Yayınlar & Eserler

Yayın Ağı
Makaleler 10
Tümü (10)
SCI-E, SSCI, AHCI (9)
SCI-E, SSCI, AHCI, ESCI (9)
Scopus (9)
TRDizin (3)

1. Phenotypic continuum in IGHMBP2-related disorders: a portfolio of cases from typical to Guillain-Barré syndrome-like presentation

Bektaş H., Şener N., Bilgin N., ÜREL DEMİR G., Öncel İ., ÖZTOPRAK Ü., et al.
Neuromuscular Disorders , cilt.59, 2026 (SCI-Expanded, Scopus) identifier identifier

2. Assessment of cardiac involvement in childhood neurofibromatosis type 1 diagnoses, identification of Rasopathic Cases

tekdemir i. e., Kayılıoğlu H., Doğan V., Aksoy A., Öztoprak Ü., aksoy e., et al.
Health sciences quarterly (Online) , cilt.6, sa.1, ss.139-146, 2026 (TRDizin) Creative Commons License identifier

3. Long-Term Clinical Characterization of ENTPD1-Related Spastic Paraplegia: A Novel Variant and Comprehensive Literature Review

ERKAN KOLAÇ D. D., Lafci O., ÖZTOPRAK Ü., Haliloglu G., GÜLERAY LAFCI N.
INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE , cilt.85, sa.5, 2025 (SCI-Expanded, Scopus) identifier identifier

4. Neurogenic arthrogryposis, hypotonia, dysmorphic features plus malformation of cortical development further expands the ARL6IP1 loss-of-function phenotype

Haliloglu G., Donkervoort S., ÖZTOPRAK Ü., Osei-Owusu I. A., Pais L., Devrez F. D., et al.
NEUROMUSCULAR DISORDERS , 2025 (SCI-Expanded, Scopus) identifier identifier

5. Frequency and Characteristics of Sleep Apnea Syndrome in Pediatric Patients with Duchenne Muscular Dystrophy

Yavuz B. C., Yildiz S. O., Buyuksahin H. N., ÖZEL E., EMİRALİOĞLU ORDUKAYA N., AYKAN H. H., et al.
EUROPEAN RESPIRATORY JOURNAL , 2024 (SCI-Expanded, Scopus) identifier

6. Re-examining the characteristics of pediatric multiple sclerosis in the era of antibody-associated demyelinating syndromes

Yilmaz U., GÜCÜYENER K., Yavuz M., Oncel İ. H., CANPOLAT M., Saltik S., et al.
EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , ss.8-18, 2022 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

7. Expanding the genotype-phenotype spectrum of autosomal recessive Charcot-Marie-Tooth disease: A novel PLEKHG5 gene mutation

Yayici Koken O., Oztoprak Ü., Topcu V., Cavdarli B., Temuçin Ç. M., Aydıngöz Ü., et al.
NEUROLOGY ASIA , cilt.26, sa.3, ss.607-612, 2021 (SCI-Expanded, Scopus) Creative Commons License identifier identifier

8. Acute necrotizing encephalopathy of childhood: a single-center experience

Aksoy E., Oztoprak Ü., Celik H., Ozdemir F. M. A., Ozkan M., Kayalioglu H., et al.
TURKISH JOURNAL OF MEDICAL SCIENCES , cilt.51, sa.2, ss.706-715, 2021 (SCI-Expanded, Scopus, TRDizin) identifier identifier identifier identifier

9. Clinical presentation of anti-N-methyl-D-aspartate receptor and anti-voltage-gated potassium channel complex antibodies in children: A series of 24 cases

Konuskan B., Yildirim M., Topaloglu H., Erol I., Oztoprak Ü., Tan H., et al.
EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY , cilt.22, sa.1, ss.135-142, 2018 (SCI-Expanded, Scopus) Sürdürülebilir Kalkınma identifier identifier identifier

10. The seizure semiology consistent with frontal lobe symptomatogenic zone in children

Oztoprak Ü., Yalnızoğlu D., Oguz K. K., Ergün E., Soylemezoglu F., Bilginer B., et al.
TURKISH JOURNAL OF PEDIATRICS , cilt.58, sa.6, ss.583-591, 2016 (SCI-Expanded, Scopus, TRDizin) Creative Commons License identifier identifier
Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler 1

1. Clinical course and treatment outcome in children with Rasmussen Encephalitis

ÖZTOPRAK Ü., TEZER FİLİK F. İ., GÜNBEY C., BİLGİNER B., GÖÇMEN R., KARLI OĞUZ H. K., et al.
15th European Paediatric Neurology Society Congress, prague, Çek Cumhuriyeti, 20 - 24 Haziran 2023, (Özet Bildiri)
Metrikler

Yayın

33

Yayın (WoS)

27

Yayın (Scopus)

13

Atıf (WoS)

5

H-İndeks (WoS)

1

Atıf (Scopus)

16

H-İndeks (Scopus)

1

Proje

1

Açık Erişim

3
BM Sürdürülebilir Kalkınma Amaçları