Çakar A - Search Results

1

Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (canvas): an important cause of late-onset ataxia with unique clinical features.

Çakar A, Şahin E, Tezel S, Candayan A, Samancı B, Battaloğlu E, Başak AN, Bilgiç B, Hanağası H, Durmuş H, Parman Y. Çakar A, et al. Acta Neurol Belg. 2022 Aug;122(4):939-945. doi: 10.1007/s13760-021-01721-2. Epub 2021 Jun 8. Acta Neurol Belg. 2022. PMID: 34101140

2

Adult-onset phenylketonuria with rapidly progressive dementia and parkinsonism.

Tufekcioglu Z, Cakar A, Bilgic B, Hanagasi H, Gurvit H, Emre M. Tufekcioglu Z, et al. Among authors: cakar a. Neurocase. 2016 Jun;22(3):273-5. doi: 10.1080/13554794.2016.1142567. Epub 2016 Mar 10. Neurocase. 2016. PMID: 26962957

3

Genotypic and phenotypic presentation of transthyretin-related familial amyloid polyneuropathy (TTR-FAP) in Turkey.

Durmuş-Tekçe H, Matur Z, Mert Atmaca M, Poda M, Çakar A, Hıdır Ulaş Ü, Oflazer-Serdaroğlu P, Deymeer F, Parman YG. Durmuş-Tekçe H, et al. Among authors: cakar a. Neuromuscul Disord. 2016 Jul;26(7):441-6. doi: 10.1016/j.nmd.2016.04.013. Epub 2016 May 5. Neuromuscul Disord. 2016. PMID: 27238058

4

Paraplegia following lumbar puncture: a rare complication in spinal dural arteriovenous fistula.

Çakar A, Akçay Hİ, Gündüz T, Kürtüncü M. Çakar A, et al. Acta Neurol Belg. 2018 Dec;118(4):543-545. doi: 10.1007/s13760-018-0951-7. Epub 2018 May 28. Acta Neurol Belg. 2018. PMID: 29808310 No abstract available.

5

A Val30Met sporadic familial amyloid polyneuropathy case with atypical presentation: upper limb onset of symptoms.

Şahin E, Çakar A, Durmuş-Tekçe H, Parman Y. Şahin E, et al. Among authors: cakar a. Acta Neurol Belg. 2019 Dec;119(4):627-628. doi: 10.1007/s13760-018-0959-z. Epub 2018 Jun 5. Acta Neurol Belg. 2019. PMID: 29873031 No abstract available.

6

Familial Amyloid Polyneuropathy.

Çakar A, Durmuş-Tekçe H, Parman Y. Çakar A, et al. Noro Psikiyatr Ars. 2019 May 6;56(2):150-156. doi: 10.29399/npa.23502. eCollection 2019 Jun. Noro Psikiyatr Ars. 2019. PMID: 31223250 Free PMC article. Review.

7

A novel homozygous FBXO38 variant causes an early-onset distal hereditary motor neuronopathy type IID.

Akçimen F, Vural A, Durmuş H, Çakar A, Houlden H, Parman YG, Nazlı Başak A. Akçimen F, et al. Among authors: cakar a. J Hum Genet. 2019 Nov;64(11):1141-1144. doi: 10.1038/s10038-019-0652-y. Epub 2019 Aug 17. J Hum Genet. 2019. PMID: 31420593

8

The first biallelic missense mutation in the FXN gene in a consanguineous Turkish family with Charcot-Marie-Tooth-like phenotype.

Candayan A, Yunisova G, Çakar A, Durmuş H, Başak AN, Parman Y, Battaloğlu E. Candayan A, et al. Among authors: cakar a. Neurogenetics. 2020 Jan;21(1):73-78. doi: 10.1007/s10048-019-00594-1. Epub 2019 Oct 31. Neurogenetics. 2020. PMID: 31673878

9

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.

Çebi M, Durmus H, Aysal F, Özkan B, Gül GE, Çakar A, Hocaoglu M, Mercan M, Yentür SP, Tütüncü M, Yayla V, Akan O, Dogan Ö, Parman Y, Saruhan-Direskeneli G. Çebi M, et al. Among authors: cakar a. Front Immunol. 2020 May 19;11:809. doi: 10.3389/fimmu.2020.00809. eCollection 2020. Front Immunol. 2020. PMID: 32508812 Free PMC article.

10

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 Acarli AN, Samanci B, Ekizoğlu E, Çakar A, Şirin NG, Gündüz T, Parman Y, Baykan B. Özdağ Acarli AN, et al. Among authors: cakar a. Noro Psikiyatr Ars. 2020 May 1;57(2):154-159. doi: 10.29399/npa.26148. eCollection 2020 Jun. Noro Psikiyatr Ars. 2020. PMID: 32550783 Free PMC article. Review.

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