Dr. Öğr. Üyesi Arman ÇAKAR

Yayın Ağı

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

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)

Late-onset TK2-Deficiency Patients from Turkey

DURMUŞ TEKÇE H., ÇAKAR A., PARMAN F. Y.

NEUROLOGY , sa.15, 2021 (SCI-Expanded)

SOD1 Mutation: A Single Center Experience

ÇAKAR A., DURMUŞ TEKÇE H., PARMAN F. Y.

NEUROLOGY , sa.15, 2021 (SCI-Expanded)

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)

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)

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)

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) Sürdürülebilir Kalkınma

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)

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)

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)

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)

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)

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)

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)

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)

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)

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) Sürdürülebilir Kalkınma

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)

Diğer Dergilerde Yayınlanan Makaleler

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)

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)

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)

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)

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) Sürdürülebilir Kalkınma

<i>Aquaporin</i>-<i>4</i> 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)

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)

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)

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

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

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

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

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

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

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

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

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

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

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

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

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

Kitap & Kitap Bölümleri

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

Metrikler

Yayın

Atıf (WoS)

158

H-İndeks (WoS)

Atıf (Scopus)

161

H-İndeks (Scopus)

Proje

Açık Erişim

BM Sürdürülebilir Kalkınma Amaçları

Yayınlar & Eserler