cilt.45, sa.1, ss.121-125, 2018 (SCI-Expanded)
2017
201754. Transthyretin-Related Familial Amyloid Polyneuropathy: In the Light of New Developments
Cakar A., Tekce H. D., Deymeer F., Serdaroglu P. O., Parman Y. G.
TURKISH JOURNAL OF NEUROLOGY
, cilt.23, sa.3, ss.105-111, 2017 (ESCI)
2016
201655. A HaNDL case with papilledema mimicking transient ischemic attack
Gungor I., Cakar A., Orhan E. K., Baykan B.
AGRI-THE JOURNAL OF THE TURKISH SOCIETY OF ALGOLOGY
, cilt.28, sa.4, ss.199-202, 2016 (ESCI)
2016
201656. Genotypic and phenotypic presentation of transthyretin-related familial amyloid polyneuropathy (TTR-FAP) in Turkey.
Durmus-Tekce H., MATUR Z., Atmaca M. M., Poda M., Cakar A., ULAS U. H., et al.
Neuromuscular disorders : NMD
, cilt.26, sa.7, ss.441-6, 2016 (SCI-Expanded)
2016
201657. Adult-onset phenylketonuria with rapidly progressive dementia and parkinsonism
Tufekcioglu Z., Cakar A., Bilgic B., Hanagasi H. A., Gurvit H., Emre M.
NEUROCASE
, cilt.22, sa.3, ss.273-275, 2016 (SCI-Expanded)
2016
201658. Genotypic and phenotypic presentation of TTR-FAP in Turkey
Durmus H., ÇAKAR A., Atmaca M. M., Matur Z., Altunoglu U., PODA M., et al.
EUROPEAN JOURNAL OF NEUROLOGY
, cilt.23, ss.341, 2016 (SCI-Expanded)
2016
201659. Temporary and Permanent Magnetic Resonance Imaging Findings in Status Epilepticus: Case Series
Atmaca M. M., Cakar A., Dede H. O., Bebek N., Gokyigit A., Gurses C.
JOURNAL OF NEUROLOGICAL SCIENCES-TURKISH
, cilt.33, sa.3, ss.507-514, 2016 (SCI-Expanded)
Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler
2024
20241. GENETIC LANDSCAPE OF CHARCOT-MARIE-TOOTH DISEASE IN TURKIYE: DISTINCT DISTRIBUTION, RARE PHENOTYPES, AND NOVEL VARIANTS
Çakar A., Candayan A., Bagirova G., Uyguner Z. O., Ceylaner S., Durmuş Tekçe H., et al.
Annual Meeting of the Peripheral-Nerve-Society (PNS), Montreal, Kanada, 22 - 25 Haziran 2024, cilt.29, ss.11, (Özet Bildiri)
2022
20222. Long-term follow-up of five families from Turkey with UBQLN2 variants
Durmus H., ÇAKAR A., Aysal F., Ertas M., Basak N., Parman Y.
21st Annual Meeting of the Northeast-Amyotrophic-Lateral-Sclerosis-Consortium (NEALS), Florida, Amerika Birleşik Devletleri, 1 - 03 Kasım 2022, (Özet Bildiri)
2016
20163. Paraplegia following lumbar puncture: a rare complication of spinal dural arteriovenous fistula
ÇAKAR A., AKÇAY H. İ., GÜNDÜZ T., KÜRTÜNCÜ M.
2nd Congress of European Academy of Neurology, Kopenhag, Danimarka, 28 - 31 Mayıs 2016, (Özet Bildiri)
2022
20224. TH-153. Clinical and electrophysiological characteristics of Guillain-Barré Syndrome before and during the pandemic: The multicenter Istanbul study
ŞİRİN İNAN N. G., TAŞDEMİR V., ÇAKAR A., ÇULHA OKTAR A., SOYSAL A., ELMALI YAZICI A. D., et al.
32nd International Congress of Clinical Neurophysiology (ICCN), Cenevre, İsviçre, 4 - 08 Eylül 2022, (Özet Bildiri)
2022
20225. An Exploratory Study of Cognitive Involvement in Hereditary Transthyretin Amyloidosis
Durmus H., ÇAKAR A., Demirci H., Parman F. Y.
Annual Meeting of the American-Academy-of-Neurology, Washington, Amerika Birleşik Devletleri, 2 - 07 Nisan 2022, (Özet Bildiri)
2021
20216. Pandemi Öncesi ve Pandemi Döneminde Guillain-Barré Sendromunun Klinik ve Elektrofizyolojik Özellikleri: Çok Merkezli İstanbul Çalışması
Taşdemir V., Şirin İnan N. G., Çakar A., Çulha A., Soysal A., Elmalı Yazıcı A. D., et al.
57. Ulusal Nöroloji Kongresi, Antalya, Türkiye, 27 Kasım - 01 Aralık 2021, (Yayınlanmadı)
2021
20217. YAYGIN HİPERPİGMENTASYON İLE BAŞVURAN BİR DERMATOMİYOZİT OLGUSU
GEZEGEN H., ALTINKAYNAK M., ÇAKAR A., DURMUŞ TEKÇE H., AKPINAR T. S., PARMAN F. Y.
57. Ulusal nöroloji kongresi, Antalya, Türkiye, 27 Kasım 2021, (Özet Bildiri)
2021
20218. Pandemi Öncesi ve Pandemi Döneminde Guillain-Barré Sendromunun Klinik ve Elektrofizyolojik Özellikleri: Çok Merkezli İstanbul Çalışması
TAŞDEMİR V., ŞİRİN N. G., ÇAKAR A., ÇULHA A., SOYSAL A., ELMALI A. D., et al.
57. Ulusal Nöroloji Kongresi, Antalya, Türkiye, 27 Kasım - 01 Aralık 2021, (Özet Bildiri)
2021
20219. Cognitive involvement in transthyretin-related familial amyloid polyneuropathy (TTR-FAP)
DURMUŞ TEKÇE H., ÇAKAR A., Demirci H., PARMAN F. Y.
Virtual Annual Meeting of the American-Academy-of-Neurology, ELECTR NETWORK, 17 - 22 Nisan 2021, (Özet Bildiri)
2021
202110. Expanding the phenotypical spectrum of SACS mutation: A Single Center Experience
ÇAKAR A., İNCİ M., ÖZDAĞ ACARLI A. N., DURMUŞ TEKÇE H., PARMAN F. Y.
Virtual Annual Meeting of the American-Academy-of-Neurology, ELECTR NETWORK, 17 - 22 Nisan 2021, (Özet Bildiri)
2021
202111. WRITER'S CRAMP: A SINGLE-CENTER EXPERIENCE
Cakar A., Tufekcioglu Z., Hanagasi H., Parman Y.
TOXINS Conference on Basic Science and Clinical Aspects of Botulinum and other Neurotoxins, ELECTR NETWORK, 16 - 17 Ocak 2021, cilt.190, (Özet Bildiri)
2020
202012. Cognitive involvement in ATTR amyloidosis (TTR-FAP)
DURMUŞ TEKÇE H., ÇAKAR A., Demirci H., Alaylioglu M., GEZEN AK D., DURSUN E., et al.
Virtual Conference of Peripheral-Nerve-Society, ELECTR NETWORK, 01 Ocak 2020, ss.527, (Özet Bildiri)
2020
202013. Clinical features of a homozygous missense mutation in the FXN gene resulting in a Charcot-Marie-Tooth-like phenotype
ÇAKAR A., Candayan A., Yunisova G., Battaloglu E., DURMUŞ TEKÇE H., PARMAN F. Y.
Virtual Conference of Peripheral-Nerve-Society, ELECTR NETWORK, 01 Ocak 2020, ss.490, (Özet Bildiri)
2020
202014. Circulating B Cell Subsets and Cytokine Gene Expression Levels in Peripheral Blood and Skin Biopsy in Chronic Inflammatory Demyelinating Polyneuropathy
Acarli A. N. O., Yilmaz V., Sirin N. G., ÇAKAR A., Soysal A., Aysal F., et al.
Annual Meeting of the American-Academy-of-Neurology, Toronto, Kanada, 25 Nisan - 01 Mayıs 2020, (Özet Bildiri)
2020
202015. Studying Clinical and Genetic Characteristics of Emery-Dreifuss Muscular Dystrophy
Yunisova G., Oflazer P., Deymeer F., ÇAKAR A., PARMAN F. Y., DURMUŞ TEKÇE H.
Annual Meeting of the American-Academy-of-Neurology, Toronto, Kanada, 25 Nisan - 01 Mayıs 2020, cilt.94, (Özet Bildiri)
2020
202016. Skin Biopsy as a Biomarker in Chronic Inflammatory Demyelinating Polyneuropathy
Parman Y., Acarli A. N. O., ÜNVERENGİL G., Sirin N. G., ÇAKAR A., DURMUŞ TEKÇE H.
Annual Meeting of the American-Academy-of-Neurology, Toronto, Kanada, 25 Nisan - 01 Mayıs 2020, (Özet Bildiri)
2020
202017. Clinical and genetic features of SPG11: A Single Center Experience
Cakar A., Gezegen H., Tunca C., Bayraktar E., Basak N., Durmus-Tekce H., et al.
Annual Meeting of the American-Academy-of-Neurology, Toronto, Kanada, 25 Nisan - 01 Mayıs 2020, cilt.94, (Özet Bildiri)
2019
201918. Autosomal Recessive Charcot-Marie-Tooth Disease in Turkey
Parman Y., Cakar A., Candayan A., Akcay H. I., Yunisova G., Ulukan Ç., et al.
71st Annual Meeting of the American-Academy-of-Neurology (AAN), Pennsylvania, Amerika Birleşik Devletleri, 4 - 10 Mayıs 2019, cilt.92, (Özet Bildiri)
2016
201619. Nöromiyelitis Optika Hastalarında Aquaporin-4 Gen Polimorfizmi
Cakar A., Ulusoy C., KÜÇÜKALİ C. İ., Tüzün E., Gündüz T., Kürtüncü M., et al.
52. Ulusal Nöroloji Kongresi, Antalya, Türkiye, 25 Kasım - 01 Aralık 2016, (Tam Metin Bildiri)
2016
201620. Comparison of Mitoxantrone versus Cyclophosphamide in Patients with Secondary Progressive Multiple Sclerosis
GÜNDÜZ T., ÖZCAN G., ÇAKAR A., AKÇAY H. İ., ÖZDAĞ ACARLI A. N., KÜRTÜNCÜ M., et al.
2nd Congress of European Academy of Neurology, Kopenhag, Danimarka, 28 - 31 Mayıs 2016, cilt.23, ss.601-879, (Özet Bildiri)
2016
201621. Clinical features of patients with relapsing inflammatory optic neuritis
Tuzun E., Cakar A., Akcay H. I., Kurtuncu M., Eraksoy M.
ACTRIMS Forum, Louisiana, Amerika Birleşik Devletleri, 18 - 20 Şubat 2016, cilt.22, ss.20-21, (Özet Bildiri)
2016
201622. Switching From Glatiramer Acetate: Comparison of Disease Modifying Treatments
Kurtuncu M., Akcay H. I., Cakar A., Gunduz T., Tuzun E., Eraksoy M.
ACTRIMS Forum, Louisiana, Amerika Birleşik Devletleri, 18 - 20 Şubat 2016, cilt.22, ss.18-19, (Özet Bildiri)
2015
201523. Genotypic and phenotypic presentation of Glu89Gln mutation in Turkey
DURMUŞ TEKÇE H., MATUR Z., ATMACA M. M., PODA M., ÇAKAR A., SERDAROĞLU OFLAZER P., et al.
First European Congress on Hereditary ATTR amyloidosis, Fransa, 2 - 03 Kasım 2015
2014
201424. Genotype-Phenotype Evaluation In 476 Turkish Dystrophinopathy Patients
Durmuş H., GEYİK F., ERGINEL-UENALTUNA N., PODA M., Çakar A., Altınkaya A., et al.
The 66th AAN Annual Meeting, Philadelphia, Amerika Birleşik Devletleri, 26 Nisan 2014 - 03 Mayıs 0215, ss.96, (Tam Metin Bildiri)
2013
201325. Karsinomatöz Menenjit Kliniği İle Başvuran Bir Glioblastom Olgusu
ÇAKAR A., KARAASLAN Z., BİRDAY E., ÇOBAN A., KÜRTÜNCÜ M.
49. Ulusal Nöroloji Kongresi, Türkiye, 15 Kasım 2013
2013
201326. Natalizumaba Bağlı Progresif Multifokal Lökoensefalopati Olgusu
ÇAKAR A., KARAASLAN Z., KARBAY M., BİRDAY E., ÇOBAN A., PEHLİVAN M., et al.
49. Ulusal Nöroloji Kongresi, Türkiye, 11 Kasım 2013
Kitaplar
2020
20201. Familial Amiloid Polinöropati - Dünya ve Türkiye Deneyimi Yeni Gelişmeler Işığında Transtiretin İlişkili Ailevi Amiloid Polinöropatisi
ÇAKAR A., DURMUŞ TEKÇE H., DEYMEER F., OFLAZER P., PARMAN F. Y.
Nadir Hastalıklar Pompe, Fabry ve TTR-FAP, Hilmi Uysal, Editör, Palme Yayınevi, Ankara, ss.177-190, 2020