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Arzu Ekici
ORCID
Publication Activity (10 Years)
Years Active: 2020-2022
Publications (10 Years): 8
Top Topics
Dna Methylation
Late Onset
Genome Wide Analysis
Cerebrospinal Fluid
Top Venues
Metabolic brain disease
Fetal and pediatric pathology
Neurological research
Arquivos de neuro-psiquiatria
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This page only lists publications with an associated author ORCID identifier.
Publications
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Ahmet Burak Civan
,
Arzu Ekici
,
Cengiz Havali
,
Nevin Kiliç
,
Muharrem Bostanci
Evaluation of the risk factors for recurrence and the development of epilepsy in patients with febrile seizure.
Arquivos de neuro-psiquiatria
80 (8) (2022)
Cengiz Havali
,
Arzu Ekici
,
Sevil Dorum
,
Özlem Görükmez
,
Ali Topak
Recently defined epileptic encephalopathy related to WWOX gene mutation: six patients and new mutations.
Neurological research
43 (9) (2021)
Arzu Ekici
,
Busra Caglar
,
Özlem Kara
,
Arzu Oto
,
Nevin Kiliç
Rare causes of anisocoria: Ipratropium bromide and Angel's trumpet.
Northern clinics of Istanbul
8 (6) (2021)
Cengiz Havali
,
Hülya İnce
,
Elif Başaran Gündoğdu
,
Esra Gürkaş
,
Yasemin Karal
,
Arzu Ekici
,
Ercan Gündoğdu
The management of elevated intracranial pressure and sinus vein thrombosis associated with mastoiditis: the experience of eighteen patients.
Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
(2021)
Pelin Teke Kisa
,
Gonca Kilic Yildirim
,
Burcu Ozturk Hismi
,
Sevil Dorum
,
Özge Yılmaz Küsbeci
,
Ali Topak
,
Figen Baydan
,
Fatma Nazlı Durmaz Celik
,
Orhan Görükmez
,
Zumrut Arslan Gulten
,
Arzu Ekici
,
Serhat Ozkan
,
Aylin Yaman
,
Nur Arslan
Patients with cerebrotendinous xanthomatosis diagnosed with diverse multisystem involvement.
Metabolic brain disease
36 (6) (2021)
Cengiz Havali
,
Sevil Dorum
,
Arzu Ekici
,
Özlem Görükmez
Approaches for diagnosis and treatment in neurotransmitter disorders of childhood.
Metabolic brain disease
36 (8) (2021)
Orhan Görükmez
,
Özlem Görükmez
,
Arzu Ekici
A Novel Nonsense FMN2 Mutation in Nonsyndromic Autosomal Recessive Intellectual Disability Syndrome.
Fetal and pediatric pathology
40 (6) (2020)
Özlem Kara
,
Orhan Görükmez
,
Arzu Ekici
,
Fatih Celik
A Novel Homozygous Mutation in CYP11A1 Gene is Associated with Severe Adrenal Insufficiency in 46, XX Patient.
Fetal and pediatric pathology
40 (5) (2020)