Doç. Dr. Pakize KARAOĞLU

1. Ultrasonographic assessment of subarachnoid space width in healthy infants aged 0–3 months: normative data and associations with anthropometric parameters

Çolak E., KARAOĞLU P., Karaman H. H., ÜNALP A., ORBATU D.

Child's Nervous System , cilt.42, sa.1, 2026 (SCI-Expanded, Scopus)

2. The efficacy and tolerability of lacosamide adjunctive therapy in children with drug-refractory epilepsy: A nationwide Turkish cohort study

Kart P. O., SERDAROĞLU E., Yildiz N., Kılıç R. K., Sari M., Sahin S., et al.

Epilepsy and Behavior , cilt.179, 2026 (SCI-Expanded, Scopus)

3. Electroencephalogram abnormalities in children presenting with language development delay

Yavuz M., Gülağız F., ÜNALP A., KARAOĞLU P., YILMAZ Ü.

Brain and Development , cilt.48, sa.1, 2026 (SCI-Expanded, Scopus)

4. The Clinical and Molecular Spectrum of Patients With X-Linked Intellectual Disability and Novel Variations in Different Genes

GÜRSOY S., Yılmaz Uzman C., Erdoğan K. M., KARAOĞLU P., Sözen Türk T., YILMAZ Ü., et al.

Pediatric Neurology , cilt.165, ss.43-51, 2025 (SCI-Expanded, Scopus)

5. A Novel Splice Site Variant in KLHL40 Gene in Multiple Affected NEM8 Family Members Who Present Phenotypic Variability

Sönmez B., KOCABEY M., POLAT A. İ., GÜRSOY S., KARAOĞLU P., Horvath R., et al.

Molecular Syndromology , cilt.16, sa.1, ss.61-68, 2025 (SCI-Expanded, Scopus)

6. Nusinersen for children with type I spinal muscular atrophy: 4 years’ clinical experience in Turkish cohort

Gülşen M., Dursun O. B., TEKİN A., YÜKSEL D., DEMİR E., ÖZTÜRK G., et al.

Frontiers in Neurology , cilt.16, 2025 (SCI-Expanded, Scopus)

7. Clinical features and long-term follow-up of patients with West syndrome: 5-year developmental outcomes

Güzin Y., Pekuz S., KARAOĞLU P., İbiş İ. B. P., Kırkgöz H. H., Yavuz M., et al.

Trends in Pediatrics , cilt.5, sa.4, ss.157-164, 2024 (Scopus)

8. Therapeutic implications of etiology-specific diagnosis of early-onset developmental and epileptic encephalopathies (EO-DEEs): A nationwide Turkish cohort study

Kanmaz S., Tekgul H., Kayilioglu H., Atas Y., Kart P. O., Yildiz N., et al.

Seizure , cilt.123, ss.17-25, 2024 (SCI-Expanded, Scopus)

9. Development and psychometric evaluation of the Ketogenic Diet Management Scale for Children with Epilepsy-Parent Form

Ayar D., BEKTAŞ M., ÜNALP A., YILMAZ Ü., KOS F. M., Yavuz M., et al.

Children's Health Care , cilt.53, sa.3, ss.263-278, 2024 (SSCI, Scopus)

10. Optic neuritis in Turkish children and adolescents: A multicenter retrospective study

Direk M. Ç., Besen Ş., Öncel İ., GÜNBEY C., Özdoğan O., TEKİN ORGUN L., et al.

Multiple Sclerosis and Related Disorders , cilt.81, 2024 (SCI-Expanded, Scopus)

11. A multicenter study of radiologically isolated syndrome in children and adolescents: Can we predict the course?

Yılmaz D., Teber S., Gültutan P., YILDIRIM M., BEKTAŞ Ö., Alikılıç D., et al.

Multiple Sclerosis and Related Disorders , cilt.79, 2023 (SCI-Expanded, Scopus)

12. Retrospective evaluation of Guillain-Barre syndrome in children: A single-center experience

Güzin Y., YILMAZ Ü., Pekuz S., KARAOĞLU P., Parlak İbiş İ. B., Kırkgöz H. H., et al.

Pediatrics International , cilt.65, sa.1, 2023 (SCI-Expanded, Scopus)

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

YILMAZ Ü., Gücüyener K., Yavuz M., Öncel İ., CANPOLAT M., ÜNVER O., et al.

European Journal of Paediatric Neurology , cilt.41, ss.8-18, 2022 (SCI-Expanded, Scopus)

14. Psychometric properties of the Turkish version of the Epilepsy Disclosure Scale – Youth and Parent Versions

Ayar D., ÜNALP A., YILMAZ Ü., BEKTAŞ M., KARAOĞLU P., Akçay E., et al.

Epilepsy and Behavior , cilt.134, 2022 (SCI-Expanded, Scopus)

15. Benefits of ketogenic diet in a pediatric patient with Ehlers-Danlos syndrome and STXBP1-related epileptic encephalopathy

ÜNALP A., Gazeteci Tekin H., KARAOĞLU P., Akışın Z.

International Journal of Neuroscience , cilt.132, sa.9, ss.950-952, 2022 (SCI-Expanded, Scopus)

16. A rare case of hypomyelinating leukodystrophy-14 benefiting from ketogenic diet therapy

ÜNALP A., Köse M., KARAOĞLU P., Güzin Y., YILMAZ Ü.

Turkish Journal of Pediatrics , cilt.64, sa.4, ss.747-753, 2022 (SCI-Expanded, Scopus, TRDizin)

17. Evaluation of Quality of Life and Psychiatric Aspects of Children with Epilepsy and Their Families Using Self-assessment Questionnaires

ÜNALP A., KUTLU A., KARAOĞLU P., YILMAZ Ü., Çakaloz B.

Turkish Archives of Pediatrics , cilt.57, sa.3, ss.282-289, 2022 (Scopus, TRDizin)

18. Psychometric properties of a Turkish version of the quality of life in childhood epilepsy questionnaire

AYAR D., ÜNALP A., BEKTAŞ M., YILMAZ Ü., KARAOĞLU P., KOS F. M.

Journal of Pediatric Nursing , cilt.62, ss.91-97, 2022 (SCI-Expanded, SSCI, Scopus)

19. Clinical and electrophysiological prognostic factors of childhood absence epilepsy

Tekin H. G., KARAOĞLU P., Edem P.

Journal of Pediatric Research , cilt.8, sa.3, ss.320-325, 2021 (ESCI, Scopus, TRDizin)

20. The utility of next-generation sequencing technologies in diagnosis of Mendelian mitochondrial diseases and reflections on clinical spectrum

Kose M., Isik E., Aykut A., Durmaz A., KÖSE E., Ersoy M., et al.

Journal of Pediatric Endocrinology and Metabolism , cilt.34, sa.4, ss.417-430, 2021 (SCI-Expanded, Scopus)

21. Neuronal ceroid lipofuscinosis: genetic and phenotypic spectrum of 14 patients from Turkey

Kose M., KÖSE E., ÜNALP A., YILMAZ Ü., Edizer S., Tekin H. G., et al.

Neurological Sciences , cilt.42, sa.3, ss.1103-1111, 2021 (SCI-Expanded, Scopus)

22. Expanding the spectrum of VAC14 related pediatric-onset neurological disease; striatonigral degeneration with brainstem involvement

KARAOĞLU P., Köse M.

European Journal of Medical Genetics , cilt.64, sa.1, 2021 (SCI-Expanded, Scopus)

Doç. Dr. Pakize KARAOĞLU

Yayınlar & Eserler

1. Ultrasonographic assessment of subarachnoid space width in healthy infants aged 0–3 months: normative data and associations with anthropometric parameters

2. The efficacy and tolerability of lacosamide adjunctive therapy in children with drug-refractory epilepsy: A nationwide Turkish cohort study

3. Electroencephalogram abnormalities in children presenting with language development delay

4. The Clinical and Molecular Spectrum of Patients With X-Linked Intellectual Disability and Novel Variations in Different Genes

5. A Novel Splice Site Variant in KLHL40 Gene in Multiple Affected NEM8 Family Members Who Present Phenotypic Variability

6. Nusinersen for children with type I spinal muscular atrophy: 4 years’ clinical experience in Turkish cohort

7. Clinical features and long-term follow-up of patients with West syndrome: 5-year developmental outcomes

8. Therapeutic implications of etiology-specific diagnosis of early-onset developmental and epileptic encephalopathies (EO-DEEs): A nationwide Turkish cohort study

9. Development and psychometric evaluation of the Ketogenic Diet Management Scale for Children with Epilepsy-Parent Form

10. Optic neuritis in Turkish children and adolescents: A multicenter retrospective study

11. A multicenter study of radiologically isolated syndrome in children and adolescents: Can we predict the course?

12. Retrospective evaluation of Guillain-Barre syndrome in children: A single-center experience

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

14. Psychometric properties of the Turkish version of the Epilepsy Disclosure Scale – Youth and Parent Versions

15. Benefits of ketogenic diet in a pediatric patient with Ehlers-Danlos syndrome and STXBP1-related epileptic encephalopathy

16. A rare case of hypomyelinating leukodystrophy-14 benefiting from ketogenic diet therapy

17. Evaluation of Quality of Life and Psychiatric Aspects of Children with Epilepsy and Their Families Using Self-assessment Questionnaires

18. Psychometric properties of a Turkish version of the quality of life in childhood epilepsy questionnaire

19. Clinical and electrophysiological prognostic factors of childhood absence epilepsy

20. The utility of next-generation sequencing technologies in diagnosis of Mendelian mitochondrial diseases and reflections on clinical spectrum

21. Neuronal ceroid lipofuscinosis: genetic and phenotypic spectrum of 14 patients from Turkey

22. Expanding the spectrum of VAC14 related pediatric-onset neurological disease; striatonigral degeneration with brainstem involvement

Yayın

Yayın (WoS)

Yayın (Scopus)

H-İndeks (WoS)

Atıf (Scopus)

H-İndeks (Scopus)

Atıf (TrDizin)

H-İndeks (TrDizin)

Atıf (Diğer Toplam)

Açık Erişim