Publications & Works

Published journal articles indexed by SCI, SSCI, and AHCI

Articles Published in Other Journals

Nöropsikiyatri Arşivi , vol.40, no.1-2, pp.13-25, 2003 (Peer-Reviewed Journal)

Refereed Congress / Symposium Publications in Proceedings

Effects of TREM2 Homozygous Mutations (Nasu-Hakola Disease) on Natural Killer Cells

International Molecular Immunology & Immunogenetics Congress V, İzmir, Turkey, 20 - 22 October 2022, pp.42

Functional movement disorder in a cerebral palsy patient

2th International Congress on Psychopharmacology &8 th International Symposium on Child and Adolescent Psychopharmacology, Antalya, Turkey, 17 - 20 November 2021, pp.219

WRITER'S CRAMP: A SINGLE-CENTER EXPERIENCE

TOXINS Conference on Basic Science and Clinical Aspects of Botulinum and other Neurotoxins, ELECTR NETWORK, 16 - 17 January 2021, vol.190 identifier

Analysis of copy number variation in a Turkish dementia cohort

Alzheimer's Association International Conference (AAIC) , 27 - 31 July 2020, pp.44868

Cholesterol related gene polymorphisms in Alzheimer Disease

European Human Genetics Conference 2018, Milan, Italy, 16 - 19 June 2018, pp.1

Cholesterol related gene polymorphisms in Alzheimer Disease

51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, Italy, 16 - 19 June 2018, vol.27, pp.958 identifier

Assesment of candidate genes in patients with frontotemporal lobar degeneration spectrum: preliminary findings

51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, Italy, 16 - 19 June 2018, vol.27, pp.277-278 identifier

Türkiye Yaşlılarda Uygunsuz İlaç Kullanım Kriterleri - TIME Kriterleri

2. Uluslararası ve 12. Akademik Geriatri Kongresi, Antalya, Turkey, 24 - 28 April 2019, pp.1

TÜRK DEMANS HASTALARINDA FRONTO-TEMPORAL DEMANS İLE İLİŞKİLİ BAŞLICA GENLERDEKİ MUTASYON SIKLIĞI

Uluslararası Katılımlı 13. Ulusal Tıbbi Genetik Kongresi, Antalya, Turkey, 7 - 11 November 2018, pp.142

Cerebrotendinous Xanthomatosis: A Rare Lipid Storage Disease

International Congress of Parkinson's Disease and Movement Disorders, Hong Kong, Hong Kong, 5 - 09 October 2018, vol.33 identifier

Huntington's Disease in Turkey: A Bird's Eye Review of the Literature

International Congress of Parkinson's Disease and Movement Disorders, Hong Kong, Hong Kong, 5 - 09 October 2018, vol.33 identifier

Catatonia as clinical presentation of anti-n-methyl-d-aspartate (anti-NMDA) receptor encephalitis.

Alzheimer’s Association International Conference, Illinois, United States Of America, 22 - 26 July 2018, pp.1467-1468

Genetic Investigation in Parkinson Disease.

Erciyes Medical Genetics Days 2018, Kayseri, Turkey, 7 - 10 March 2018, vol.1, no.1, pp.52

Video-Oculography Assessment in Neurodegenerative Ataxias and Neimann Pick Type C

21st International Congress of Parkinson's Disease and Movement Disorders, Vancouver, Canada, 4 - 08 June 2017, vol.32 identifier

C19orf12 p.Thr11Met mutation is frequent among adult Turkish patients with MPAN

21st International Congress of Parkinson's Disease and Movement Disorders, Vancouver, Canada, 4 - 08 June 2017, vol.32 identifier

Diffusion discriminant for mild cognitive impairment in Parkinson’s disease

International Society of Magnetic Resonance in Medicine Annual Conference, Honolulu, Hı, United States Of America, 22 - 27 April 2017, pp.1

EFFECTS OF VARIOUS GRN VARIANTS ON MRNA AND SERUM PGRN LEVEL

3th International Conference on Alzheimer’s and Parkinson’s Diseases, Viyana, Austria, 29 March - 02 April 2017, pp.1674

GRN c.708 + 1_+4del TGAG deletion in a large family diagnosed with fronto-temporal dementia

10th International Conference on Frontotemporal Dementias, Münih, Germany, 31 August - 02 September 2016, vol.138, pp.323

GRN c.708+1_+4del TGAG deletion in a large family diagnosed with fronto-temporal dementia

10th International Conference on Frontotemporal Dementias, Munich, Germany, 31 August - 02 September 2016, vol.138, pp.323 identifier

Event-related Potentials as Potential Biomarkers for Cognitive Impairment in Parkinson’s Disease

22nd Annual Meeting of the Organization for Human Brain Mapping, Cenevre, Switzerland, 26 - 30 June 2016, pp.30

A novel homozygous DJ1 mutation causes Parkinsonism and ALS in a Turkish family

20th International Congress of Parkinson's Disease and Movement Disorders, Berlin, Germany, 19 - 23 June 2016, vol.31 identifier

Theta burst repetitive transcranial magnetic stimulation in a case with cortical-basal ganglionic degeneration

20th International Congress of Parkinson's Disease and Movement Disorders, Berlin, Germany, 19 - 23 June 2016, vol.31 identifier

Face and color recognition after subthalamic nucleus stimulation in Parkinson's disease

20th International Congress of Parkinson's Disease and Movement Disorders, Berlin, Germany, 19 - 23 June 2016, vol.31 identifier

A Case: Conversion Disorder with persistent movement disorder and ataxia

8th International Congress on Psychopharmacology & 4th International Symposium on Child and Adolescent Psychopharmacology, Antalya, Turkey, 20 - 24 April 2016, pp.15

Erken Başalayan Alzheimer Hastalığında PSEN1 ve APP Gen Mutasyonlarının Araştırılması

Uluslararası katkılı ‘Gevher Nesibe Günleri' 2016, Kayseri, Turkey, 11 - 13 February 2016, vol.38, no.1, pp.36

Clusterin polimorfizmleri ile geç başlangıçlı Alzheimer hastalığı arasındaki ilişki.

14. Ulusal Tıbbi Biyoloji ve Genetik Kongresi, Muğla, Turkey, 27 - 30 October 2015, vol.1, no.1, pp.1

PSEN1 mutation presenting as posterior cortical atrophy

22nd World Congress of Neurology (WCN), Santiago, Chile, 31 October - 05 November 2015, vol.357 identifier

Compromised Regulation of Serum Cytokine Levels and BDNF Due to Low Levels of Vitamin D in Patients with Early or Late Onset Alzheimer’s Disease or Parkinson’s Disease.

Alzheimer’s Association International Conference (AAIC 2015), 17-23 July, 2015 Washington, USA, Washington, United States Of America, 17 - 23 July 2015, pp.1-2

Association Between Clusterin Polymorphisms and Alzheimer’s Disease.

Alzheimer’s Association International Conference (AAIC 2015), 17-23 July, 2015 Washington, USA, Washington, United States Of America, 17 - 23 July 2015, pp.1

Secondary paroxysmal kinesigenic dyskinesia associated with CLCN2 gene mutation

19th International Congress of Parkinson's Disease and Movement Disorders, California, United States Of America, 14 - 18 June 2015, vol.30 identifier

Anti-NMDA receptor encephalitis with cancer of unknown primary origin

1st Congress of the European-Academy-of-Neurology, Berlin, Germany, 20 - 23 June 2015, vol.22, pp.526 Sustainable Development identifier

Adult onset phenylketonuria with rapidly progressive dementia and Parkinsonism

19th International Congress of Parkinson's Disease and Movement Disorders, California, United States Of America, 14 - 18 June 2015, vol.30 identifier

The distinct genetic pattern of ALS in Turkey

Joint Congress of European Neurology, İstanbul, Turkey, 31 May - 03 June 2014, vol.261 identifier

The distinct genetic pattern of ALS in Turkey

Joint Congress of European Neurology, İstanbul, Turkey, 31 May - 03 June 2014, vol.21, pp.63 identifier

Neuroacanthocytosis: A case report

18th International Congress of Parkinson's Disease and Movement Disorders, Stockholm, Sweden, 8 - 12 June 2014, vol.29 identifier

Testing of diagnostic criteria for mild cognitive impairment in patients with Parkinson's disease

18th International Congress of Parkinson's Disease and Movement Disorders, Stockholm, Sweden, 8 - 12 June 2014, vol.29 identifier

Serum complement factor H levels in late onset Alzheimer's disease

38th Congress of the Federation-of-European-Biochemical-Societies (FEBS), Saint Peter, Guernsey And Alderney, 6 - 11 July 2013, vol.280, pp.430 identifier

Investigation of SORL1 variants in a Turkish cohort of dementia patients

European Society of Human Genetics Congress, Paris, France, 8 - 11 June 2013, vol.21, pp.219

Evaluation of cognitive deficits in patients with parkin (PARK2) gene mutations using auditory event-related potentials

Turkish Society of Physiological Sciences and The Federation of European Physiological Societies (FEPS), Turkish-FEPS Physiology Congress, İstanbul, Turkey, 3 - 07 September 2011, vol.203, no.686, pp.137 Creative Commons License

Event-related potentials and oscillations during oddball task in parkinson patients with PARK2 gene mutations

7th Annual ECNS / ISNIP Conference, (ECNS) EEG & Clinical Neuroscience Society, (ISBET) lnternational Society for Brain Electromagnetic Topography, (lSNlP) lnternational Society for Neuroimaging in Psychiatry Joint Meeting., İstanbul, Turkey, 14 - 18 September 2010, vol.41, no.4, pp.46 Creative Commons License

Botulinum toxin injections for the facial region

20th Meeting of the European-Neurological-Society, Berlin, Germany, 19 - 23 June 2010, vol.257 identifier

Assessment of Cognitive Dysfunction in Parkinson Patients with Parkin Mutations by Neurophysiological Tests

Cognitive VII, International Cognitive Neuroscience Meeting, İstanbul, Turkey, 18 - 20 May 2010, vol.4, no.2, pp.41-43 Creative Commons License

9th National Congress of Neuroscience. , İstanbul, Turkey, 13 - 17 April 2010, vol.16, pp.212 Creative Commons License

Autosomal-recessive gene mutation frequencies in Turkish patients with Parkinson's disease

13th International Congress of Parkinsons Disease and Movement Disorders, Paris, France, 7 - 11 June 2009, vol.24 identifier

Ataxia with vitamin E deficiency in Turkey

12th International Congress of Parkinsons Disease and Movement Disorders, Illinois, United States Of America, 22 - 26 June 2008, vol.23 identifier

Clinical aspects of L-2-HGA disease in 13 Turkish children

17th Meeting of the European-Neurological-Society, Rhodes, Greece, 16 - 20 June 2007, vol.254, pp.97-98 identifier

Efficiency of botulinum toxin in treatment of writer's cramp: Long-term follow-up results

11th International Congress of Parkinsons Disease and Movement Disorders, İstanbul, Turkey, 3 - 07 June 2007, vol.22 identifier

Parkin immunolocalization in target fibers

11th International Congress on Neuromuscular Diseases, İstanbul, Turkey, 2 - 07 July 2006, vol.16 identifier

SNPs at the ligand binding site of the vitamin D receptor gene and Alzheimer’s disease.

10th International Conference on Alzheimer’s Disease and Related Disorders,, Spain, vol.2, no.3, pp.195-0

Auditory evoked N100 and P200 potantials in Alzeheimer’s disease

4th National Congress of Neuroscience, Mersin, Turkey, 29 March - 02 April 2005, vol.4, no.1, pp.8

Pain in Parkinson's disease

9th International Congress of Parkinsons Disease and Movement Disorders, Louisiana, United States Of America, 5 - 08 March 2005, vol.20 identifier

Presenilin-1 gene intronic polymorphism in late-onset Alzheimer's disease

9th International Conference on Alzheimers Disease and Related Disorders, Pennsylvania, United States Of America, 17 - 22 July 2004, vol.25 identifier

Auditory evoked N100 and P200 potantials in Alzeheimer’s disease

4th National Congress of Neuroscience, Mersin, Turkey, 29 March - 02 April 2004, vol.4, no.1, pp.8 Creative Commons License

Mitochondrial complex I activity in familial and sporadic Parkinson's disease

8th International Congress of Parkinsons Disease and Movement Disoders, Rome, Italy, 14 - 17 June 2004, vol.19 identifier

Mitochondrial complex II/III and complex IV activities in familial and sporadic Parkinson's disease

7th International Congress of Parkinsons Disease and Movement Disorders, MIAMI, FLORIDA, 10 - 14 November 2002, vol.17 identifier

Books & Book Chapters

. Dementia with Lewy bodies and Parkinson’s disease dementia

in: dementia, comprehensive princi.ples and practices, bradford Dickerson, Alireza Atri, Editor, Oxford University Press, London , Newyork, pp.231-259, 2014

Parkinson's Disease Dementia

in: Neuropsychiatric and Cognitive Changes in Parkinson's Disease and Related Movement Disorders, Aarsland D., Cummings J., Weintraub D., Chaudhur, R., Editor, Cambridge University Press, Cambridge (MA), USA , Newyork, pp.177-191, 2013

Tanıya genel yaklaşım, yardımcı tanı yöntemleri ve biyobelirteçler

in: Nöroloji Temel Kitabı, Emre M., Editor, Güneş Tıp Kitapevi Yayınları, Ankara, pp.951-955, 2012