Doç. Dr. Cengiz Havalı

Reply to the Letter: "Uncovering the Missing Links: Autoimmunity and Infection in Pediatric Arterial Ischemic Stroke"

Arquivos de neuro-psiquiatria, 2026

DOI 10.1055/s-0046-1817047 PMID 41985495 Texte intégral en libre accèsSource : Europe PMC

Association of Inflammatory and Nutritional Biomarkers in Children with Febrile Seizures: A Case–Control Study of NLR, PNI, and CAR

Diagnostics, 2026

DOI 10.3390/diagnostics16162541 PMID 42650945 Texte intégral en libre accèsSource : ORCID

Psychiatric comorbidity may affect the quality of life in pediatric migraine patients, independently of pain frequency and PedMIDAS score

Neurology Asia, 2026

DOI 10.54029/2026xix Texte intégral en libre accèsSource : ORCID

Circulating Neurogranin and Calmodulin Levels in Children with Epilepsy: A Prospective Case–Control Study

SSRN Electronic Journal, 2026

DOI 10.2139/ssrn.7635731 Texte intégral en libre accèsSource : ORCID

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

Neuromuscular Disorders, 2026

DOI 10.1016/j.nmd.2026.107399 PMID 42727323 1 citation (OpenAlex) Source : OpenAlex

Acute Disseminated Encephalomyelitis in Children and Adolescents: A Multicenter Retrospective Study of Relapse and Outcome

Journal of Child Neurology, 2025

DOI 10.1177/08830738251334219 PMID 40340642 Source : OpenAlex

Central nervous system complications during treatment in childhood acute leukemia

Acta Neurologica Belgica, 2025

DOI 10.1007/s13760-024-02602-0 PMID 39192159 1 citation (Europe PMC) Texte intégral en libre accèsSource : ORCID

Acute arterial ischemic stroke in children: single-center experience

Arquivos de neuro-psiquiatria, 2025

DOI 10.1055/s-0045-1809661 PMID 40562371 1 citation (Europe PMC) Texte intégral en libre accèsSource : Europe PMC

Psychiatric Comorbidity May Affect the Quality of Life in Pediatric Migraine Patients, Independently of Pain Frequency and Pedmidas Score

2025

DOI 10.2139/ssrn.5224649 Source : ORCID

Acute necrotizing encephalopathy associated with RANBP2 mutation: value of MRI findings for diagnosis and intervention

Acta Neurologica Belgica, 2023

DOI 10.1007/s13760-022-02166-x PMID 36572756 9 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

Acute disseminated encephalomyelitis (ADEM) in children: a multicenter retrospective study

Kocaeli Üniversitesi - AVESİS, 2022

Source : OpenAlex

Evaluation of the risk factors for recurrence and the development of epilepsy in patients with febrile seizure

Arquivos de neuro-psiquiatria, 2022

DOI 10.1055/s-0042-1755202 PMID 36252585 6 citations (Europe PMC) Texte intégral en libre accèsSource : Europe PMC

Clinical, radiological, and genetic variation in pontocerebellar hypoplasia disorder and our clinical experience

Italian Journal of Pediatrics, 2022

DOI 10.1186/s13052-022-01349-9 PMID 36076253 15 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

Üre döngüsü bozuklukları klinik, laboratuvar ve genetik özellikleri: Tek merkez deneyimi

Mustafa Kemal Üniversitesi Tıp Dergisi, 2022

DOI 10.17944/mkutfd.998813 1 citation (OpenAlex) Texte intégral en libre accèsSource : ORCID

The management of elevated intracranial pressure and sinus vein thrombosis associated with mastoiditis: the experience of eighteen patients

Child's Nervous System, 2022

DOI 10.1007/s00381-021-05402-6 PMID 34713346 5 citations (Europe PMC) Source : ORCID

Newly defined peroxisomal disease with novel ACBD5 mutation

Journal of Pediatric Endocrinology and Metabolism, 2022

DOI 10.1515/jpem-2020-0352 PMID 34668366 10 citations (Europe PMC) Source : ORCID

Ailelere ve Birinci Basamakta Sağlık Çalışanlarına Yönelik Çocuk Nöroloji

Akademisyen Kitabevi eBooks, 2022

DOI 10.37609/akya.1401 Texte intégral en libre accèsSource : OpenAlex

Outcomes of Inpatient Child Neurology Consultations

OSMANGAZİ JOURNAL OF MEDICINE, 2021

DOI 10.20515/otd.1017060 Texte intégral en libre accèsSource : OpenAlex

Approaches for diagnosis and treatment in neurotransmitter disorders of childhood

Metabolic Brain Disease, 2021

DOI 10.1007/s11011-021-00838-w PMID 34550503 2 citations (Europe PMC) Source : ORCID

Çocuklarda Kortikal Gelişimsel Malformasyonlara Tanısal Yaklaşım: 36 Hastanın Klinik, Görüntüleme ve Laboratuvar Verileri

Turkish Journal of Pediatric Disease, 2021

DOI 10.12956/tchd.899026 Texte intégral en libre accèsSource : ORCID

Recently defined epileptic encephalopathy related to WWOX gene mutation: six patients and new mutations

Neurological Research, 2021

DOI 10.1080/01616412.2021.1932173 PMID 34034642 5 citations (Europe PMC) Source : ORCID

Case series of Arginase 1 deficiency: Expanding the spectrum in hyperargininemia

Pediatrics International, 2021

DOI 10.1111/ped.14945 PMID 34343381 2 citations (Europe PMC) Source : ORCID

The Diagnostic Evaluation of Patients with Hereditary Ataxia in Children: Thirteen Patients and Comprehensive Approach

Mustafa Kemal Üniversitesi Tıp Dergisi, 2021

DOI 10.17944/mkutfd.919601 Texte intégral en libre accèsSource : ORCID

Magnetic resonance imaging patterns of subacute sclerosing panencephalitis may mimic metabolic disorders: clinical, electroencephalographic and imaging features of six cases

Acta Neurologica Belgica, 2021

DOI 10.1007/s13760-020-01469-1 PMID 32809122 5 citations (Europe PMC) Source : ORCID

Rarely Seen Poland–Moebius Syndrome: A Comprehensive View with Perspective of Pediatric Neurology

Journal of Pediatric Neurology, 2020

DOI 10.1055/s-0039-1691779 1 citation (OpenAlex) Source : ORCID

Two different missense mutations of PEX genes in two similar patients with severe Zellweger syndrome: an argument on the genotype-phenotype correlation

Journal of Pediatric Endocrinology and Metabolism, 2020

DOI 10.1515/jpem-2019-0194 PMID 32069232 4 citations (Europe PMC) Source : ORCID

A rare pediatric case of neurobrucellosis with bilateral optic neuritis

Turkish Journal of Pediatrics, 2020

DOI 10.24953/turkjped.2020.06.023 PMID 33372450 5 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

Cerebral neoplasm in L-2-hydroxyglutaric aciduria: two different presentations

Child's Nervous System, 2020

DOI 10.1007/s00381-019-04466-9 PMID 31858216 6 citations (Europe PMC) Source : ORCID

MRI in CLN2 disease patients: Subtle features that support an early diagnosis

European Journal of Paediatric Neurology, 2020

DOI 10.1016/j.ejpn.2020.07.009 PMID 32855042 9 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

Two patients with glutaric aciduria type 3: A novel mutation and brain magnetic resonance imaging findings

Turkish Journal of Pediatrics, 2020

DOI 10.24953/turkjped.2020.04.017 PMID 32779420 10 citations (Europe PMC) Texte intégral en libre accèsSource : ORCID

Novel MECR Mutation in Childhood-Onset Dystonia, Optic Atrophy, and Basal Ganglia Signal Abnormalities

Neuropediatrics, 2019

DOI 10.1055/s-0039-1688767 PMID 31137067 13 citations (Europe PMC) Source : ORCID

Temporary seizure in an infant who had been exposed to g-amino butyric acid receptor antagonist thiocolchicoside

Pediatric Emergency Care, 2019

DOI 10.1097/pec.0000000000001161 PMID 28486264 2 citations (Europe PMC) Source : ORCID

A child with atypically subtle clinical presentation of acute arterial ischaemic stroke in the middle cerebral artery

Interventional Neuroradiology, 2018

DOI 10.1177/1591019918790241 PMID 30033787 1 citation (Europe PMC) Texte intégral en libre accèsSource : ORCID

Are diagnostic magnetic resonance patterns life-saving in children with biotin-thiamine-responsive basal ganglia disease?

European Journal of Paediatric Neurology, 2018

DOI 10.1016/j.ejpn.2018.06.009 PMID 30054086 6 citations (Europe PMC) Source : ORCID

Nöronal seroid lipofuksinozis tanılı hastalarda klinik ve genetik özelliklerinin değerlendirilmesi

Kocaeli Üniversitesi - AVESİS, 2018

Source : OpenAlex

The efficacy of orbital ultrasonography and magnetic resonance imaging findings with direct measurement of intracranial pressure in distinguishing papilledema from pseudopapilledema

Child's Nervous System, 2017

DOI 10.1007/s00381-017-3454-6 PMID 28534259 13 citations (Europe PMC) Source : ORCID

Two cases of levetiracetam overdose without any serious side effects

Gazi Medical Journal, 2017

DOI 10.12996/gmj.2017.39 3 citations (OpenAlex) Texte intégral en libre accèsSource : ORCID

Spastic Paraplegia with SPG11 Gene delE39 in a Turkish Patient

Gazi Medical Journal, 2016

DOI 10.12996/gmj.2016.64 Texte intégral en libre accèsSource : ORCID

Ektopik Böbrek ve Dismorfik Bulguları Olan İnfantil Nöroaksonal Distrofi

Kocaeli Üniversitesi - AVESİS, 2016

Source : OpenAlex

Does nephrotoxicity exist in pediatric epileptic patients on valproate or carbamazepine therapy?

Journal of Child Neurology, 2015

DOI 10.1177/0883073814538505 PMID 24958008 9 citations (Europe PMC) Source : ORCID

Novel magnetic resonance imaging findings in children with intracranial hypertension

Pediatric Neurology, 2015

DOI 10.1016/j.pediatrneurol.2015.03.028 PMID 26101095 26 citations (Europe PMC) Source : ORCID

Increased Intracranial Hypertension in Children with Novel MRI Findings

2015

Source : OpenAlex

İnfeksiyonlar Tetiklenen Tekrarlayan Akut Nekrotizan Ensefalopati: RANBP2 Mutasyonu Saptanan Bir Olgu

Kocaeli Üniversitesi - AVESİS, 2015

Source : OpenAlex

Bilateral optik nörit tablosuyla başvuran bir Nörobruselloz vakası

Kocaeli Üniversitesi - AVESİS, 2015

Source : OpenAlex

Bir Moebius-Poland Sendromu

Kocaeli Üniversitesi - AVESİS, 2015

Source : OpenAlex

İNFEKSİYONLA TETİKLENEN TEKRARLAYAN AKUT NEKROTİZAN ENSEFALOPATİ: RANBP2 MUTASYONU SAPTANAN BİR OLGU

Kocaeli Üniversitesi - AVESİS, 2015

Source : OpenAlex

Enfeksiyonla tetiklenen tekrarlayan akut nekrotizan ensefalopati: RANBP2 mutasyonu saptanan bir olgu.

Kocaeli Üniversitesi - AVESİS, 2015

Source : OpenAlex

Arterial iskemik inmeli bir çocuk hastada atipik klinik prezentasyon

Kocaeli Üniversitesi - AVESİS, 2015

Source : OpenAlex

Herediter spastik paraparezi: SPG11 geninde mutasyon

Kocaeli Üniversitesi - AVESİS, 2015

Source : OpenAlex

Nadir görülen bir periodik aparalizi olgusu: Andersen- Tawil Sendromu

Kocaeli Üniversitesi - AVESİS, 2015

Source : OpenAlex