Yayınlar & Eserler

Yayın Ağı
Makaleler 11
Tümü (11)
SCI-E, SSCI, AHCI (10)
SCI-E, SSCI, AHCI, ESCI (10)
Scopus (10)
TRDizin (3)

1. Congenital myasthenic syndromes in Türkiye: genetic and clinical spectrum revisited in a nationwide pediatric cohort

Üstün C., Polat İ., ÖZTÜRK G., ÜNVER O., TÜRKDOĞAN D., Kanmaz S., et al.
Neuromuscular Disorders , cilt.67, 2026 (SCI-Expanded, Scopus)

2. 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)

3. 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

4. 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)

5. 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 , cilt.48, 2025 (SCI-Expanded, Scopus)

6. 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)

7. 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

8. 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

9. 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)

10. 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

11. 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
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

35

Yayın (WoS)

29

Yayın (Scopus)

15

Atıf (WoS)

5

H-İndeks (WoS)

1

Atıf (Scopus)

25

H-İndeks (Scopus)

2

Proje

1

Açık Erişim

3
BM Sürdürülebilir Kalkınma Amaçları
SDG 3: AMAÇ 3: SAĞLIKLI BİREYLER
SDG 8: AMAÇ 8: İNSANA YAKIŞIR İŞ VE EKONOMİK BÜYÜME