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Scientific Program

PDF (One Page) Turkish Program
18th April 2025, Friday
  Hall A   Hall B
08:15-08:30 Opening
Prof. Dr. Hacer Durmuş Tekçe
   
  RARE DISEASES AND NEUROGENETICS COURSE    
  BASIC GENETIC CONCEPTS FOR CLINICIANS
Chair: Prof. Dr. Oya Uyguner
   
08:30-09:00 Basic Genetic Concepts for Neurologists
Prof. Dr. Oya Uyguner
   
  DIAGNOSIS AND TREATMENT METHODS IN RARE DISEASES-1
Chair: Prof. Dr. Gülden Gökçay
   
09:00-09:20 Red Flags in Rare Diseases, Modifying Factors
Prof. Dr. Serdar Ceylaner
   
09:20-09:50 Approach to Rare Diseases: Three New Diseases, Three Stories
Prof. Dr. Ali Dursun
   
09:50-10:10 Expanded Screening Tests
Prof. Dr. Gülden Gökçay
   
10:10-10:30 Coffee Break
  BIOMARKERS AND PRECISION MEDICINE
Chair: Prof. Dr. Murat Terzi
   
10:30-10:50 Innovative Approaches in Neurogenetic Diseases: Metabolomics and Lipidomics
Prof. Dr. Asuman Gedikbaşı
   
10:50-11:10 Biomarkers in Neurodegeneration and Prion RT-QulC
Prof. Dr. Erdinç Dursun
   
11:10-11:30 The Future of Clinical Diagnosis: AI and Genomic Data for Precision Medicine
Prof. Dr. Murat Terzi
   
  DIAGNOSIS AND TREATMENT METHODS IN RARE DISEASES-2
Chair: Prof. Dr. Piraye Oflazer
   
11:30-11:40 Replacement Therapies in Hereditary Metabolic Diseases
Prof. Dr. Piraye Oflazer
   
11:40-12:00 ERT and Nucleoside Replacement Therapies in Hereditary Metabolic Diseases
Prof. Dr. Hacer Durmuş Tekçe
   
12:00-12:20 Gene Therapy in Hereditary Metabolic Diseases
Prof. Dr. Fatih Süheyl Ezgü
   
12:20-12:30 Questions and Discussions    
12:30-13:30 Lunch
13:30-14:00 CONFERENCE

Approach to Pediatric Neuromuscular Diseases

Prof. Dr. Haluk Topaloğlu
   
  SATELLITE SYMPOSIUM-1 / HUMANİS
From Diagnosis to Treatment of Cerebrotendinous Xanthomatosis

Chair: Prof. Dr. Gülden Gökçay
   
14:00-14:20 CTX from Pathophysiology to Treatment
Doç. Dr. Tanyel Zübarioğlu
   
14:20-14:40 CTX Clinical Spectrum
Prof. Dr. Haşmet Hanağası
   
15:00-17:30 WORKSHOP
NEUROGENETICS IN THE REGION


Neurogenetics in Pakistan
Flag of Pakistan Dr. Sara Khan

Neurogenetics in Kosovo
Flag of Kosovo Dr. Mehdi Šehu – Dr. Pranvera Bytyqi

Neurogenetics in Iraq
Flag of Iraq Dr. Saleh Salman Omairi

Neurogenetics in Azerbaijan
Flag of Azerbaijan Dr. Ilaha Elxan Hajiyeva

Neurogenetics in Hungary
Flag of Hungary Dr. Peter Balicza

Neurogenetics in North Macedonia
Flag of North Macedonia Dr. Shpresa Hasani

Neurogenetics in Bosnia and Herzegovina
Flag of Bosnia and Herzegovina Dr. Hamza Jatic

Neurogenetics in Montenegro
Flag of Montenegro Dr. Jovana Knezevic

15:00-17:30 Oral Presentations – 1
Chair: Dr. Birgül Baştan
19th April 2025, Saturday
  Hall A   Hall B
    08:00-09:00 Oral Presentations – 2
Chair: Dr. Ayşe Çağlar Sarılar
08:30-09:00 SEEING THE WHOLE PICTURE: AUTOIMMUNITY AND NEUROGENETICS
Chair: Prof. Dr. Filiz Koç

Overview of Neuroimmunogenetics
Prof. Dr. Serdar Ceylaner
  SATELLITE SYMPOSIUM-2 / CENTURION
GBS and Genetic Mimics

Chair: Prof. Dr. Filiz Koç
   
09:00-09:20 Guillian Barre Sendrom
Prof. Dr. Filiz Koç
   
09:20-09:40 Genetic Mimics of GBS
Doç.Dr.Ayşe Çağlar Sarılar
   
09:40-09:45 Questions and Discussions    
09:45-10:00 Coffee Break
  SATELLITE SYMPOSIUM-3 / DEM İLAÇ
CIDP and Genetic Mimics

Chair: Prof. Dr. Ersin Tan
   
10:00-10:20 Chronic Inflammatory Demyelinating PNP and Its Treatment
Prof. Dr. Ersin Tan
   
10:20-10:40 Genetic Mimics of CIDP
Prof. Dr. Can Ebru Kurt (Online)
   
10:40-11:00 MMN and Genetic Mimics
Prof. Dr. İhsan Şengün
   
11:00-11:10 Questions and Discussions    
  SATELLITE SYMPOSIUM-4 / ALEXION
Myasthenia Gravis and Genetic Mimics

Chair: Prof. Dr. Yeşim Parman
   
11:10-11:30 MG Pathophysiology and Complement Therapy
Prof. Dr. Yeşim Parman
   
11:30-11:50 Congenital Myasthenic Syndromes
Prof. Dr. Hacer Durmuş Tekçe
   
11:50-12:00 Questions and Discussion    
12:00-12:20 RNA CAR-T Therapy in Neurological Autoimmune Diseases
Metin Kurtoğlu
Chief Technology Officer, Cartesian Therapeutics
   
12:20-12:30 Questions and Discussion    
12:30-13:30 Lunch
  AUTOIMMUNE DISEASES OF THE CNS AND THEIR GENETIC BASIS
Chairs: Prof. Dr. Ahmet Gül, Prof. Dr. Aksel Siva
   
13:30-14:00 Genetic Basis of Behçet’s Disease
Prof. Dr. Ahmet Gül
   
14:00-14:20 Diagnosis and Treatment of Neuro-Behçet’s Disease
Prof. Dr. Aksel Siva
   
14:20-14:40 Genetic Basis of MS
Prof. Dr. Eda Tahir Turanlı
   
14:40-15:00 MS and Genetic Mimics
Prof. Dr. Serkan Demir
   
15:00-15:20 Coffee Break
  SEEING THE WHOLE PICTURE: NEURODEGENERATION – GENETIC AND METABOLIC FOUNDATIONS
Chairs: Prof. Dr. Ayşe Bora Tokçaer, Prof. Dr. Demet Özbabalık
   
15:20-15:40 Genetic Foundations of Parkinson’s Disease
Prof. Dr. Ayşe Bora Tokçaer
   
15:40-16:00 Genetic Foundations of Frontotemporal Dementia
Prof. Dr. Demet Özbabalık
   
16:00-16:20 Movement Disorders in Neurometabolic Diseases
Prof. Dr. Gencer Genç
   
16:20-16:40 Biotin-Thiamine Responsive Basal Ganglia Disease
Prof. Dr. Edibe Pembegül Yıldız
   
16:40-17:00 Neurodegenerative Diseases with Brain Iron Accumulation
Prof. Dr. Zuhal Yapıcı
   
17:00-17:20 Questions and Discussion    
20th April 2025, Sunday
  Hall A   Hall B
08:30-09:30 Oral Presentations – 3
Chairs: Dr. Sibel Uğur İşeri, Dr. Dilcan Kotan
     
  SEEING THE WHOLE PICTURE: GENETICS AND EPILEPSY
Chairs: Prof. Dr. Nerses Bebek, Prof. Dr. Sibel Uğur İşeri
   
09:30-09:50 Epileptic Encephalopathies
Prof. Dr. Nerses Bebek
   
09:50-10:10 Overview of the Genetic Origins of Epilepsy
Prof. Dr. Siber Uğur İşeri
   
10:10-10:30 Genetic Foundations of Sleep
Prof. Dr. Füsun Mayda Domaç
   
10:30-10:50 Real-World Data in SMA Treatments
Prof. Dr. Olcay Ünver
   
10:50-11:10 Coffee Break
  MEDICAL GENETICS ASSOCIATION SESSION
Chairs: Prof. Dr. Hacer Durmuş Tekçe, Prof. Dr. Taha Bahsi
   
11:10-11:30 The Importance of CNV (Copy Number Variations) in Neurogenetic Diseases
Doç. Dr. Ahmet Cevdet Ceylan
   
11:30-11:50 Neurometabolic and Neurogenetic Diseases Associated with Intracellular Trafficking Disorders
Dr. Öğr. Üyesi Ayça Dilruba Aslanger
   
11:50- 12:10 Genetic Factors Influencing Cerebrovascular Diseases
Dr. Öğr. Üyesi Erhan Parıltay
   
12:10-12:30 Questions and Discussion    
12:30-13:30 Lunch
  FROM PHENOTYPE TO GENOTYPE: TRINUCLEOTIDE REPEAT DISEASES
Chair: Prof. Dr. Dilcan Kotan
   
13:30:-13:50 Genetic Foundations of Repeat Expansion Diseases
Doç. Dr. Ebru Erzurumluoğlu
   
13:50-14:10 FRDA and Its Treatment
Prof. Dr. Banu Özen Barut
   
14:10-14:30 Huntington’s Disease and Repeat Expansion Ataxias
Doç. Dr. Nazlı Durmaz Çelik
   
14:30-14:50 Kennedy Disease
Doç. Dr. Arman Çakar
   
14:50-15:10 Myotonic Dystrophy
Prof. Dr. Dilcan Kotan
   
15:10-15:20 Rational Drug Use: Rational Use of Genetic Therapies
Doç. Dr. Birgül Baştan Tüzün
   
15:20-16:30 Oral Presentations – 4
Chairs: Prof.Dr. Dilcan Kotan, Prof.Dr. Sibel Uğur İşeri
   
16:30-17:00 Closing Ceremony
Prof. Dr. Hacer Durmuş Tekçe
   
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