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1 . Academic Journal
Evaluation of seizure semiology, genetics, magnetic resonance imaging, and electroencephalogram findings in children with Rett syndrome: A multicenter retrospective study
저자
by
Yıldız, Nihal
;
Serdaroğlu, Esra
;
Kart, Pınar Özkan
;
Besen, Seyda
;
Kanmaz, Seda
, et al.
소스
In
Epilepsy Research
September 2024 205
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7 . Academic Journal
A Multicenter Study of Self-Limited Epilepsy With Centrotemporal Spikes: Effectiveness of Antiseizure Medication With Respect to Spike-Wave Index
저자
by
Dilber, Beril
;
Serdaroğlu, Esra
;
Kanmaz, Seda
;
Kılıç, Betül
;
İpek, Rojan
, et al.
소스
In
Pediatric Neurology
March 2024 152:79-86
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7 . Academic Journal
Optic neuritis in Turkish children and adolescents: A multicenter retrospective study
저자
by
Direk, Meltem Çobanoğulları
;
Besen, Şeyda
;
Öncel, İbrahim
;
Günbey, Ceren
;
Özdoğan, Orhan
, et al.
소스
In
Multiple Sclerosis and Related Disorders
January 2024 81
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7 . Academic Journal
The effectiveness and tolerability of clobazam in the pediatric population: Adjunctive therapy and monotherapy in a large-cohort multicenter study
저자
by
Kamaşak, Tülay
;
Serdaroğlu, Esra
;
Yılmaz, Özlem
;
Kılıç, Betül Aydın
;
Polat, Burçin G.
, et al.
소스
In
Epilepsy Research
August 2022 184
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7 . Academic Journal
A Homozygous Missense Variant in HSD17B4 Identified in Two Different Families.
저자
by
Özkan Kart, Pınar
;
Sahin, Yavuz
;
Yıldız, Nihal
;
Cebi, Alper Han
;
Esenulku, Gulnur
, et al.
소스
Molecular Syndromology; 2024, Vol. 15 Issue 2, p143-148, 6p
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7 . Academic Journal
The Impact of the COVID-19 Pandemic on the Educational Process of Children with Autism Spectrum Disorder and Effects on the Parental Quality of Life.
저자
by
YILDIZ, Nihal
;
ÖZEN, Nalan
;
ÖZKAN KART, Pınar
;
YILDIRIM, Selman
;
KARADENIZ, Serkan
, et al.
소스
Journal of Pediatric Disease / Türkiye Çocuk Hastalıkları Dergisi
. Jan2024, Vol. 18 Issue 1, p41-48. 8p.
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7 . Periodical
A Homozygous Missense Variant in HSD17B4Identified in Two Different Families
저자
by
Özkan Kart, Pınar
;
Sahin, Yavuz
;
Yıldız, Nihal
;
Cebi, Alper Han
;
Esenulku, Gulnur
, et al.
소스
Molecular Syndromology; March 2024, Vol. 15 Issue: 2 p143-148, 6p
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7 . Academic Journal
Multisystem Inflammatory Syndrom in a Child Presenting with Acute Hemiparesis as a Rare Neurologic Manifestation.
저자
by
YILDIZ, Nihal
;
GAYRETLİ AYDIN, Zeynep Gökçe
;
DİLBER, Beril
;
YEŞİLBAŞ, Osman
.
소스
Journal of Pediatric Disease / Türkiye Çocuk Hastalıkları Dergisi
. Mar2024, Vol. 18 Issue 2, p140-142. 3p.
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6 . Academic Journal
Shared Biological Pathways and Processes in Patients with Intellectual Disability: A Multicenter Study.
저자
by
Günay, Çağatay
;
Aykol, Duygu
;
Özsoy, Özlem
;
Sönmezler, Ece
;
Hanci, Yaren Sena
, et al.
소스
Neuropediatrics
. Aug2023, Vol. 54 Issue 4, p225-238. 14p.
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7 . Academic Journal
A novel INPP4A mutation with pontocerebellar hypoplasia, myoclonic epilepsy, microcephaly, and severe developmental delay.
저자
by
Özkan Kart, Pınar
;
Citli, Senol
;
Yildiz, Nihal
;
Cansu, Ali
.
소스
Brain & Development
. May2023, Vol. 45 Issue 5, p300-305. 6p.
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