Dr. Öğr. Üyesi ARMAN ÇAKAR

Yayın Ağı

Makaleler 66

1. REM-related obstructive sleep apnoea in neuromuscular diseases: A 10-year retrospective cohort study

Oguz M. S., Kiyan E., Pihtili A., Altan G., Cakar A., Durmus H.

Sleep and Breathing , cilt.30, sa.1, 2026 (SCI-Expanded, Scopus)

2. Charcot-Marie-Tooth–SORD: insights into pathology and pathophysiology from a human nerve biopsy series

Dohrn M. F., Pareyson D., Pisciotta C., Kölbel H., Roos A., Fabrizi G. M., et al.

Brain , cilt.149, sa.3, 2026 (SCI-Expanded, Scopus)

3. 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)

4. Sphingosine-1-Phosphate Phosphatase 1 Deficiency Leads to an Adult-Onset Hereditary Sensory Neuropathy with Mild Motor Involvement

ÇAKAR A., Bagirova G., GEDİKBAŞI A., KÜÇÜKGERGİN C., Giris M., DURMUŞ TEKÇE H., et al.

JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM , cilt.30, sa.3, ss.12-13, 2025 (SCI-Expanded, Scopus)

5. Biallelic Variants in ARHGAP19 Cause a Progressive Inherited Motor-Predominant Neuropathy-An Update

Dominik N., Efthymiou S., Record C., Miao X., Lin R., Parmar J., et al.

JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM , cilt.30, sa.3, ss.24-25, 2025 (SCI-Expanded, Scopus)

6. The Effect of Aerobic Exercise Training on Patients with Type III Spinal Muscular Atrophy

Mergen Kilic S., Mutluay F., Cakar A., Giris M., Durmus H., BİNGÜL İ., et al.

JOURNAL OF CLINICAL MEDICINE , cilt.14, sa.17, 2025 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

7. Unraveling the Genetic Landscape of Hereditary Sensory and Autonomic Neuropathy in Turkiye

ÇAKAR A., Bagirova G., DURMUŞ TEKÇE H., UYGUNER Z. O., PARMAN F. Y.

JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM , cilt.30, sa.3, ss.13, 2025 (SCI-Expanded, Scopus)

8. Genetic Heterogeneity of Distal Hereditary Motor Neuropathy in Turkiye: A Single Center Experience

ÇAKAR A., Candayan A., ERZURUMLUOĞLU GÖKALP E., DURMUŞ TEKÇE H., Houlden H., Battaloglu E., et al.

JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM , cilt.30, sa.3, ss.13, 2025 (SCI-Expanded, Scopus)

9. 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 , cilt.42, sa.5, ss.470-471, 2025 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma

10. 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, Scopus)

11. 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, Scopus)

12. Anti-Ri Associated Paraneoplastic Cervical Dystonia and Laryngospasm in a Patient with Nasopharyngeal Carcinoma.

Hanağasi H. A., 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, Scopus, TRDizin)

13. 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)

14. 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, Scopus)

15. 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, Scopus) Sürdürülebilir Kalkınma

16. 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, Scopus)

17. 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, Scopus) Sürdürülebilir Kalkınma

18. 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, Scopus)

19. 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, Scopus)

20. 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, Scopus)

21. 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, Scopus) Sürdürülebilir Kalkınma

22. 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, Scopus)

23. 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, Scopus) Sürdürülebilir Kalkınma

24. 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)

25. 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, Scopus)

26. 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, Scopus)

27. 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, Scopus)

28. 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, Scopus)

29. 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, Scopus, TRDizin)

30. 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, Scopus) Sürdürülebilir Kalkınma

31. 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, Scopus)

32. 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, Scopus)

33. 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)

34. 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, Scopus)

35. 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, Scopus)

36. 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, Scopus)

37. 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, Scopus)

38. 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 (TRDizin)

39. 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, Scopus, TRDizin)

40. 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, Scopus)

41. 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, Scopus)

42. 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, Scopus)

43. 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, Scopus)

44. 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, Scopus)

45. Late-onset TK2-Deficiency Patients from Turkey

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

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

46. SOD1 Mutation: A Single Center Experience

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

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

47. 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, Scopus)

48. 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, Scopus, TRDizin)

49. 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, Scopus)

50. 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)

51. 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, Scopus, TRDizin) Sürdürülebilir Kalkınma

52. 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, Scopus, TRDizin) Sürdürülebilir Kalkınma

53. 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, Scopus)

54. 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, Scopus, TRDizin)

55. 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, Scopus)

56. 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, Scopus)

57. 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, Scopus)

58. 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, Scopus, TRDizin)

59. 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, Scopus)

60. 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, Scopus)

61. 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, Scopus, TRDizin)

62. 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, Scopus, TRDizin)

63. 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, Scopus)

64. 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, Scopus)

65. 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, Scopus) Sürdürülebilir Kalkınma

66. 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, Scopus, TRDizin)

Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler 33

1. Botulinum Toksin Enjeksiyonu Polikliniğinde Hiperkinetik Hareket Bozukluğu: Klinik Özellikleri ve Tedavi Etkinliği Işığında Tek Merkez Deneyimi

Ateş D., Şahin E., Samancı B., Çakar A., Bilgiç B., Parman F. Y., et al.

61. Ulusal Nöroloji Kongresi, Antalya, Türkiye, 13 - 17 Aralık 2025, ss.741, (Özet Bildiri)

2. MME ilişkili Charcot-Marie-Tooth Hastalığı’nda Merkezi Sinir Sistemi Tutulumu Olgusu: Neden mi, Rastlantı mı?

Ateş D., Çakar A., Durmuş Tekçe H., Parman F. Y.

8. Nöromüsküler Hastalıklar Kongresi, Nevşehir, Türkiye, 2 - 05 Kasım 2025, ss.33, (Özet Bildiri)

3. **Characterization of clinical and genetic features of SIGMAR1-related disorder**

ÇAKAR A., Haridy N. A., TUNÇEL R., Soares Frezatti R. S., Tomaselli P. J., Villacorta A. S., et al.

58th Conference of the European-Society-of-Human-Genetics (ESHG), Milan, İtalya, 24 - 27 Mayıs 2025, cilt.33, ss.822, (Özet Bildiri)

4. Re-purposing Primidone as a RIPK1 inhibitor in OPTN-and TBK1-related ALS: a case series

DURMUŞ TEKÇE H., Gezen-AK D., DURSUN E., ÇAKAR A., KIYAN E., Parman Y. G.

30th Annual Congress of the World-Muscle-Society (WMS), Vienna, Avusturya, 7 - 11 Ekim 2025, cilt.53, (Özet Bildiri)

5. Eculizumab as a rescue therapy in myasthenic crisis in ICU: a case series

DURMUŞ TEKÇE H., ÇAKAR A., Parman Y. G.

30th Annual Congress of the World-Muscle-Society (WMS), Vienna, Avusturya, 7 - 11 Ekim 2025, cilt.53, (Özet Bildiri)

6. Clinical and Molecular Landscape of Amyotrophic Lateral Sclerosis Patients with OPTN Variants from Turkey and Possible Therapeutic Response to Inhibation of RIPK1

DURMUŞ TEKÇE H., ERZURUMLUOĞLU GÖKALP E., Gezenak D., Dursun E., Alaylioglu M., ÇAKAR A., et al.

Annual Meeting of the American-Academy-of-Neurology (AAN), California, Amerika Birleşik Devletleri, 5 - 09 Nisan 2025, cilt.104, (Özet Bildiri)

7. Riboflavin Responsive Slowly Progressive Early Onset Motor Neuron Disease Caused by a Novel Mutation in AIFM1

DURMUŞ TEKÇE H., ERZURUMLUOĞLU GÖKALP E., Ucar E. O., ÇAKAR A., Ceylaner S., Uyguner O., et al.

Annual Meeting of the American-Academy-of-Neurology (AAN), California, Amerika Birleşik Devletleri, 5 - 09 Nisan 2025, cilt.104, (Özet Bildiri)

8. 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)

9. 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)

10. 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)

11. 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)

12. 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)

13. 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)

14. 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)

15. 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)

16. 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)

17. 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)

18. 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)